CN105072902B - 除草组合物 - Google Patents
除草组合物 Download PDFInfo
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- CN105072902B CN105072902B CN201380073897.4A CN201380073897A CN105072902B CN 105072902 B CN105072902 B CN 105072902B CN 201380073897 A CN201380073897 A CN 201380073897A CN 105072902 B CN105072902 B CN 105072902B
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- Prior art keywords
- component
- composition
- herbicide
- methyl
- substitute
- Prior art date
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- 239000004009 herbicide Substances 0.000 claims description 247
- 150000003839 salts Chemical class 0.000 claims description 156
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- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 37
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- ILMHTGUGRLGMCR-LRIVTRFWSA-N 14-dihydroxycornestin Chemical compound CCC[C@H]1[C@H](O)C(=O)C[C@H](O)\C(=C/C)CC2=C1C(=O)OC2=O ILMHTGUGRLGMCR-LRIVTRFWSA-N 0.000 claims description 30
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
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- BWILYWWHXDGKQA-UHFFFAOYSA-M potassium propanoate Chemical compound [K+].CCC([O-])=O BWILYWWHXDGKQA-UHFFFAOYSA-M 0.000 description 1
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- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical class OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing carboxylic groups or thio analogues thereof, directly attached by the carbon atom to a cycloaliphatic ring; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/20—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom three- or four-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Abstract
提供了除草组合物,包含至少一种式(I)化合物和至少一种选自说明书中所列除草活性化合物的其他化合物,其中R1、R2和R3如说明书中所定义。
Description
本发明涉及包含至少一种式I化合物和至少一种选自除草活性化合物的其他化合物的除草组合物。
在作物保护组合物的情况下,原则上希望提高活性化合物的特异性活性和效果的可靠性。特别希望作物保护组合物有效防治有害植物,但同时与所述有用植物相容。还希望宽活性谱,允许同时防治有害植物。通常而言,这不能使用单一除草活性化合物实现。
使用许多高度有效的除草剂,存在的问题是它们与有用植物,尤其是双子叶农作物,如棉花、油籽油菜以及禾本科植物,如大麦、小米、玉米、稻、小麦和甘蔗的相容性并不总是令人满意,即除了有害植物外,农作物也以不能容忍的程度受损。通过降低施用率,不损伤有用植物;然而,自然也降低了防治有害植物的程度。
通常而言,问题是除草剂仅可在窄时间范围内施用以实现所需除草作用,该时间范围可能不可预测地受气候条件影响。
已知不同呈特异性活性的除草剂的特殊组合以协同增效效果导致除草剂组分的活性增强。以此方式可以降低防治有害植物所需除草活性化合物的施用率。
此外,已知在一些情况下联合施用特异性起作用的除草剂和有机活性化合物—其中一些也可能具有除草活性—允许实现更好的农作物相容性。在这些情况下,活性化合物起解毒剂或拮抗剂作用且也称为安全剂,因为它们降低或者甚至防止对农作物的损害。
Cornexistin(I.a1)及其相应二元酸(I.a2)由EP-A 0 290 193已知:
羟基cornexistin(I.a3)及其相应二元酸(I.a4)由US 5,424,278已知:
这些化合物的除草活性也由引用的参考文献已知。JP-A 1990-256 602公开了cornexistin(I.a1)及其二元酸(I.a2)与某些除草剂的混合物。
然而,例如就已知除草组合物的活性、活性范围和与有用植物的相容性而言仍有改进空间。
本发明的目的是要提供对不希望的有害植物具有高度活性的除草组合物。同时,该组合物应与有用植物具有良好相容性。此外,本发明组合物应具有宽活性谱。本发明的另一目的是降低活性成分的施用率。
该目的和其他目的由下面的除草组合物实现。
因此,在本发明的一方面提供了一种除草组合物,其包含:
A)至少一种式I的除草活性化合物(除草剂A):
其中
R1为CH3或CH2OH,以及
R2和R3与相邻碳原子一起形成二氢-2,5-二氧代呋喃环,或者
R2和R3为OH;
包括其可农用盐和衍生物;
以及
B)至少一种选自b1)-b15)组除草剂的其他活性化合物(除草剂B):
b1)ACC类脂生物合成抑制剂;
b3)光合成抑制剂PS I,
b4)原卟啉原-IX氧化酶抑制剂,
b5)漂白剂除草剂;
b6)烯醇丙酮酰莽草酸3-磷酸合成酶抑制剂(EPSP抑制剂);
b7)谷氨酰胺合成酶抑制剂;
b8)7,8-二氢蝶酸合成酶抑制剂(DHP抑制剂);
b11)纤维素生物合成抑制剂;
b12)去偶剂除草剂;
b13)植物生长素除草剂;
b14)植物生长素输送抑制剂;和
b15)选自溴丁酰草胺(bromobutide)、氯甲丹(chlorflurenol)、氯甲丹(chlorflurenol-methyl)、环庚草醚(cinmethylin)、香豆酮(coumaron)、苄草隆(cumyluron)、茅草枯(dalapon)、棉隆(dazomet)、苯敌快(difenzoquat)、苯敌快(difenzoquat-metilsulfate)、噻节因(dimethipin)、甲胂钠(DSMA)、香草隆(dymron)、草藻灭(endothal)及其盐、乙苯酰草(etobenzanid)、氟燕灵(flamprop)、氟燕灵(flamprop-isopropyl)、甲氟燕灵(flamprop-methyl)、强氟燕灵(flamprop-M-isopropyl)、麦草伏(flamprop-M-methyl)、抑草丁(flurenol)、抑草丁(flurenol-butyl)、调嘧醇(flurprimidol)、膦铵素(fosamine)、膦铵素(fosamine-ammonium)、茚草酮(indanofan)、indaziflam、抑芽丹(maleic hydrazide)、氟草磺(mefluidide)、威百亩(metam)、methiozolin(CAS 403640-27-7)、叠氮甲烷(methyl azide)、溴甲烷、methyl-daimuron、碘甲烷、甲胂一钠(MSMA)、油酸、氯嗪草(oxaziclomefone)、壬酸、稗草畏(pyributicarb)、灭藻醌(quinoclamine)、苯氧丙胺津(triaziflam)和6-氯-3-(2-环丙基-6-甲基苯氧基)-4-哒嗪醇(CAS 499223-49-3)的其他除草剂;
包括其可农用盐和衍生物。
本发明组合物适合直接或以适当配制的组合物(农业化学组合物)作为除草剂。本文所用术语“农业化学组合物”是指包含农药有效量的至少一种活性成分和至少一种常用于农业化学组合物的助剂的组合物。
本发明尤其涉及除草活性农业化学组合物形式的组合物,该除草活性农业化学组合物包含除草有效量的如上所定义的A)至少一种式I化合物(除草剂A)和B)至少一种选自b1)-b15)组除草剂的其他化合物(除草剂B),以及还有至少一种液体和/或固体载体和/或一种或多种表面活性剂和需要的话一种或多种常用于农业化学组合物的其他助剂。
本发明还涉及农业化学组合物形式的组合物,该农业化学组合物为包含至少一种除草剂A和至少一种选自除草剂B的其他活性化合物以及至少一种固体或液体载体和/或一种或多种表面活性剂和需要的话一种或多种常用于农业化学组合物的其他助剂的单组分组合物。
本发明还涉及农业化学组合物形式的组合物,该农业化学组合物为包含含有至少一种除草剂A、固体或液体载体和/或一种或多种表面活性剂的第一组分,含有至少一种除草剂B、固体或液体载体和/或一种或多种表面活性剂的第二组分的双组分组合物,其中这两种组分还可以额外包含常用于农业化学组合物的其他助剂。
惊人的是,本发明包含至少一种除草剂A和至少一种除草剂B的组合物与基于对单独化合物观察到的除草活性所预期的相比具有更好的除草活性,即对有害植物的更好活性,或者更宽的活性谱。对基于单独化合物的混合物预期的除草活性可以使用Colby公式(见下文)计算。若观察到的活性超过单独化合物的预期加和活性,则存在协同增效现象。
此外,可以实现所需除草作用的时间范围可以通过本发明包含至少一种除草剂A和至少一种除草剂B以及任选如下所定义的安全剂C的组合物扩展。这与单独化合物相比允许更灵活地控时施用本发明组合物。
安全剂是防止或降低对有用植物的损害但不对除草活性组分对不希望的植物的除草作用具有显著影响的化合物。安全剂可以在播种之前施用(例如种子处理)、在枝或秧苗上施用以及在有用植物的出苗前或出苗后处理及其生长地中施用。
本发明包含至少一种除草剂A和至少一种如下所定义的安全剂C二者的组合物也对有害植物具有良好除草活性且对有用植物具有更好相容性。
惊人的是,本发明包含至少一种除草剂A、至少一种除草剂B和至少一种安全剂C的组合物与基于对单独化合物观察到的除草活性所预期的相比具有更好的除草活性,即对有害植物的更好活性,或者更宽的活性谱,并且比仅包含一种除草剂A和一种除草剂B的组合物相比对有用植物显示出更好的相容性。
因此,在本发明的一个实施方案中,该组合物包含至少一种除草剂A、至少一种除草剂B和至少一种安全剂C。
合适安全剂C的实例是解草酮(benoxacor)、喹氧乙酸(cloquintocet)、抑害腈(cyometrinil)、cyprosulfamide、抑害胺(dichlormid)、dicyclonon、dietholate、解草唑(fenchlorazole)、解草啶(fenclorim)、解草安(flurazole)、肟草安(fluxofenim)、解草呋(furilazole)、双苯唑酸(isoxadifen)、吡咯二酸(mefenpyr)、mephenate、萘二甲酸酐、解草腈(oxabetrinil)、4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷(MON4660,CAS 71526-07-3)、2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷(R-29148,CAS 52836-31-4)和N-(2-甲氧基苯甲酰基)-4-[(甲基氨基羰基)氨基]苯磺酰胺(CAS 129531-12-0)。
安全剂C、除草剂A和除草剂B可以同时或依次施用。
此外,本发明涉及一种包含除草活性量的至少一种本发明组合物和至少一种惰性液体和/或固体载体和合适的话至少一种表面活性物质的除草配制剂。
制备上述除草活性配制剂的方法也为本发明主题,该方法包括混合除草活性量的至少一种本发明除草组合物和至少一种惰性液体和/或固体载体和合适的话至少一种表面活性物质。
此外,本发明涉及一种防治不希望的植物生长的方法,尤其是在农作物栽培时防治不希望的植物生长的方法。
本发明尤其涉及一种防治不希望的植物生长的方法,包括使除草活性量的至少一种本发明除草组合物作用于植物、其环境或种子上。
本发明还涉及一种使植物干燥或脱叶的方法。
本文所用术语“不希望的植物生长”和“有害植物”是同义词。
术语“cornexistin”是指式(I.a1)化合物及其可农用盐。
术语“cornexistin的二元酸”是指式(I.a2)化合物及其可农用盐。
术语“羟基cornexistin”是指式(I.a3)化合物及其可农用盐。
术语“羟基cornexistin的二元酸”是指式(I.a4)化合物及其可农用盐。
本文所述式(I.a1)-(I.a4)化合物能够形成几何异构体,例如E/Z异构体。因此,术语“cornexistin”、“cornexistin的二元酸”、“羟基cornexistin”和“羟基cornexistin的二元酸”还包括纯E或Z异构体及其混合物。
术语“可农用盐”在本文通常用于指其阳离子和阴离子分别对cornexistin的二元酸和羟基cornexistin的二元酸的除草活性没有不利影响的那些阳离子的盐和那些酸的酸加成盐。
优选的阳离子是碱金属的离子,优选锂、钠和钾离子,碱土金属的离子,优选钙和镁离子,以及过渡金属的离子,优选锰、铜、锌和铁离子,此外还有铵和其中1-4个氢原子被C1-C4烷基、羟基-C1-C4烷基、C1-C4烷氧基-C1-C4烷基、羟基-C1-C4烷氧基-C1-C4烷基、苯基或苄基替代的取代铵,优选铵、甲基铵、异丙基铵、二甲基铵、二异丙基铵、三甲基铵、庚基铵、十二烷基铵、十四烷基铵、四甲基铵、四乙基铵、四丁基铵、2-羟基乙基铵(醇胺盐)、2-(2-羟基乙-1-氧基)乙-1-基铵(二甘醇胺盐)、二(2-羟基乙-1-基)铵(=二醇胺盐)、三(2-羟基乙基)铵(=三醇胺盐)、三(2-羟基丙基)铵、苄基三甲基铵、苄基三乙基铵、N,N,N-三甲基乙醇铵(胆碱盐),此外还有离子,锍离子,优选三(C1-C4烷基)锍,如三甲基锍,以及氧化锍离子,优选三(C1-C4烷基)氧化锍,最后还有多元胺的盐如N,N-二(3-氨基丙基)甲基胺和二亚乙基三胺。
有用酸加成盐的阴离子主要是氯离子、溴离子、氟离子、碘离子、硫酸氢根、甲基硫酸根、硫酸根、磷酸二氢根、磷酸氢根、硝酸根、碳酸氢根、碳酸根、六氟硅酸根、六氟磷酸根、苯甲酸根以及C1-C4链烷酸的阴离子,优选甲酸根、乙酸根、丙酸根和丁酸根。
若本文所述除草化合物B和/或D和/或安全剂C能够形成几何异构体,例如E/Z异构体,则在本发明组合物中可以使用纯异构体及其混合物二者。若本文所述除草化合物B和/或D和/或安全剂C具有一个或多个手性中心并且因此作为对映体或非对映体存在,则在本发明组合物中可以使用纯对映体和非对映体及其混合物二者。若本文所述除草化合物B和/或D和/或安全剂C具有可离子化官能基团,则它们还可以以其可农用盐形式使用。合适的通常是其阳离子和阴离子分别对活性化合物的活性没有不利影响的那些阳离子的盐和那些酸的酸加成盐。
优选的阳离子和阴离子是对式I化合物所列那些。
本文所述具有羧基、羟基和/或氨基的除草化合物A、B和/或D和/或安全剂C能够直接使用或者以上述可农用盐形式或以可农用衍生物形式使用,例如以酰胺,如单-和二-C1-C6烷基酰胺或芳基酰胺,酯,例如烯丙基酯、炔丙基酯、C1-C10烷基酯、烷氧基烷基酯、四氢糠基(tefuryl)((四氢呋喃-2-基)甲基)酯以及还有硫酯,例如C1-C10烷基硫酯使用。优选的单-和二-C1-C6烷基酰胺是甲基和二甲基酰胺。优选的芳基酰胺例如是酰替苯胺和2-氯酰替苯胺。优选的烷基酯例如是甲基、乙基、丙基、异丙基、丁基、异丁基、戊基、异庚基(mexyl)(1-甲基己基)、甲庚基(meptyl)(1-甲基庚基)、庚基、辛基或异辛基(2-乙基己基)酯。优选的C1-C4烷氧基-C1-C4烷基酯是直链或支化C1-C4烷氧基乙基酯,例如2-甲氧基乙基、2-乙氧基乙基、2-丁氧基乙基(丁氧乙基(butotyl))、2-丁氧基丙基或3-丁氧基丙基酯。直链或支化C1-C10烷硫基酯的实例是乙硫基酯。
本发明的其他实施方案由权利要求书、说明书和实施例明了。应理解的是上面所述和下面仍待说明的本发明主题的特征在不背离本发明范围下不仅可以在每种特定情况下以给定组合应用,而且可以以其他组合应用。
下文所提到的本发明优选实施方案必须理解为相互独立地或者相互组合地是优选的。
优选活性成分A选自下列除草剂A:
a1)cornexistin(I.a1),
a2)cornexistin的二元酸(I.a2),
a3)羟基cornexistin(I.a3),
a4)羟基cornexistin的二元酸(I.a4),
a5)cornexistin(I.a1)和cornexistin的二元酸(I.a2)的混合物,
a6)羟基cornexistin(I.a3)和羟基cornexistin的二元酸(I.a4)的混合物,
a7)cornexistin(I.a1)和羟基cornexistin(I.a3)的混合物,
a8)cornexistin(I.a1)和羟基cornexistin的二元酸(I.a4)的混合物,
a9)cornexistin的二元酸(I.a2)和羟基cornexistin(I.a3)的混合物,
a10)cornexistin的二元酸(I.a2)和羟基cornexistin的二元酸(I.a4)的混合物,以及
a11)cornexistin(I.a1)、cornexistin的二元酸(I.a2)、羟基cornexistin(I.a3)和羟基cornexistin的二元酸(I.a4)的混合物,
包括其可农用盐和衍生物。
优选包含至少一种,优选正好一种除草剂A和至少一种除草剂B的本发明组合物。
进一步优选至少两种,优选正好两种除草剂A和至少一种除草剂B的本发明组合物。
在本发明的一个优选实施方案中,该组合物含有至少一种通过抑制乙酰基CoA羧化酶的类脂生物合成抑制剂(除草剂b1)(下文称为ACC除草剂)。ACC除草剂属于HRAC分类体系的A组。
根据本发明的另一实施方案,该组合物含有至少一种光合成抑制剂(除草剂b3),其使在植物中光合系统I中的电子转移(所谓的PSI抑制剂,HRAC分类的D组)转向并因此基于光合成的抑制。
根据本发明的另一实施方案,该组合物含有至少一种原卟啉原-IX氧化酶抑制剂(除草剂b4)。这些化合物的除草活性基于原卟啉原-IX氧化酶的抑制。这些抑制剂属于HRAC分类体系的E组。
根据本发明的另一实施方案,该组合物含有至少一种漂白剂除草剂(除草剂b5)。这些化合物的除草活性基于类胡萝卜素生物合成的抑制。这些包括通过抑制八氢番茄红素去饱和酶而抑制类胡萝卜素生物合成的化合物(所谓的PDS抑制剂,HRAC分类的F1组),抑制4-羟基苯基丙酮酸二加氧酶的化合物(HPPD抑制剂,HRAC分类的F2组),抑制DOX合成酶的化合物(HRAC分类的F4组)和通过未知作用方式抑制类胡萝卜素生物合成的化合物(漂白剂—未知目标,HRAC分类的F3组)。
根据本发明的另一实施方案,该组合物含有至少一种EPSP合成酶抑制剂(除草剂b6)。这些化合物的除草活性基于烯醇丙酮酰莽草酸3-磷酸合成酶的抑制并且因此基于植物中氨基酸生物合成的抑制。这些抑制剂属于HRAC分类体系的G组。
根据本发明的另一实施方案,该组合物含有至少一种谷氨酰胺合成酶抑制剂(除草剂b7)。这些化合物的除草活性基于谷氨酰胺合成酶的抑制并且因此基于植物中氨基酸生物合成的抑制。这些抑制剂属于HRAC分类体系的H组。
根据本发明的另一实施方案,该组合物含有至少一种DHP合成酶抑制剂(除草剂b8)。这些化合物的除草活性基于7,8-二氢蝶酸合成酶的抑制。这些抑制剂属于HRAC分类体系的I组。
根据本发明的另一实施方案,该组合物含有至少一种纤维素生物合成抑制剂(除草剂b11)。这些化合物的除草活性基于对纤维素生物合成的抑制并且因此基于植物中细胞壁合成的抑制。这些抑制剂属于HRAC分类体系的L组。
根据本发明的另一实施方案,该组合物含有至少一种去偶剂除草剂(除草剂b12)。这些化合物的除草活性基于细胞膜的干扰。这些抑制剂属于HRAC分类体系的M组。
根据本发明的另一实施方案,该组合物含有至少一种植物生长素除草剂(除草剂b13)。这些包括模拟植物生长素,即植物激素并影响植物生长的化合物。这些化合物属于HRAC分类体系的O组。
根据本发明的另一实施方案,该组合物含有至少一种植物生长素输送抑制剂(除草剂b14)。这些化合物的除草活性基于植物中植物生长素输送的抑制。这些化合物属于HRAC分类体系的P组。
根据本发明的另一实施方案,该组合物含有至少一种选自如下的其他除草剂(除草剂b15):溴丁酰草胺(bromobutide)、氯甲丹(chlorflurenol)、氯甲丹(chlorflurenol-methyl)、环庚草醚(cinmethylin)、苄草隆(cumyluron)、茅草枯(dalapon)、棉隆(dazomet)、苯敌快(difenzoquat)、苯敌快(difenzoquat-metilsulfate)、噻节因(dimethipin)、甲胂钠(DSMA)、香草隆(dymron)、草藻灭(endothal)及其盐、乙苯酰草(etobenzanid)、氟燕灵(flamprop)、氟燕灵(flamprop-isopropyl)、甲氟燕灵(flamprop-methyl)、强氟燕灵(flamprop-M-isopropyl)、麦草伏(flamprop-M-methyl)、抑草丁(flurenol)、抑草丁(flurenol-butyl)、调嘧醇(flurprimidol)、膦铵素(fosamine)、膦铵素(fosamine-ammonium)、茚草酮(indanofan)、抑芽丹(maleic hydrazide)、氟草磺(mefluidide)、威百亩(metam)、methiozolin(CAS 403640-27-7)、叠氮甲烷(methylazide)、溴甲烷、methyl-daimuron、碘甲烷、甲胂一钠(MSMA)、油酸、氯嗪草(oxaziclomefone)、壬酸、稗草畏(pyributicarb)、灭藻醌(quinoclamine)和6-氯-3-(2-环丙基-6-甲基苯氧基)-4-哒嗪醇(CAS 499223-49-3)。这些化合物具有未知作用模式且属于HRAC分类体系的Z组。
对于活性化合物的给定作用机理和分类,例如参见“HRAC,根据作用模式的除草剂分类”,(http://www.plantprotection.org/hrac/MOA.html)。
可以与除草剂A组合使用的除草剂B实例选自如下组:
b1)ACC类脂生物合成抑制剂:除草剂如枯杀达(alloxydim)、枯杀达(alloxydim-sodium)、丁氧环酮(butroxydim)、烯草酮(clethodim)、炔草酯(clodinafop)、炔草酯(clodinafop-propargyl)、噻草酮(cycloxydim)、氰氟草酯(cyhalofop)、氰氟草酯(cyhalofop-butyl)、氯甲草(diclofop)、氯甲草(diclofop-methyl)、唑禾草灵(fenoxaprop)、唑禾草灵(fenoxaprop-ethyl)、高唑禾草灵(fenoxaprop-P)、高唑禾草灵(fenoxaprop-P-ethyl)、吡氟禾草灵(fluazifop)、吡氟禾草灵(fluazifop-butyl)、精吡氟禾草灵(fluazifop-P)、精吡氟禾草灵(fluazifop-P-butyl)、吡氟氯禾灵(haloxyfop)、吡氟氯禾灵(haloxyfop-methyl)、精吡氟氯禾灵(haloxyfop-P)、精吡氟氯禾灵(haloxyfop-P-methyl)、唑酰草胺(metamifop)、唑啉草酯(pinoxaden)、环苯草酮(profoxydim)、喔草酯(propaquizafop)、喹禾灵(quizalofop)、喹禾灵(quizalofop-ethyl)、喹禾灵(四氢糠基酯)(quizalofop-tefuryl)、精喹禾灵(quizalofop-P)、精喹禾灵(quizalofop-P-ethyl)、精喹禾灵(四氢糠基酯)(quizalofop-P-tefuryl)、稀禾定(sethoxydim)、醌肟草(tepraloxydim)、肟草酮(tralkoxydim),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-72-6),4-(2',4'-二氯-4-环丙基[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-45-3),4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1033757-93-5),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-2,2,6,6-四甲基-2H-吡喃-3,5(4H,6H)-二酮(CAS 1312340-84-3),5-乙酰氧基-4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS1312337-48-6),5-乙酰氧基-4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮,5-乙酰氧基-4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1312340-82-1),5-乙酰氧基-4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1033760-55-2),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1312337-51-1),4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯,4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS1312340-83-2),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1033760-58-5)。
b3)PS I光合成抑制剂:例如敌草快(diquat)、敌草快(diquat-dibromide)、对草快(paraquat)、对草快(paraquat-dichloride)和对草快(paraquat-dimetilsulfate)。
b4)原卟啉原-IX氧化酶抑制剂:氟锁草醚(acifluorfen)、氟锁草醚(acifluorfen-sodium)、唑啶炔草(azafenidin)、bencarbazone、双苯嘧草酮(benzfendizone)、治草醚(bifenox)、氟丙嘧草酯(butafenacil)、氟酮唑草(carfentrazone)、氟酮唑草(carfentrazone-ethyl)、氯硝醚(chlomethoxyfen)、吲哚酮草酯(cinidon-ethyl)、氯氟草醚乙酯(ethoxyfen-ethyl)、异丙吡草酯(fluazolate)、氟哒嗪草酯(flufenpyr)、氟哒嗪草酯(flufenpyr-ethyl)、酰亚胺苯氧乙酸(flumiclorac)、酰亚胺苯氧乙酸戊酯(flumiclorac-pentyl)、氟嗪酮(flumioxazin)、乙羧氟草醚(fluoroglycofen)、乙羧氟草醚(fluoroglycofen-ethyl)、达草氟(fluthiacet)、达草氟(fluthiacet-methyl)、氟黄胺草醚(fomesafen)、氟硝磺酰胺(halosafen)、乳氟禾草灵(lactofen)、炔丙唑草(oxadiargyl)、恶草灵(oxadiazon)、乙氧氟草醚(oxyfluorfen)、戊唑草(pentoxazone)、氟唑草胺(profluazol)、双唑草腈(pyraclonil)、氟唑草酯(pyraflufen)、氟唑草酯(pyraflufen-ethyl)、苯嘧磺草胺(saflufenacil)、磺胺草唑(sulfentrazone)、噻二唑胺(thidiazimin)、[3-[2-氯-4-氟-5-(1-甲基-6-三氟甲基-2,4-二氧代-1,2,3,4-四氢嘧啶-3-基)苯氧基]-2-吡啶氧基]乙酸乙酯(CAS 353292-31-6)、N-乙基-3-(2,6-二氯-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 452098-92-9)、N-四氢糠基-3-(2,6-二氯-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 915396-43-9)、N-乙基-3-(2-氯-6-氟-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS452099-05-7)、N-四氢糠基-3-(2-氯-6-氟-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 45100-03-7)、3-[7-氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[1,4]嗪-6-基]-1,5-二甲基-6-硫代-[1,3,5]三嗪烷(triazinan)-2,4-二酮、1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS 1258836-72-4)、2-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-4,5,6,7-四氢异吲哚-1,3-二酮、1-甲基-6-三氟甲基-3-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-1H-嘧啶-2,4-二酮和(Z)-4-[2-氯-5-(4-氯-5-二氟甲氧基-1-甲基-1H-吡唑-3-基)-4-氟苯氧基]-3-甲基丁-2-烯酸甲酯;
b5)漂白剂除草剂:PDS抑制剂:氟丁酰草胺(beflubutamid)、吡氟草胺(diflufenican)、氟草同(fluridone)、氟咯草酮(flurochloridone)、呋草酮(flurtamone)、达草灭(norflurazon)、氟吡酰草胺(picolinafen)和4-(3-三氟甲基苯氧基)-2-(4-三氟甲基苯基)嘧啶(CAS 180608-33-7),HPPD抑制剂:苯并双环酮(benzobicyclon)、吡草酮(benzofenap)、异恶草酮(clomazone)、异氟草(isoxaflutole)、硝磺酮(mesotrione)、pyrasulfotole、吡唑特(pyrazolynate)、苄草唑(pyrazoxyfen)、磺草酮(sulcotrione)、tefuryltrione、tembotrione、topramezone和bicyclopyrone,漂白剂,未知目标:苯草醚(aclonifen)、杀草强(amitrole)和flumeturon;
b6)EPSP合成酶抑制剂:草甘膦(glyphosate)、草甘膦异丙胺盐(glyphosate-isopropylammonium)、草甘膦钾(glyposate-potassium)和草硫膦(glyphosate-trimesium)(sulfosate);
b7)谷氨酰胺合成酶抑制剂:双丙氨酰膦(bilanaphos(bialaphos))、双丙氨酰膦(bilanaphos-sodium)、草铵膦(glufosinate)、草铵膦(glufosinate-P)和草铵膦(glufosinate-ammonium);
b8)DHP合成酶抑制剂:黄草灵(asulam);
b11)纤维素生物合成抑制剂:草克乐(chlorthiamid)、敌草腈(dichlobenil)、胺草唑(flupoxam)、indaziflam、异恶草胺(isoxaben)、苯氧丙胺津(triaziflam)、三唑并甲酰胺(triazolocarboxamide)和1-环己基-5-五氟苯氧基-14-[1,2,4,6]硫杂三嗪-3-基胺;
b12)去偶剂除草剂:地乐酚(dinoseb)、地乐消酚(dinoterb)以及二硝甲酚(DNOC)及其盐;
b13)植物生长素除草剂:2,4-D及其盐和酯,如氯酰草膦(clacyfos),2,4-DB及其盐和酯,aminocyclopyrachlor及其盐和酯,氨草啶(aminopyralid)及其盐如氨草啶铵盐(aminopyralid-tris(2-hydroxypropyl)ammonium)及其酯,草除灵(benazolin),草除灵(benazolin-ethyl),草灭平(chloramben)及其盐和酯,稗草胺(clomeprop),二氯皮考啉酸(clopyralid)及其盐和酯,麦草畏(dicamba)及其盐和酯,2,4-滴丙酸(dichlorprop)及其盐和酯,高2,4-滴丙酸(dichlorprop-P)及其盐和酯,氟草烟(fluroxypyr),氟草烟(fluroxypyr-butometyl),氟氯胺啶(fluroxypyr-meptyl),氟氯吡啶酯(halauxifen)及其盐和酯(CAS 943832-60-8);MCPA及其盐和酯,2甲4氯乙硫酯(MCPA-thioethyl),MCPB及其盐和酯,2甲4氯丙酸(mecoprop)及其盐和酯,高2甲4氯丙酸(mecoprop-P)及其盐和酯,毒莠定(picloram)及其盐和酯,二氯喹啉酸(quinclorac),喹草酸(quinmerac),TBA(2,3,6)及其盐和酯以及定草酯(triclopyr)及其盐和酯;
b14)植物生长素输送抑制剂:二氟吡隆(diflufenzopyr)、二氟吡隆(diflufenzopyr-sodium)、抑草生(naptalam)和抑草生(naptalam-sodium);
b15)其他除草剂:溴丁酰草胺(bromobutide)、氯甲丹(chlorflurenol)、氯甲丹(chlorflurenol-methyl)、环庚草醚(cinmethylin)、苄草隆(cumyluron)、cyclopyrimorate(CAS 499223-49-3)及其盐和酯、茅草枯(dalapon)、棉隆(dazomet)、苯敌快(difenzoquat)、苯敌快(difenzoquat-metilsulfate)、噻节因(dimethipin)、甲胂钠(DSMA)、香草隆(dymron)、草藻灭(endothal)及其盐、乙苯酰草(etobenzanid)、氟燕灵(flamprop)、氟燕灵(flamprop-isopropyl)、甲氟燕灵(flamprop-methyl)、强氟燕灵(flamprop-M-isopropyl)、麦草伏(flamprop-M-methyl)、抑草丁(flurenol)、抑草丁(flurenol-butyl)、调嘧醇(flurprimidol)、膦铵素(fosamine)、膦铵素(fosamine-ammonium)、茚草酮(indanofan)、抑芽丹(maleic hydrazide)、氟草磺(mefluidide)、威百亩(metam)、methiozolin(CAS 403640-27-7)、叠氮甲烷(methyl azide)、溴甲烷、苯丙隆(methyl-dymron)、碘甲烷、甲胂一钠(MSMA)、油酸、氯嗪草(oxaziclomefone)、壬酸、稗草畏(pyributicarb)、灭藻醌(quinoclamine)和6-氯-3-(2-环丙基-6-甲基苯氧基)吡嗪-2-醇(CAS 499223-49-3)。
可以与本发明除草剂A组合使用的优选除草剂B选自如下组:
b1)ACC类脂生物合成抑制剂:烯草酮(clethodim)、炔草酯(clodinafop-propargyl)、噻草酮(cycloxydim)、氰氟草酯(cyhalofop-butyl)、氯甲草(diclofop-methyl)、高唑禾草灵(fenoxaprop-P-ethyl)、精吡氟禾草灵(fluazifop-P-butyl)、精吡氟氯禾灵(haloxyfop-P-methyl)、唑酰草胺(metamifop)、唑啉草酯(pinoxaden)、环苯草酮(profoxydim)、喔草酯(propaquizafop)、精喹禾灵(quizalofop-P-ethyl)、精喹禾灵(四氢糠基酯)(quizalofop-P-tefuryl)、稀禾定(sethoxydim)、醌肟草(tepraloxydim)、肟草酮(tralkoxydim),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-72-6),4-(2',4'-二氯-4-环丙基[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-45-3),4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1033757-93-5),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-2,2,6,6-四甲基-2H-吡喃-3,5(4H,6H)-二酮(CAS 1312340-84-3),5-乙酰氧基-4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1312337-48-6),5-乙酰氧基-4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮,5-乙酰氧基-4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1312340-82-1),5-乙酰氧基-4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1033760-55-2),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS1312337-51-1),4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯,4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1312340-83-2),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1033760-58-5);
b3)PS I光合成抑制剂:敌草快(diquat)、敌草快(diquat-dibromide)、对草快(paraquat)、对草快(paraquat-dichloride)、对草快(paraquat-dimetilsulfate)。
b4)原卟啉原-IX氧化酶抑制剂:氟锁草醚(acifluorfen-sodium)、bencarbazone、双苯嘧草酮(benzfendizone)、氟丙嘧草酯(butafenacil)、氟酮唑草(carfentrazone-ethyl)、吲哚酮草酯(cinidon-ethyl)、氟哒嗪草酯(flufenpyr-ethyl)、酰亚胺苯氧乙酸戊酯(flumiclorac-pentyl)、氟嗪酮(flumioxazin)、乙羧氟草醚(fluoroglycofen-ethyl)、氟黄胺草醚(fomesafen)、乳氟禾草灵(lactofen)、炔丙唑草(oxadiargyl)、恶草灵(oxadiazon)、乙氧氟草醚(oxyfluorfen)、戊唑草(pentoxazone)、氟唑草酯(pyraflufen-ethyl)、苯嘧磺草胺(saflufenacil)、磺胺草唑(sulfentrazone)、[3-[2-氯-4-氟-5-(1-甲基-6-三氟甲基-2,4-二氧代-1,2,3,4-四氢嘧啶-3-基)苯氧基]-2-吡啶氧基]乙酸乙酯(CAS 353292-31-6;S-3100)、N-乙基-3-(2,6-二氯-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 452098-92-9)、N-四氢糠基-3-(2,6-二氯-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 915396-43-9)、N-乙基-3-(2-氯-6-氟-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 452099-05-7)、N-四氢糠基-3-(2-氯-6-氟-4-三氟甲基苯氧基)-5-甲基-1H-吡唑-1-甲酰胺(CAS 45100-03-7)、3-[7-氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[1,4]嗪-6-基]-1,5-二甲基-6-硫代-[1,3,5]三嗪烷(triazinan)-2,4-二酮、1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS 1258836-72-4)、2-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-4,5,6,7-四氢异吲哚-1,3-二酮和1-甲基-6-三氟甲基-3-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-1H-嘧啶-2,4-二酮;
b5)漂白剂除草剂:苯草醚(aclonifen)、氟丁酰草胺(beflubutamid)、苯并双环酮(benzobicyclon)、异恶草酮(clomazone)、吡氟草胺(diflufenican)、氟咯草酮(flurochloridone)、呋草酮(flurtamone)、异氟草(isoxaflutole)、硝磺酮(mesotrione)、达草灭(norflurazon)、氟吡酰草胺(picolinafen)、pyrasulfotole、吡唑特(pyrazolynate)、磺草酮(sulcotrione)、tefuryltrione、tembotrione、topramezone、bicyclopyrone、4-(3-三氟甲基苯氧基)-2-(4-三氟甲基苯基)嘧啶(CAS 180608-33-7)、杀草强(amitrole)和flumeturon;
b6)EPSP合成酶抑制剂:草甘膦(glyphosate)、草甘膦异丙胺盐(glyphosate-isopropylammonium)、草甘膦钾(glyposate-potassium)和草硫膦(glyphosate-trimesium)(sulfosate);
b7)谷氨酰胺合成酶抑制剂:草铵膦(glufosinate)、草铵膦(glufosinate-P)、草铵膦(glufosinate-ammonium);
b8)DHP合成酶抑制剂:黄草灵(asulam);
b11)纤维素生物合成抑制剂:敌草腈(dichlobenil)、胺草唑(flupoxam)、indaziflam、异恶草胺(isoxaben)、苯氧丙胺津(triaziflam)和1-环己基-5-五氟苯氧基-14-[1,2,4,6]硫杂三嗪-3-基胺;
b12)去偶剂除草剂:地乐酚(dinoseb);
b13)植物生长素除草剂:2,4-D及其盐和酯,aminocyclopyrachlor及其盐和酯,氨草啶(aminopyralid)及其盐如氨草啶铵盐(aminopyralid-tris(2-hydroxypropyl)ammonium)及其酯,二氯皮考啉酸(clopyralid)及其盐和酯,麦草畏(dicamba)及其盐和酯,高2,4-滴丙酸(dichlorprop-P)及其盐和酯,氟氯胺啶(fluroxypyr-meptyl),氟氯吡啶酯(halauxifen)及其盐和酯(CAS 943832-60-8),MCPA及其盐和酯,MCPB及其盐和酯,高2甲4氯丙酸(mecoprop-P)及其盐和酯,毒莠定(picloram)及其盐和酯,二氯喹啉酸(quinclorac),喹草酸(quinmerac)以及定草酯(triclopyr)及其盐和酯;
b14)植物生长素输送抑制剂:二氟吡隆(diflufenzopyr)和二氟吡隆(diflufenzopyr-sodium);和
b15)其他除草剂:溴丁酰草胺(bromobutide)、环庚草醚(cinmethylin)、苄草隆(cumyluron)、cyclopyrimorate(CAS 499223-49-3)及其盐和酯、茅草枯(dalapon)、苯敌快(difenzoquat)、苯敌快(difenzoquat-metilsulfate)、甲胂钠(DSMA)、香草隆(dymron)(=daimuron)、氟燕灵(flamprop)、氟燕灵(flamprop-isopropyl)、甲氟燕灵(flamprop-methyl)、强氟燕灵(flamprop-M-isopropyl)、麦草伏(flamprop-M-methyl)、茚草酮(indanofan)、威百亩(metam)、溴甲烷、甲胂一钠(MSMA)、氯嗪草(oxaziclomefone)、壬酸和稗草畏(pyributicarb)。
可以与除草剂A组合使用的特别优选除草剂B选自如下组:
b1)ACC类脂生物合成抑制剂:炔草酯(clodinafop-propargyl)、噻草酮(cycloxydim)、氰氟草酯(cyhalofop-butyl)、高唑禾草灵(fenoxaprop-P-ethyl)、唑啉草酯(pinoxaden)、环苯草酮(profoxydim)、醌肟草(tepraloxydim)、肟草酮(tralkoxydim),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-72-6),4-(2',4'-二氯-4-环丙基[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1312337-45-3),4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5-羟基-2,2,6,6-四甲基-2H-吡喃-3(6H)-酮(CAS 1033757-93-5),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-2,2,6,6-四甲基-2H-吡喃-3,5(4H,6H)-二酮(CAS 1312340-84-3),5-乙酰氧基-4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1312337-48-6),5-乙酰氧基-4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮,5-乙酰氧基-4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS1312340-82-1),5-乙酰氧基-4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-3,6-二氢-2,2,6,6-四甲基-2H-吡喃-3-酮(CAS 1033760-55-2),4-(4'-氯-4-环丙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1312337-51-1),4-(2',4'-二氯-4-环丙基-[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯,4-(4'-氯-4-乙基-2'-氟[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1312340-83-2),4-(2',4'-二氯-4-乙基[1,1'-联苯]-3-基)-5,6-二氢-2,2,6,6-四甲基-5-氧代-2H-吡喃-3-基碳酸甲酯(CAS 1033760-58-5);
b3)PS I光合成抑制剂:对草快(paraquat)和对草快(paraquat-dichloride);
b4)原卟啉原-IX氧化酶抑制剂:氟酮唑草(carfentrazone-ethyl)、氟嗪酮(flumioxazin)、乳氟禾草灵(lactofen)、炔丙唑草(oxadiargyl)、乙氧氟草醚(oxyfluorfen)、苯嘧磺草胺(saflufenacil)、磺胺草唑(sulfentrazone)、[3-[2-氯-4-氟-5-(1-甲基-6-三氟甲基-2,4-二氧代-1,2,3,4-四氢嘧啶-3-基)苯氧基]-2-吡啶氧基]乙酸乙酯(CAS 353292-31-6;S-3100)、3-[7-氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[1,4]嗪-6-基]-1,5-二甲基-6-硫代-[1,3,5]三嗪烷(triazinan)-2,4-二酮、1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS 1258836-72-4)、2-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-4,5,6,7-四氢异吲哚-1,3-二酮和1-甲基-6-三氟甲基-3-(2,2,7-三氟-3-氧代-4-丙-2-炔基-3,4-二氢-2H-苯并[1,4]嗪-6-基)-1H-嘧啶-2,4-二酮;
b5)漂白剂除草剂:异恶草酮(clomazone)、吡氟草胺(diflufenican)、氟咯草酮(flurochloridone)、异氟草(isoxaflutole)、硝磺酮(mesotrione)、达草灭(norflurazone)、氟吡酰草胺(picolinafen)、磺草酮(sulcotrione)、tefuryltrione、tembotrione、topramezone、苯并双环酮(benzobicyclone)、bicyclopyrone、杀草强(amitrole)和flumeturon;
b6)EPSP合成酶抑制剂:草甘膦(glyphosate)、草甘膦异丙胺盐(glyphosate-isopropylammonium)和草硫膦(glyphosate-trimesium)(sulfosate);
b7)谷氨酰胺合成酶抑制剂:草铵膦(glufosinate)、草铵膦(glufosinate-P)和草铵膦(glufosinate-ammonium);
b8)DHP合成酶抑制剂:黄草灵(asulam);
b11)纤维素生物合成抑制剂:indaziflam、异恶草胺(isoxaben)、苯氧丙胺津(triaziflam)和三唑并甲酰胺(triazolocarboxamide);
b12)去偶剂除草剂:地乐酚(dinoseb);
b13)植物生长素除草剂:2,4-D及其盐和酯如氯酰草膦(clacyfos)、aminocyclopyrachlor及其盐和酯,氨草啶(aminopyralid)及其盐和酯,二氯皮考啉酸(clopyralid)及其盐和酯,麦草畏(dicamba)及其盐和酯,氟氯胺啶(fluroxypyr-meptyl),MCPA,二氯喹啉酸(quinclorac)和喹草酸(quinmerac);
b14)植物生长素输送抑制剂:二氟吡隆(diflufenzopyr)和二氟吡隆(diflufenzopyr-sodium);
b15)其他除草剂:香草隆(dymron)(=daimuron)、茚草酮(indanofan)、氯嗪草(oxaziclomefone)和壬酸。
可以与除草剂A组合使用的最优选除草剂B在下表1中给出:
表1
应理解的是任何具有羧基、氨基和/或羟基的除草剂B.1-B.39直接使用和/或以其可农用盐形式和/或以其可农用酯或酰胺形式使用。
根据本发明的优选实施方案,该组合物包含至少一种,优选正好一种除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少两种,优选正好两种相互不同的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少三种,优选正好三种相互不同的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种除草剂A和至少一种,优选正好一种除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种除草剂A和至少两种,优选正好两种相互不同的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种除草剂A和至少三种,优选正好三种相互不同的除草剂B。
根据本发明的一个优选实施方案,该组合物包含至少一种选自b1)、b3)、b4)、b5)、b6)、b7)、b8)、b11)、b12)、b13)、b14)和b15)组化合物,优选选自b1)、b3)、b4)、b5)、b6)、b7)、b8)、b11)、b12)、b13)、b14)或b15)组化合物的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种除草剂A,优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b1)组化合物,尤其选自烯草酮(B.1)、炔草酯(B.2)、噻草酮(B.3)、唑啉草酯(B.4)和稀禾定(B.5)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b3)组化合物,尤其是对草快及其可农用盐(B.6)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b4)组化合物,尤其选自氟酮唑草(B.7)、氟嗪酮(B.8)、乳氟禾草灵(B.9)、炔丙唑草(B.10)、乙氧氟草醚(B.11)、苯嘧磺草胺(B.12)、磺胺草唑(B.13)和1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS 1258836-72-4)(B.14)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b5)组化合物,优选选自苯并双环酮(B.15)、bicyclopyrone(B.16)、异恶草酮(B.17)、吡氟草胺(B.18)、异氟草(B.19)、硝磺酮(B.20)、达草灭(B.21)、氟吡酰草胺(B.22)、磺草酮(B.23)、tembotrione(B.24)和topramezone(B.25),尤其选自苯并双环酮(B.15)、异氟草(B.19)、硝磺酮(B.20)和topramezone(B.25)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b6)组化合物,尤其是草甘膦及其可农用盐(B.26)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b7)组化合物,尤其是草铵膦及其可农用盐(B.27)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少一种,优选正好一种选自b11)组化合物,尤其选自indaziflam(B.28)和异恶草胺(B.29)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少一种,优选正好一种选自b12)组化合物,尤其是地乐酚(B.30)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b13)组化合物,尤其选自2,4-D及其可农用盐(B.31)、麦草畏及其可农用盐(B.32)、氟草烟(B.33)、MCPA及其可农用盐(B.34)、喹草酸及其可农用盐(B.35)和二氯喹啉酸及其可农用盐(B.36)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b14)组化合物,尤其是二氟吡隆及其可农用盐(B.37)的除草剂B。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,以及至少一种,优选正好一种选自b15)组化合物,尤其选自香草隆(dymron)(=daimuron)(B.38)和壬酸及其可农用盐(B.39)的除草剂B。
在另一实施方案中,本发明组合物包含至少两种除草剂B,其中第一除草剂B选自b1)、b3)、b4)、b5)、b8)、b11)、b12、b13)、b14)和b15)组化合物,优选选自b1)、b3)、b4)、b5)、b8)、b11)、b12、b13)、b14或b15)组化合物,第二除草剂B选自b6)和b7)组化合物,优选选自b6)或b7)组化合物。
在本发明的另一实施方案中,本发明组合物包含至少一种选自a1)-a11)的除草剂A,至少一种除草剂B和至少一种安全剂C。
安全剂C的实例是解草酮(benoxacor)、喹氧乙酸(cloquintocet)、抑害腈(cyometrinil)、cyprosulfamide、抑害胺(dichlormid)、dicyclonon、dietholate、解草唑(fenchlorazole)、解草啶(fenclorim)、解草安(flurazole)、肟草安(fluxofenim)、解草呋(furilazole)、双苯唑酸(isoxadifen)、吡咯二酸(mefenpyr)、mephenate、萘二甲酸酐、解草腈(oxabetrinil)、4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷(MON4660,CAS 71526-07-3)、2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷(R-29148,CAS 52836-31-4)和N-(2-甲氧基苯甲酰基)-4-[(甲基氨基羰基)氨基]苯磺酰胺(CAS 129531-12-0)。
优选的安全剂C是解草酮(benoxacor)、喹氧乙酸(cloquintocet)、cyprosulfamide、抑害胺(dichlormid)、解草唑(fenchlorazole)、解草啶(fenclorim)、解草安(flurazole)、肟草安(fluxofenim)、解草呋(furilazole)、双苯唑酸(isoxadifen)、吡咯二酸(mefenpyr)、萘二甲酸酐、解草腈(oxabetrinil)、4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷(MON4660,CAS 71526-07-3)、2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷(R-29148,CAS 52836-31-4)和N-(2-甲氧基苯甲酰基)-4-[(甲基氨基羰基)氨基]苯磺酰胺(CAS 129531-12-0)。
特别优选的安全剂C是解草酮(benoxacor)、喹氧乙酸(cloquintocet)、cyprosulfamide、抑害胺(dichlormid)、解草唑(fenchlorazole)、解草啶(fenclorim)、解草呋(furilazole)、双苯唑酸(isoxadifen)、吡咯二酸(mefenpyr)、萘二甲酸酐、解草腈(oxabetrinil)、4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷(MON4660,CAS 71526-07-3)和2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷(R-29148,CAS 52836-31-4)。
最优选的安全剂C列于下表2中:
表2
应理解的是任何具有羧基、氨基和/或羟基的安全剂C.1-C.11直接使用和/或以其可农用盐形式使用。
根据本发明的一个优选实施方案,该组合物包含至少一种,优选正好一种除草剂B,以及至少一种,优选正好一种安全剂C。
根据本发明的另一优选实施方案,该组合物包含至少两种,优选正好两种相互不同的除草剂B,以及至少一种,优选正好一种安全剂C。
根据本发明的另一优选实施方案,该组合物包含至少三种,优选正好三种相互不同的除草剂B,以及至少一种,优选正好一种安全剂C。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种除草剂A,优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少一种,优选正好一种除草剂B,以及至少一种,优选正好一种安全剂C作为活性化合物。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少两种,优选正好两种相互不同的除草剂B,以及至少一种,优选正好一种安全剂C作为活性化合物。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少三种,优选正好三种相互不同的除草剂B,以及至少一种,优选正好一种安全剂C作为活性化合物。
根据本发明的另一优选实施方案,该组合物包含至少一种,优选正好一种优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)和a11),最优选选自a1)、a2)、a3)、a4)、a5)、a6)、a7)、a8)、a9)、a10)或a11)的除草剂A,至少一种,优选正好一种除草剂B,任选至少一种,优选正好一种安全剂C,以及至少一种,优选正好一种不同于除草剂A、B和C的其他除草剂D作为活性化合物。
合适除草剂D是选自如下组的除草剂:
d1)ALS抑制剂:
磺酰脲类如磺氨黄隆(amidosulfuron)、四唑黄隆(azimsulfuron)、苄嘧黄隆(bensulfuron)、苄嘧黄隆(bensulfuron-methyl)、氯嘧黄隆(chlorimuron)、氯嘧黄隆(chlorimuron-ethyl)、绿黄隆(chlorsulfuron)、醚黄隆(cinosulfuron)、环丙黄隆(cyclosulfamuron)、胺苯黄隆(ethametsulfuron)、胺苯黄隆(ethametsulfuron-methyl)、乙氧嘧黄隆(ethoxysulfuron)、啶嘧黄隆(flazasulfuron)、氟吡磺隆(flucetosulfuron)、氟定黄隆(flupyrsulfuron)、氟定黄隆(flupyrsulfuron-methyl-sodium)、甲酰氨磺隆(foramsulfuron)、吡氯黄隆(halosulfuron)、吡氯黄隆(halosulfuron-methyl)、啶咪黄隆(imazosulfuron)、碘黄隆(iodosulfuron)、碘甲黄隆钠(iodosulfuron-methyl-sodium)、iofensulfuron、iofensulfuron-sodium、甲基二磺隆(mesosulfuron)、metazosulfuron、甲黄隆(metsulfuron)、甲黄隆(metsulfuron-methyl)、烟嘧黄隆(nicosulfuron)、嘧苯胺磺隆(orthosulfamuron)、环丙氧黄隆(oxasulfuron)、氟嘧黄隆(primisulfuron)、氟嘧黄隆(primisulfuron-methyl)、propyrisulfuron、氟丙黄隆(prosulfuron)、吡嘧黄隆(pyrazosulfuron)、吡嘧黄隆(pyrazosulfuron-ethyl)、玉嘧黄隆(rimsulfuron)、嘧黄隆(sulfometuron)、嘧黄隆(sulfometuron-methyl)、乙黄黄隆(sulfosulfuron)、噻黄隆(thifensulfuron)、噻黄隆(thifensulfuron-methyl)、醚苯黄隆(triasulfuron)、苯黄隆(tribenuron)、苯黄隆(tribenuron-methyl)、三氟啶磺隆(trifloxysulfuron)、氟胺磺隆(triflusulfuron)、氟胺磺隆(triflusulfuron-methyl)和三氟甲磺隆(tritosulfuron),
咪唑啉酮类如咪草酯(imazamethabenz)、咪草酯(imazamethabenz-methyl)、咪草啶酸(imazamox)、甲基咪草烟(imazapic)、灭草烟(imazapyr)、灭草喹(imazaquin)和咪草烟(imazethapyr),
三唑并嘧啶类除草剂和磺酰苯胺类如唑嘧磺胺酸(cloransulam)、唑嘧磺胺盐(cloransulam-methyl)、唑嘧磺胺(diclosulam)、氟唑啶草(flumetsulam)、双氟磺草胺(florasulam)、唑草磺胺(metosulam)、五氟磺草胺(penoxsulam)、pyrimisulfan和啶磺草胺(pyroxsulam),
嘧啶基苯甲酸酯类如双嘧苯甲酸(bispyribac)、双嘧苯甲酸钠(bispyribac-sodium)、嘧苯草肟(pyribenzoxim)、环酯草醚(pyriftalid)、肟啶草(pyriminobac)、肟啶草(pyriminobac-methyl)、嘧硫苯甲酸(pyrithiobac)、嘧硫苯甲酸钠(pyrithiobac-sodium)、4-[[[2-[(4,6-二甲氧基-2-嘧啶基)氧基]苯基]甲基]氨基]苯甲酸1-甲基乙基酯(CAS 420138-41-6)、4-[[[2-[(4,6-二甲氧基-2-嘧啶基)氧基]苯基]甲基]氨基]苯甲酸丙基酯(CAS 420138-40-5)和N-(4-溴苯基)-2-[(4,6-二甲氧基-2-嘧啶基)氧基]苯甲胺(CAS420138-01-8),
磺酰氨基羰基三唑啉酮类除草剂如氟酮磺隆(flucarbazone)、氟酮磺隆钠(flucarbazone-sodium)、丙苯磺隆(propoxycarbazone)、丙苯磺隆(propoxycarbazone-sodium)、thiencarbazone和thiencarbazone-methyl,以及氟酮磺草胺(triafamone);
d2)PS II光合成抑制剂:
三唑啉酮类如胺唑草酮(amicarbazone),
三嗪类和甲硫基三嗪类如莠灭净(ametryn)、莠去津(atrazine)、氯代三嗪(chlorotriazine)、草净津(cyanazine)、敌草净(desmetryn)、戊草津(dimethametryn)、扑灭通(prometon)、扑草净(prometryne)、扑灭津(propazine)、西玛津(simazine)、西草净(simetryne)、甲氧去草净(terbumeton)、特丁津(terbuthylazine)、去草净(terbutryn)和草达津(trietazine),
三嗪酮类和三嗪二酮类如六嗪同(hexazinone)、苯嗪草(metamitron)和赛克津(metribuzin),
哒嗪酮类如杀草敏(chloridazone),
芳基脲类如氯溴隆(chlorobromuron)、绿麦隆(chlorotoluron)、枯草隆(chloroxuron)、丁隆(dimefuron)、敌草隆(diuron)、噻二唑隆(ethidimuron)、伏草隆(fluometuron)、非草隆(fenuron)、异丙隆(isoproturon)、异恶隆(isouron)、利谷隆(linuron)、噻唑隆(methabenzthiazuron)、色满隆(metobenzuron)、甲氧隆(metoxuron)、绿谷隆(monolinuron)、草不隆(neburon)、环草隆(siduron)、丁唑隆(tebuthiuron)和赛二唑素(thidiazuron),
苯基氨基甲酸酯类如异苯敌草(desmedipham)、卡草灵(karbutilat)、苯敌草(phenmedipham)和乙苯敌草(phenmedipham-ethyl),
腈类除草剂如杀草全(bromofenoxim)、溴苯腈(bromoxynil)及其盐和酯、碘苯腈(ioxynil)及其盐和酯,
尿嘧啶类如除草定(bromacil)、环草定(lenacil)和特草定(terbacil),
苯基哒嗪类如达草止(pyridate)和pyridafol,
酰胺类如蔬草灭(pentanochlor)和敌稗(propanil),以及
噻草平(bentazon)和噻草平(bentazon-sodium)。
d3)VLCFA抑制剂:
氯乙酰胺类如乙草胺(acetochlor)、甲草胺(alachlor)、丁草胺(butachlor)、克草胺(dimethachlor)、噻吩草胺(dimethanamid)、精噻吩草胺(dimethenamid-P)、吡草胺(metazachlor)、异丙甲草胺(metolachlor)、S-异丙甲草胺(metolachlor-S)、烯草胺(pethoxamid)、丙草胺(pretilachlor)、扑草胺(propachlor)、异丙草胺(propisochlor)和噻醚草胺(thenylchlor),
羟基乙酰苯胺类(oxyacetanilide)如氟噻草胺(flufenacet)和苯噻草胺(mefenacet),
乙酰胺类如草乃敌(diphenamid)、萘丙胺(naproanilide)和草萘胺(napropamide),
四唑啉酮类如四唑酰草胺(fentrazamide),
其他除草剂如莎稗磷(anilofos)、唑草胺(cafenstrole)、fenoxasulfone、ipfencarbazone、哌草磷(piperophos)、派罗克杀草砜(pyroxasulfone),以及
式VI.1、VI.2、VI.3、VI.4、VI.5、VI.6、VI.7、VI.8和VI.9的异唑啉化合物:
式VI的异唑啉化合物在本领域是已知的,例如由WO 2006/024820、WO 2006/037945、WO 2007/071900和WO 2007/096576已知;
在VLCFA抑制剂中优选氯乙酰胺类。
d4)有丝分裂抑制剂:
K1组化合物:
二硝基苯胺类如氟草胺(benfluralin)、地乐胺(butralin)、敌乐胺(dinitramine)、丁氟消草(ethalfluralin)、氟消草(fluchloralin)、黄草消(oryzalin)、胺硝草(pendimethalin)、氨基丙氟灵(prodiamine)和氟乐灵(trifluralin),
氨基磷酸酯类如胺草磷(amiprophos)、甲基胺草磷(amiprophos-methyl)和草胺磷(butamiphos),
苯甲酸类除草剂如敌草索(chlorthal)和敌草索(chlorthal-dimethyl),
吡啶类如氟硫草定(dithiopyr)和噻氟啶草(thiazopyr),
苯甲酰胺类如拿草特(propyzamide)和丙戊草胺(tebutam),
K2组化合物:氯苯胺灵(chlorpropham)、苯胺灵(propham)、长杀草(carbetamide)和甲氟燕灵(flamprop-m),
在这些中,优选K1组化合物,尤其是二硝基苯胺类;
优选的除草剂D选自:
d1)ALS抑制剂:
磺氨黄隆(amidosulfuron)、四唑黄隆(azimsulfuron)、苄嘧黄隆(bensulfuron-methyl)、双嘧苯甲酸钠(bispyribac-sodium)、氯嘧黄隆(chlorimuron-ethyl)、绿黄隆(chlorsulfuron)、唑嘧磺胺盐(cloransulam-methyl)、环丙黄隆(cyclosulfamuron)、唑嘧磺胺(diclosulam)、胺苯黄隆(ethametsulfuron-methyl)、乙氧嘧黄隆(ethoxysulfuron)、啶嘧黄隆(flazasulfuron)、双氟磺草胺(florasulam)、氟酮磺隆钠(flucarbazone-sodium)、氟吡磺隆(flucetosulfuron)、氟唑啶草(flumetsulam)、氟定黄隆(flupyrsulfuron-methyl-sodium)、甲酰氨磺隆(foramsulfuron)、吡氯黄隆(halosulfuron-methyl)、咪草酯(imazamethabenz-methyl)、咪草啶酸(imazamox)、甲基咪草烟(imazapic)、灭草烟(imazapyr)、灭草喹(imazaquin)、咪草烟(imazethapyr)、啶咪黄隆(imazosulfuron)、碘黄隆(iodosulfuron)、碘甲黄隆钠(iodosulfuron-methyl-sodium)、iofensulfuron、iofensulfuron-sodium、甲基二磺隆(mesosulfuron)、metazosulfuron、唑草磺胺(metosulam)、甲黄隆(metsulfuron-methyl)、烟嘧黄隆(nicosulfuron)、嘧苯胺磺隆(orthosulfamuron)、环丙氧黄隆(oxasulfuron)、五氟磺草胺(penoxsulam)、氟嘧黄隆(primisulfuron-methyl)、丙苯磺隆(propoxycarbazon-sodium)、propyrisulfuron、氟丙黄隆(prosulfuron)、吡嘧黄隆(pyrazosulfuron-ethyl)、嘧苯草肟(pyribenzoxim)、pyrimisulfan、环酯草醚(pyriftalid)、肟啶草(pyriminobac-methyl)、嘧硫苯甲酸钠(pyrithiobac-sodium)、啶磺草胺(pyroxsulam)、玉嘧黄隆(rimsulfuron)、嘧黄隆(sulfometuron-methyl)、乙黄黄隆(sulfosulfuron)、thiencarbazone-methyl、噻黄隆(thifensulfuron-methyl)、醚苯黄隆(triasulfuron)、苯黄隆(tribenuron-methyl)、三氟啶磺隆(trifloxysulfuron)、氟胺磺隆(triflusulfuron-methyl)、三氟甲磺隆(tritosulfuron)和氟酮磺草胺(triafamone);
d2)PS II光合成抑制剂:
莠灭净(ametryn)、胺唑草酮(amicarbazone)、莠去津(atrazine)、噻草平(bentazone)、噻草平(bentazone-sodium)、溴苯腈(bromoxynil)及其盐和酯、杀草敏(chloridazone)、绿麦隆(chlorotoluron)、草净津(cyanazine)、异苯敌草(desmedipham)、敌草隆(diuron)、伏草隆(fluometuron)、六嗪同(hexazinone)、碘苯腈(ioxynil)及其盐和酯、异丙隆(isoproturon)、环草定(lenacil)、利谷隆(linuron)、苯嗪草(metamitron)、噻唑隆(methabenzthiazuron)、赛克津(metribuzin)、苯敌草(phenmedipham)、敌稗(propanil)、达草止(pyridate)、西玛津(simazine)、去草净(terbutryn)、特丁津(terbuthylazine)和赛二唑素(thidiazuron);
d3)VLCFA抑制剂:
乙草胺(acetochlor)、甲草胺(alachlor)、莎稗磷(anilofos)、丁草胺(butachlor)、唑草胺(cafenstrole)、噻吩草胺(dimethanamid)、精噻吩草胺(dimethenamid-P)、四唑酰草胺(fentrazamide)、氟噻草胺(flufenacet)、苯噻草胺(mefenacet)、吡草胺(metazachlor)、异丙甲草胺(metolachlor)、S-异丙甲草胺(S-metolachlor)、萘丙胺(naproanilide)、草萘胺(napropamide)、丙草胺(pretilachlor)、fenoxasulfone、ipfencarbazone、派罗克杀草砜(pyroxasulfone)、噻醚草胺(thenylchlor)以及如上所述的VI.1、VI.2、VI.3、VI.4、VI.5、VI.6、VI.7、VI.8和VI.9的异唑啉化合物;
d4)有丝分裂抑制剂:
氟草胺(benfluralin)、氟硫草定(dithiopyr)、丁氟消草(ethalfluralin)、黄草消(oryzalin)、胺硝草(pendimethalin)、噻氟啶草(thiazopyr)和氟乐灵(trifluralin)。
特别优选的除草剂D选自:
d1)ALS抑制剂:苄嘧黄隆(bensulfuron-methyl)、双嘧苯甲酸钠(bispyribac-sodium)、环丙黄隆(cyclosulfamuron)、唑嘧磺胺(diclosulam)、氟唑啶草(flumetsulam)、氟定黄隆(flupyrsulfuron-methyl-sodium)、甲酰氨磺隆(foramsulfuron)、咪草啶酸(imazamox)、甲基咪草烟(imazapic)、灭草烟(imazapyr)、灭草喹(imazaquin)、咪草烟(imazethapyr)、啶咪黄隆(imazosulfuron)、碘黄隆(iodosulfuron)、碘甲黄隆钠(iodosulfuron-methyl-sodium)、iofensulfuron、iofensulfuron-sodium、甲基二磺隆(mesosulfuron)、metazosulfuron、烟嘧黄隆(nicosulfuron)、五氟磺草胺(penoxsulam)、丙苯磺隆(propoxycarbazon-sodium)、propyrisulfuron、吡嘧黄隆(pyrazosulfuron-ethyl)、嘧苯草肟(pyribenzoxim)、环酯草醚(pyriftalid)、啶磺草胺(pyroxsulam)、玉嘧黄隆(rimsulfuron)、乙黄黄隆(sulfosulfuron)、thiencarbazone-methyl、三氟甲磺隆(tritosulfuron)和氟酮磺草胺(triafamone);
d2)PS II光合成抑制剂:莠灭净(ametryn)、莠去津(atrazine)、噻草平(bentazone)、噻草平(bentazone-sodium)、溴苯腈(bromoxynil)及其盐和酯、敌草隆(diuron)、伏草隆(fluometuron)、六嗪同(hexazinone)、异丙隆(isoproturon)、利谷隆(linuron)、赛克津(metribuzin)、敌稗(propanil)、去草净(terbutryn)和特丁津(terbuthylazine);
d3)VLCFA抑制剂:乙草胺(acetochlor)、唑草胺(cafenstrole)、精噻吩草胺(dimethenamid-P)、四唑酰草胺(fentrazamide)、氟噻草胺(flufenacet)、苯噻草胺(mefenacet)、吡草胺(metazachlor)、异丙甲草胺(metolachlor)、S-异丙甲草胺(S-metolachlor)、fenoxasulfone、ipfencarbazone和派罗克杀草砜(pyroxasulfone);同样优选如上所述的VI.1、VI.2、VI.3、VI.4、VI.5、VI.6、VI.7、VI.8和VI.9的异唑啉化合物;
d4)有丝分裂抑制剂:胺硝草(pendimethalin)和氟乐灵(trifluralin)。
最优选的除草剂D列于下表3中:
表3
应理解的是任何具有羧基、氨基和/或羟基的除草剂D.1-D.20直接使用和/或以其可农用盐形式和/或以其可农用酯或酰胺形式使用。
优选如下本发明组合物,其中除草剂B选自b4)组,优选选自氟酮唑草(B.7)、氟嗪酮(B.8)、乳氟禾草灵(B.9)、炔丙唑草(B.10)、乙氧氟草醚(B.11)、苯嘧磺草胺(B.12)、磺胺草唑(B.13)和1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS 1258836-72-4)(B.14),尤其选自苯嘧磺草胺(B.12)和1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][[1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(CAS1258836-72-4)(B.14),并且除草剂D选自ALS抑制剂d1),优选选自灭草烟及其可农用盐(D14)、咪草烟及其可农用盐(D15)、嘧苯草肟(D16)和环酯草醚(D17);或者除草剂D选自PSII光合成抑制剂d2),优选选自莠去津(D.3)、敌草隆(D.4)、赛克津(D.5)、西玛津(D.6)、特丁津(D7)、噻草平及其可农用盐(D18)和溴苯腈及其可农用盐(D19),尤其选自莠去津(D.3)、西玛津(D.6)、特丁津(D7)、噻草平及其可农用盐(D18)和溴苯腈及其可农用盐(D19);或者除草剂D选自VLCFA抑制剂d3),优选派罗克杀草砜(D20)。
还优选如下本发明组合物,其包含选自b4)组化合物的第一除草剂B和选自如上所定义的d1)、d2)或d3)组化合物的除草剂D,该组合物进一步包含选自b6)组化合物,优选草甘膦及其可农用盐(B.26)或选自b7)组化合物,优选草铵膦及其可农用盐(B.27)的第二除草剂B。
进一步优选如下本发明组合物,其中除草剂B选自b5)组化合物,优选选自苯并双环酮(B.15)、bicyclopyrone(B.16)、异恶草酮(B.17)、吡氟草胺(B.18)、异氟草(B.19)、硝磺酮(B.20)、达草灭(B.21)、氟吡酰草胺(B.22)、磺草酮(B.23)、tembotrione(B.24)和topramezone(B.25),尤其选自苯并双环酮(B.15)、异氟草(B.19)、硝磺酮(B.20)和topramezone(B.25);并且除草剂D选自ALS抑制剂d1),优选选自灭草烟及其可农用盐(D14)、咪草烟及其可农用盐(D15)、嘧苯草肟(D16)和环酯草醚(D17);或者除草剂D选自PSII光合成抑制剂d2),优选选自莠去津(D.3)、敌草隆(D.4)、赛克津(D.5)、西玛津(D.6)、特丁津(D.7)、噻草平及其可农用盐(D18)和溴苯腈及其可农用盐(D19);或者除草剂D选自VLCFA抑制剂d3),优选选自乙草胺(D.8)、精噻吩草胺(D.9)、S-异丙甲草胺(D.10)、丙草胺(D.11)和派罗克杀草砜(D20)。
还优选如下本发明组合物,其包含选自b5)组化合物的第一除草剂B和选自如上所定义的d1)、d2)或d3)组化合物的除草剂D,该组合物进一步包含选自b6)组化合物,优选草甘膦及其可农用盐(B.26)或选自b7)组化合物,优选草铵膦及其可农用盐(B.27)的第二除草剂B。
进一步优选如下本发明组合物,其中除草剂B选自b6)组化合物,优选草甘膦及其可农用盐(B.26),并且除草剂D选自ALS抑制剂d1),优选选自烟嘧黄隆(D.1)、三氟甲磺隆(D.2)、双嘧苯甲酸钠(D13)、灭草烟(D14)、咪草烟(D15)、嘧苯草肟(D16)和环酯草醚(D17);或者除草剂D选自PS II光合成抑制剂d2),优选选自莠去津(D.3)、敌草隆(D4)、赛克津(D.5)、西玛津(D.6)、特丁津(D.7)、噻草平及其可农用盐(D18)和溴苯腈及其可农用盐(D19);或者除草剂D选自VLCFA抑制剂d3),优选选自乙草胺(D.8)、精噻吩草胺(D.9)、S-异丙甲草胺(D.10)、丙草胺(D.11)和派罗克杀草砜(D20);或者除草剂D选自d4)组化合物,优选胺硝草(D.12)。
进一步优选如下本发明组合物,其中除草剂B选自b7)组化合物,优选选自草铵膦及其可农用盐(B.27),并且除草剂D选自ALS抑制剂d1),优选选自烟嘧黄隆(D.1)、三氟甲磺隆(D.2)、双嘧苯甲酸钠(D13)、灭草烟及其可农用盐(D14)、咪草烟及其可农用盐(D15)、嘧苯草肟(D16)和环酯草醚(D17);或者除草剂D选自PS II光合成抑制剂d2),优选选自莠去津(D.3)、敌草隆(D4)、赛克津(D.5)、西玛津(D.6)、特丁津(D.7)、噻草平及其可农用盐(D18)和溴苯腈及其可农用盐(D19);或者除草剂D选自VLCFA抑制剂d3),优选选自乙草胺(D.8)、精噻吩草胺(D.9)、S-异丙甲草胺(D.10)、丙草胺(D.11)和派罗克杀草砜(D20);或者除草剂D选自d4)组化合物,优选胺硝草(D.12)。
进一步优选如下本发明组合物,其中除草剂B选自b13)组化合物,优选选自2,4-D及其可农用盐(B.31)及其可农用盐、麦草畏及其可农用盐(B.32)、氟草烟(B.33)、MCPA(B.34)、喹草酸及其可农用盐(B.35)和二氯喹啉酸及其可农用盐(B.36),尤其是2,4-D(B.31)及其可农用盐和麦草畏及其可农用盐(B.32),并且除草剂D选自ALS抑制剂d1),优选选自烟嘧黄隆(D.1)、三氟甲磺隆(D.2)、双嘧苯甲酸钠(D13)、灭草烟(D14)、咪草烟(D15)、嘧苯草肟(D16)或环酯草醚(D17);或者除草剂D选自VLCFA抑制剂d3),优选选自乙草胺(D.8)、精噻吩草胺(D.9)、S-异丙甲草胺(D.10)、丙草胺(D.11)和派罗克杀草砜(D20)。
还优选如下本发明组合物,其包含选自b13)组化合物的第一除草剂B和选自如上所定义的d1)或d3)组化合物的除草剂D,该组合物进一步包含选自b6)组化合物,优选选自草甘膦(B.26)及其可农用盐或选自b7)组化合物,优选选自草铵膦(B.27)及其可农用盐的第二除草剂B。
进一步优选如下本发明组合物,其中除草剂B选自b14)组化合物,优选二氟吡隆及其可农用盐(B.37),并且除草剂D选自ALS抑制剂d1),优选选自烟嘧黄隆(D.1)、三氟甲磺隆(D.2)、双嘧苯甲酸钠(D13)、灭草烟及其可农用盐(D14)、咪草烟及其可农用盐(D15)、嘧苯草肟(D16)或环酯草醚(D17);或者除草剂D选自VLCFA抑制剂d3),优选选自乙草胺(D.8)、精噻吩草胺(D.9)、S-异丙甲草胺(D.10)、丙草胺(D.11)和派罗克杀草砜(D20)。
还优选如下本发明组合物,其包含选自b14)组化合物的第一除草剂B和选自如上所定义的d1)或d3)组化合物的除草剂D,该组合物进一步包含选自b6)组化合物,优选选自草甘膦及其可农用盐(B.26)或选自b7)组化合物,优选草铵膦及其可农用盐(B.27)的第二除草剂B。
b1)-b15)组除草剂B、d1)-d4)组除草剂D和安全剂C是已知的除草剂和安全剂,例如见The Pesticide Manual,British Crop Protection Council,第16版,2012;TheCompendium of Pesticide Common Names(http://www.alanwood.net/pesticides/);Farm Chemicals Handbook 2000第86卷,Meister Publishing Company,2000;B.Hock,C.Fedtke,R.R.Schmidt,Herbizide[除草剂],Georg Thieme Verlag,Stuttgart 1995;W.H.Ahrens,Herbicide Handbook,第7版,Weed Science Society of America,1994;以及K.K.Hatzios,Herbicide Handbook,第7版增补,Weed Science Society of America,1998。2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷[CAS No.52836-31-4]也称为R-29148。4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷[CAS No.71526-07-3]也称为AD-67和MON 4660。
活性化合物的相应作用机理的归属基于现行知识。若一种活性化合物适用几种作用机理,则仅将该化合物归属于一种作用机理。
具有羧基的除草剂B和D及安全剂C可以以酸形式、如上所述的可农用盐形式或可农用衍生物形式用于本发明组合物中。
在麦草畏的情况下,合适的盐包括其中抗衡离子为可农用阳离子的那些。例如,麦草畏的合适盐是麦草畏钠(dicamba-sodium)、麦草畏钾(dicamba-potassium)、麦草畏甲铵盐(dicamba-methylammonium)、麦草畏二甲铵盐(dicamba-dimethylammonium)、麦草畏异丙铵盐(dicamba-isopropylammonium)、麦草畏二甘醇胺(dicamba-diglycolamine)、麦草畏乙醇胺(dicamba-olamine)、麦草畏二乙醇胺(dicamba-diolamine)、麦草畏三乙醇胺(dicamba-trolamine)、麦草畏-N,N-二(3-氨基丙基)甲胺和麦草畏-二亚乙基三胺。合适酯的实例是麦草畏甲酯(dicamba-methyl)和麦草畏丁氧基乙酯(dicamba-butotyl)。
2,4-D的合适盐是2,4-D铵盐(2,4-D-ammonium)、2,4-D二甲铵盐(2,4-D-dimethylammonium)、2,4-D二乙铵盐(2,4-D-diethylammonium)、2,4-D二乙醇铵盐(2,4-D-二乙醇胺)、2,4-D三乙醇铵盐、2,4-D异丙铵盐(2,4-D-isopropylammonium)、2,4-D三异丙醇铵盐(2,4-D-triisopropanolammonium)、2,4-D庚基铵盐(2,4-D-heptylammonium)、2,4-D十二烷基铵盐(2,4-D-dodecylammonium)、2,4-D十四烷基铵盐(2,4-D-tetradecylammonium)、2,4-D三乙基铵盐(2,4-D-triethylammonium)、2,4-D三(2-羟基丙基)铵盐、2,4-D三(异丙基)铵盐、2,4-D三乙醇胺(2,4-D-trolamine)、2,4-D锂、2,4-D钠。2,4-D的合适酯的实例是2,4-D丁氧基乙酯(2,4-D-butotyl)、2,4-D 2-丁氧基丙酯(2,4-D-2-butoxypropyl)、2,4-D 3-丁氧基丙酯(2,4-D-3-butoxypropyl)、2,4-D丁酯(2,4-D-butyl)、2,4-D乙酯(2,4-D-ethyl)、2,4-D乙基己基酯(2,4-D-ethylhexyl)、2,4-D异丁酯(2,4-D-isobutyl)、2,4-D异辛酯(2,4-D-isooctyl)、2,4-D异丙酯(2,4-D-isopropyl)、2,4-D甲基庚基酯(2,4-D-meptyl)、2,4-D甲酯(2,4-D-methyl)、2,4-D辛酯(2,4-D-octyl)、2,4-D戊酯(2,4-D-pentyl)、2,4-D丙酯(2,4-D-propyl)、2,4-D酯四氢糠基酯(2,4-D-tefuryl)和氯酰草膦(clacyfos)。
2,4-DB的合适盐例如为2,4-DB钠、2,4-DB钾和2,4-DB二甲铵盐。2,4-DB的合适酯例如为2,4-DB丁酯(2,4-DB-butyl)和2,4-DB异辛酯(2,4-DB-isoctyl)。
2,4-滴丙酸的合适盐例如为2,4-滴丙酸钾和2,4-滴丙酸二甲基铵盐。2,4-滴丙酸的合适酯的实例是2,4-滴丙酸丁氧基乙酯(dichlorprop-butotyl)和2,4-滴丙酸异辛酯(dichlorprop-isoctyl)。
MCPA的合适盐和酯包括MCPA丁氧基乙酯(MCPA-butotyl)、MCPA丁酯(MCPA-butyl)、MCPA二甲基铵盐、MCPA二乙醇胺、MCPA乙酯(MCPA-ethyl)、MCPA硫代乙酯(MCPA-thioethyl)、MCPA 2-乙基己基酯(MCPA-2-ethylhexyl)、MCPA异丁酯(MCPA-isobutyl)、MCPA异辛酯(MCPA-isoctyl)、MCPA异丙酯(MCPA-isopropyl)、MCPA异丙基铵盐、MCPA甲酯(MCPA-methyl)、MCPA乙醇胺、MCPA钾、MCPA钠和MCPA三乙醇胺。
MCPB的合适盐是MCPB钠。MCPB的合适酯是MCPB乙酯(MCPB-ethyl)。二氯皮考啉酸的合适盐是二氯皮考啉酸钾、二氯皮考啉酸乙醇胺和二氯皮考啉酸三(2-羟基丙基)铵盐。二氯皮考啉酸的合适酯的实例是二氯皮考啉酸甲酯(clopyralid-methyl)。
氟草烟的合适酯的实例是氟氯胺啶(fluroxypyr-meptyl)和氟草烟2-丁氧基-1-甲基乙基酯(fluroxypyr-2-butoxy-1-methylethyl),其中优选氟氯胺啶。
毒莠定的合适盐是毒莠定二甲铵盐、毒莠定钾、毒莠定三异丙醇铵盐、毒莠定三异丙基铵盐和毒莠定三乙醇胺。毒莠定的合适酯是毒莠定异辛酯(picloram-isoctyl)。
定草酯的合适盐是定草酯三乙铵盐。定草酯的合适酯例如是定草酯乙酯(triclopyr-ethyl)和定草酯丁氧基乙酯(triclopyr-butotyl)。
草灭平的合适盐和酯包括草灭平铵盐、草灭平二乙醇胺、草灭平甲酯(chloramben-methyl)、草灭平甲基铵盐和草灭平钠。2,3,6-TBA的合适盐和酯包括2,3,6-TBA二甲基铵盐、2,3,6-TBA锂、2,3,6-TBA钾和2,3,6-TBA钠。
氨草啶的合适盐和酯包括氨草啶钾和氨草啶三(2-羟基丙基)铵盐。
草甘膦的合适盐例如是草甘膦铵盐(glyphosate-ammonium)、草甘膦二铵盐(glyphosate-diammonium)、草甘膦二甲铵盐(glyphoste-dimethylammonium)、草甘膦异丙胺盐(glyphosate-isopropylammonium)、草甘膦钾、草甘膦钠、草硫膦(glyphosate-trimesium)以及乙醇胺和二乙醇胺盐,优选草甘膦铵盐、草甘膦异丙胺盐和草硫膦(sulfosate)。
草铵膦的合适盐例如是草铵膦(glufosinate-ammonium)。
草铵膦(glufosinate-P)的合适盐例如是草铵膦(glufosinate-P-ammonium)。
溴苯腈的合适盐和酯例如是溴苯腈丁酸酯、溴苯腈庚酸酯、溴苯腈辛酸酯、溴苯腈钾和溴苯腈钠。
碘苯腈的合适盐和酯例如是碘苯腈辛酸酯、碘苯腈钾和碘苯腈钠。
2甲4氯丙酸的合适盐和酯包括2甲4氯丙酸丁氧基乙酯(mecoprop-butotyl)、2甲4氯丙酸二甲基铵盐、2甲4氯丙酸二乙醇胺、mecoprop-ethadyl、2甲4氯丙酸2-乙基己基酯(mecoprop-2-ethylhexyl)、2甲4氯丙酸异辛酯(mecoprop-isoctyl)、2甲4氯丙酸甲酯(mecoprop-methyl)、2甲4氯丙酸钾、2甲4氯丙酸钠和2甲4氯丙酸三乙醇胺。
高2甲4氯丙酸的合适盐例如为高2甲4氯丙酸丁氧基乙酯(mecoprop-P-butotyl)、高2甲4氯丙酸二甲基铵盐、高2甲4氯丙酸2-乙基己基酯(mecoprop-P-2-ethylhexyl)、高2甲4氯丙酸异丁酯(mecoprop-P-isobutyl)、高2甲4氯丙酸钾和高2甲4氯丙酸钠。
二氟吡隆的合适盐例如是二氟吡隆钠。
抑草生的合适盐例如是抑草生钠。
aminocyclopyrachlor的合适盐和酯例如是aminocyclopyrachlor二甲基铵盐、aminocyclopyrachlor甲酯、aminocyclopyrachlor三异丙醇铵盐、aminocyclopyrachlor钠和aminocyclopyrachlor钾。
二氯喹啉酸的合适盐例如是二氯喹啉酸二甲基铵盐。
喹草酸的合适盐例如是喹草酸二甲基铵盐。
咪草啶酸的合适盐例如是咪草啶酸铵盐。
甲基咪草烟的合适盐例如是甲基咪草烟铵盐和甲基咪草烟异丙基铵盐。
灭草烟的合适盐例如是灭草烟铵盐和灭草烟异丙基铵盐。
灭草喹的合适盐例如是灭草喹铵盐。
咪草烟的合适盐例如是咪草烟铵盐和咪草烟异丙基铵盐。
topramezone的合适盐例如是topramezone钠。
这里和下文中,术语“二元组合物”包括包含一种或多种,例如1、2或3种除草剂A和一种或多种,例如1、2或3种除草剂B的组合物。相应地,术语“三元组合物”包括包含一种或多种,例如1、2或3种除草剂A,例如1、2或3,除草剂B和至少一种除草剂D的组合物。
进一步优选的实施方案涉及对应于上述二元和三元组合物且额外包含安全剂C,尤其选自解草酮(C.1)、喹氧乙酸(C.2)、cyprosulfamide(C.3)、抑害胺(C.4)、解草唑(C.5)、解草啶(C.6)、解草呋(C.7)、双苯唑酸(C.8)、吡咯二酸(C.9)、4-二氯乙酰基-1-氧杂-4-氮杂螺[4.5]癸烷(MON4660,CAS 71526-07-3)(C.10)和2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷(R-29148,CAS 52836-31-4)(C.11)的安全剂C的组合物。
在包含至少一种除草剂A和至少一种除草剂B的二元组合物中,A:B的重量比通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。
在同时包含至少一种除草剂A、至少一种除草剂B和至少一种安全剂C的组合物中,重量比A:B通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1;重量比A:C通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1;并且重量比B:C通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。重量比(A+B):C优选为1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。
在包含至少一种除草剂A、至少一种除草剂B和除草剂D的三元组合物中,重量比A:B、A:D和B:D在每种情况下通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。重量比(A+B):D优选为1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。
在包含至少一种除草剂A、至少一种除草剂B、除草剂D和至少一种安全剂C的组合物中,重量比A:B、A:C、A:D、B:C、B:D和C:D在每种情况下通常为1:1000-1000:1,优选1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。重量比(A+B):C和(A+B):D在每种情况下优选为1:500-500:1,尤其是1:250-250:1,特别优选1:75-75:1。重量比(A+B+D):C优选为1:250-250:1,特别优选1:75-75:1。
特别优选表A0-K11中所列下列本发明组合物:
表A0
表A1.组合物a1.1.c1-a1.1550.c1,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含解草酮C.1。
表A2.组合物a1.1.c2-a1.1550.c2,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含喹氧乙酸C.2。
表A3.组合物a1.1.c3-a1.1550.c3,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含cyprosulfamideC.3。
表A4.组合物a1.1.c4-a1.1550.c4,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含抑害胺C.4。
表A5.组合物a1.1.c5-a1.1550.c5,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含解草啶C.5。
表A6.组合物a1.1.c6-a1.1550.c6,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含解草唑C.6。
表A7.组合物a1.1.c7-a1.1550.c7,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含解草呋C.7。
表A8.组合物a1.1.c8-a1.1550.c8,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含双苯唑酸C.8。
表A9.组合物a1.1.c9-a1.1550.c9,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含吡咯二酸C.9。
表A10.组合物a1.1.c10-a1.1550.c10,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含4-二氯乙酰基-1-氧杂-4-氮杂螺-[4.5]癸烷C.10。
表A11.组合物a1.1.c11-a1.1550.c11,其与表A0的相应组合物a1.1-a1.1550的不同仅在于它们各自额外包含2,2,5-三甲基-3-二氯乙酰基-1,3-唑烷C.11。
表B0.组合物a2.1-a2.1550,其与表A0的相应组合物1a.1-1a.1550的不同仅在于在每种情况下组分a1)被a2)替代。
表B1.组合物a2.1.c1-a2.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a2)替代。
表B2.组合物a2.1.c2-a2.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a2)替代。
表B3.组合物a2.1.c3-a2.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a2)替代。
表B4.组合物a2.1.c4-a2.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a2)替代。
表B5.组合物a2.1.c5-a2.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a2)替代。
表B6.组合物a2.1.c6-a2.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a2)替代。
表B7.组合物a2.1.c7-a2.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a2)替代。
表B8.组合物a2.1.c8-a2.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a2)替代。
表B9.组合物a2.1.c9-a2.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a2)替代。
表B10.组合物a2.1.c10-a2.1550.c10,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a2)替代。
表B11.组合物a2.1.c11-a2.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a2)替代。
表C0.组合物a3.1-a3.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a3)替代。
表C1.组合物a3.1.c1-a3.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a3)替代。
表C2.组合物a3.1.c2-a3.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a3)替代。
表C3.组合物a3.1.c3-a3.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a3)替代。
表C4.组合物a3.1.c4-a3.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a3)替代。
表C5.组合物a3.1.c5-a3.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a3)替代。
表C6.组合物a3.1.c6-a3.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a3)替代。
表C7.组合物a3.1.c7-a3.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a3)替代。
表C8.组合物a3.1.c8-a3.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a3)替代。
表C9.组合物a3.1.c9-a3.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a3)替代。
表C10.组合物a3.1.c10-a3.1550.c10,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a3)替代。
表C11.组合物a3.1.c11-a3.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a3)替代。
表D0.组合物a4.1-a4.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a4)替代。
表D1.组合物a4.1.c1-a4.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a4)替代。
表D2.组合物a4.1.c2-a4.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a4)替代。
表D3.组合物a4.1.c3-a4.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a4)替代。
表D4.组合物a4.1.c4-a4.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a4)替代。
表D5.组合物a4.1.c5-a4.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a4)替代。
表D6.组合物a4.1.c6-a4.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a4)替代。
表D7.组合物a4.1.c7-a4.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a4)替代。
表D8.组合物a4.1.c8-a4.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a4)替代。
表D9.组合物a4.1.c9-a4.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a4)替代。
表D10.组合物a4.1.c10-a4.1550.c10,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a4)替代。
表D11.组合物a4.1.c11-a4.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a4)替代。
表E0.组合物a5.1-a5.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a5)替代。
表E1.组合物a5.1.c1-a5.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a5)替代。
表E2.组合物a5.1.c2-a5.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a5)替代。
表E3.组合物a5.1.c3-a5.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a5)替代。
表E4.组合物a5.1.c4-a5.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a5)替代。
表E5.组合物a5.1.c5-a5.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a5)替代。
表E6.组合物a5.1.c6-a5.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a5)替代。
表E7.组合物a5.1.c7-a5.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a5)替代。
表E8.组合物a5.1.c8-a5.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a5)替代。
表E9.组合物a5.1.c9-a5.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a5)替代。
表E10.组合物a5.1.c10-a5.1550.c10,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a5)替代。
表E11.组合物a5.1.c11-a5.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a5)替代。
表F0.组合物a6.1-a6.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a6)替代。
表F1.组合物a6.1.c1-a6.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a6)替代。
表F2.组合物a6.1.c2-a6.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a6)替代。
表F3.组合物a6.1.c3-a6.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a6)替代。
表F4.组合物a6.1.c4-a6.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a6)替代。
表F5.组合物a6.1.c5-a6.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a6)替代。
表F6.组合物a6.1.c6-a6.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a6)替代。
表F7.组合物a6.1.c7-a6.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a6)替代。
表F8.组合物a6.1.c8-a6.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a6)替代。
表F9.组合物a6.1.c9-a6.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a6)替代。
表F10.组合物a6.1.c10-a6.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a6)替代。
表F11.组合物a6.1.c11-a6.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a6)替代。
表G0.组合物a7.1-a7.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a7)替代。
表G1.组合物a7.1.c1-a7.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a7)替代。
表G2.组合物a7.1.c2-a7.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a7)替代。
表G3.组合物a7.1.c3-a7.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a7)替代。
表G4.组合物a7.1.c4-a7.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a7)替代。
表G5.组合物a7.1.c5-a7.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a7)替代。
表G6.组合物a7.1.c6-a7.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a7)替代。
表G7.组合物a7.1.c7-a7.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a7)替代。
表G8.组合物a7.1.c8-a7.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a7)替代。
表G9.组合物a7.1.c9-a7.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a7)替代。
表G10.组合物a7.1.c10-a7.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a7)替代。
表G11.组合物a7.1.c11-a7.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a7)替代。
表H0.组合物a8.1-a8.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a8)替代。
表H1.组合物a8.1.c1-a8.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a8)替代。
表H2.组合物a8.1.c2-a8.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a8)替代。
表H3.组合物a8.1.c3-a8.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a8)替代。
表H4.组合物a8.1.c4-a8.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a8)替代。
表H5.组合物a8.1.c5-a8.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a8)替代。
表H6.组合物a8.1.c6-a8.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a8)替代。
表H7.组合物a8.1.c7-a8.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a8)替代。
表H8.组合物a8.1.c8-a8.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a8)替代。
表H9.组合物a8.1.c9-a8.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a8)替代。
表H10.组合物a8.1.c10-a8.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a8)替代。
表H11.组合物a8.1.c11-a8.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a8)替代。
表I0.组合物a9.1-a9.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a9)替代。
表I1.组合物a9.1.c1-a9.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a9)替代。
表I2.组合物a9.1.c2-a9.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a9)替代。
表I3.组合物a9.1.c3-a9.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a9)替代。
表I4.组合物a9.1.c4-a9.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a9)替代。
表I5.组合物a9.1.c5-a9.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a9)替代。
表I6.组合物a9.1.c6-a9.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a9)替代。
表I7.组合物a9.1.c7-a9.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a9)替代。
表I8.组合物a9.1.c8-a9.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a9)替代。
表I9.组合物a9.1.c9-a9.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a9)替代。
表I10.组合物a9.1.c10-a9.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a9)替代。
表I11.组合物a9.1.c11-a9.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a9)替代。
表J0.组合物a10.1-a10.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a10)替代。
表J1.组合物a10.1.c1-a10.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a10)替代。
表J2.组合物a10.1.c2-a10.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a10)替代。
表J3.组合物a10.1.c3-a10.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a10)替代。
表J4.组合物a10.1.c4-a10.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a10)替代。
表J5.组合物a10.1.c5-a10.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a10)替代。
表J6.组合物a10.1.c6-a10.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a10)替代。
表J7.组合物a10.1.c7-a10.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a10)替代。
表J8.组合物a10.1.c8-a10.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a10)替代。
表J9.组合物a10.1.c9-a10.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a10)替代。
表J10.组合物a10.1.c10-a10.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a10)替代。
表J11.组合物a10.1.c11-a10.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a10)替代。
表K0.组合物a11.1-a11.1550,其与表A0的相应组合物a1.1-a1.1550的不同仅在于在每种情况下组分a1)被a11)替代。
表K1.组合物a11.1.c1-a11.1550.c1,其与表A1的相应组合物a1.1.c1-a1.1550.c1的不同仅在于在每种情况下组分a1)被a11)替代。
表K2.组合物a11.1.c2-a11.1550.c2,其与表A2的相应组合物a1.1.c2-a1.1550.c2的不同仅在于在每种情况下组分a1)被a11)替代。
表K3.组合物a11.1.c3-a11.1550.c3,其与表A3的相应组合物a1.1.c3-a1.1550.c3的不同仅在于在每种情况下组分a1)被a11)替代。
表K4.组合物a11.1.c4-a11.1550.c4,其与表A4的相应组合物a1.1.c4-a1.1550.c4的不同仅在于在每种情况下组分a1)被a11)替代。
表K5.组合物a11.1.c5-a11.1550.c5,其与表A5的相应组合物a1.1.c5-a1.1550.c5的不同仅在于在每种情况下组分a1)被a11)替代。
表K6.组合物a11.1.c6-a11.1550.c6,其与表A6的相应组合物a1.1.c6-a1.1550.c6的不同仅在于在每种情况下组分a1)被a11)替代。
表K7.组合物a11.1.c7-a11.1550.c7,其与表A7的相应组合物a1.1.c7-a1.1550.c7的不同仅在于在每种情况下组分a1)被a11)替代。
表K8.组合物a11.1.c8-a11.1550.c8,其与表A8的相应组合物a1.1.c8-a1.1550.c8的不同仅在于在每种情况下组分a1)被a11)替代。
表K9.组合物a11.1.c9-a11.1550.c9,其与表A9的相应组合物a1.1.c9-a1.1550.c9的不同仅在于在每种情况下组分a1)被a11)替代。
表K10.组合物a11.1.c10-a11.1550.c,其与表A10的相应组合物a1.1.c10-a1.1550.c10的不同仅在于在每种情况下组分a1)被a11)替代。
表K11.组合物a11.1.c11-a11.1550.c11,其与表A11的相应组合物a1.1.c11-a1.1550.c11的不同仅在于在每种情况下组分a1)被a11)替代。
本发明还涉及包含助剂和至少一种本发明组合物的农业化学组合物。
农业化学组合物包含农药有效量的至少一种本发明组合物。术语“有效量”表示足以防治不希望的植物,尤其是在栽培植物中防治不希望的植物且不会对被处理植物产生显著损害的活性成分量。该量可以在宽范围内变化且取决于各种因素,如待防治植物、被处理栽培植物或材料、气候条件和所用具体本发明组合物。
可以将化合物A和B及任选C和D、其盐或衍生物转化成常规类型的农业化学组合物,例如溶液、乳液、悬浮液、粉剂、粉末、糊、颗粒、模压品、胶囊及其混合物。农业化学组合物类型的实例是悬浮液(例如SC、OD、FS),可乳化浓缩物(例如EC),乳液(例如EW、EO、ES、ME),胶囊(例如CS、ZC),糊,锭剂,可湿性粉末或粉剂(例如WP、SP、WS、DP、DS),模压品(例如BR、TB、DT),颗粒(例如WG、SG、GR、FG、GG、MG),杀虫制品(例如LN)以及处理植物繁殖材料如种子的凝胶配制剂(例如GF)。这些和其他农业化学组合物类型在“Catalogue ofpesticide formulation types and international coding system”,TechnicalMonograph,第2期,2008年5月第6版,CropLife International中有定义。
农业化学组合物如Mollet和Grubemann,Formulation technology,Wiley VCH,Weinheim,2001;或Knowles,New developments in crop protection productformulation,Agrow Reports DS243,T&F Informa,London,2005所述以已知方式制备。
合适的助剂是溶剂,液体载体,固体载体或填料,表面活性剂,分散剂,乳化剂,润湿剂,辅助剂,加溶剂,渗透促进剂,保护性胶体,粘附剂,增稠剂,保湿剂,驱除剂,引诱剂,进食刺激剂,相容剂,杀菌剂,防冻剂,消泡剂,着色剂,增粘剂和粘合剂。
合适的溶剂和液体载体是水和有机溶剂;植物或动物来源的油;脂族、环状和芳族烃类;醇类;二醇类;DMSO;酮类;酯类;脂肪酸;膦酸酯;胺类;酰胺类;以及它们的混合物。
合适的固体载体或填料是矿土;多糖;肥料;植物来源的产品,以及它们的混合物。
合适的表面活性剂是表面活性化合物,如阴离子、阳离子、非离子和两性表面活性剂,嵌段聚合物,聚电解质,以及它们的混合物。该类表面活性剂可以用作乳化剂、分散剂、加溶剂、润湿剂、渗透促进剂、保护性胶体或辅助剂。表面活性剂的实例列于McCutcheon’s,第1卷:Emulsifiers & Detergents,McCutcheon’s Directories,Glen Rock,USA,2008(International Ed.或North American Ed.)中。
合适的辅助剂是本身具有可忽略的农药活性或者本身甚至没有农药活性且改善化合物I对目标物的生物学性能的化合物。实例是表面活性剂,矿物油或植物油以及其他助剂。其他实例由Knowles,Adjuvants and additives,Agrow Reports DS256,T&F InformaUK,2006,第5章列出。
合适的增稠剂是多糖、无机粘土、聚羧酸盐和硅酸盐。
合适的杀菌剂是拌棉醇(bronopol)和异噻唑啉酮衍生物如烷基异噻唑啉酮和苯并异噻唑啉酮。
合适的防冻剂是乙二醇、丙二醇、尿素和甘油。
合适的消泡剂是聚硅氧烷、长链醇和脂肪酸盐。
合适的着色剂(例如着红色、蓝色或绿色)是低水溶性颜料和水溶性染料。实例是无机着色剂(例如氧化铁、氧化钛、六氰合铁酸铁)和有机着色剂(例如茜素着色剂、偶氮着色剂和酞菁着色剂)。
合适的增粘剂或粘合剂是聚乙烯吡咯烷酮、聚乙酸乙烯酯、聚乙烯醇、聚丙烯酸酯、生物蜡或合成蜡以及纤维素醚。
为了处理植物繁殖材料,尤其是种子,通常使用种子处理用溶液(LS),悬浮乳液(SE),可流动浓缩物(FS),干处理用粉末(DS),淤浆处理用水分散性粉末(WS),水溶性粉末(SS),乳液(ES),可乳化浓缩物(EC)和凝胶(GF)。
组合物分别在植物繁殖材料,尤其是种子上的施用方法包括繁殖材料的拌种、包衣、造粒、撒粉、浸泡和犁沟内施用方法。优选通过不诱发萌发的方法,例如通过拌种、造粒、包衣和撒粉将组合物分别施用于植物繁殖材料上。
可以向活性成分或包含它们的组合物中作为预混物加入或者合适的话在紧临使用前加入(桶混合)各种类型的油、润湿剂、辅助剂、肥料或微营养素和其他农药(例如杀虫剂、杀真菌剂、生长调节剂、安全剂)。这些试剂可以以1:100-100:1的重量比与本发明组合物混合。
用户通常将本发明农业化学组合物用于前剂量装置、小背包喷雾器、喷雾罐、喷雾飞机或灌溉系统。通常将该农业化学组合物用水、缓冲剂和/或其他助剂配制至所需施用浓度,从而得到即用喷雾液或本发明农业化学组合物。每公顷农业利用区通常施用20-2000升即用喷雾液。
根据一个实施方案,用户可以在喷雾罐中混合本发明农业化学组合物的各组分或部分预混的组分,例如包含除草剂A和选自B组和任选C和/或D组的活性化合物的农业化学组分并且合适的话可以加入其他助剂和添加剂。
在另一实施方案中,用户可以自己在喷雾罐中混合本发明农业化学组合物的各组分,例如成套包装的各部分或二元或三元混合物的各部分并且合适的话可以加入其他助剂。
在另一实施方案中,可以联合(例如在桶混合之后)或依次施用本发明农业化学组合物的各组分或部分预混的组分,例如包含除草剂A和选自B组和任选C和/或D组的活性化合物的组分。
因此,本发明的一个实施方案涉及单组分农业化学组合物,其包含至少一种除草剂A和至少一种选自除草剂B的其他活性化合物以及任选安全剂C和任选除草剂D,以及固体或液体载体和合适的话一种或多种表面活性剂。
因此,本发明的另一实施方案涉及双组分农业化学组合物,其包含含有至少一种除草剂A、固体或液体载体和合适的话一种或多种表面活性剂的第一组分以及含有至少一种除草剂B、任选安全剂C和/或除草剂D、固体或液体载体和合适的话一种或多种表面活性剂的第二组分。
除草剂A和至少一种其他活性化合物B和/或C可以在植物出苗之前、之中或之后联合或分开、同时或依次配制和施用。在分开施用的情况下,活性化合物A、B、C和D的施用顺序不太重要。唯一重要的是至少一种活性化合物A以及至少一种其他活性化合物B和任选C和/或D同时存在于作用位置,即同时与待防治植物接触或被其吸收。
本发明组合物非常有效地防治非作物区域的植物生长,尤其是在高施用率下。它们在作物如小麦、稻、玉米、大豆和棉花中作用于阔叶杂草和禾本科杂草而不对农作物引起任何显著的损害。该效果主要在低施用率下观察到。。
本发明组合物主要通过喷雾叶子而施用于植物上。这里可以使用例如水作为载体通过常规喷雾技术使用约50-1000l/ha(例如300-400l/ha)的喷雾液量进行施用。该除草组合物还可以通过低体积或超低体积方法或以微颗粒形式施用。
本发明除草组合物的施用可以在不希望的植物出苗之前、之中和/或之后,优选之中和/或之后进行。
本发明除草组合物可以出苗前或出苗后施用,或者与农作物的种子一起施用。还可以通过施用用本发明组合物预处理的农作物的种子而施用化合物和组合物。若活性化合物A和B以及合适的话C不能被某些农作物良好地耐受,则可以使用其中借助喷雾设备喷雾除草组合物以使它们尽可能不接触敏感农作物的叶子,而使活性化合物到达生长在下面的不希望的植物的叶子或裸露的土壤表面的施用技术(后引导,最后耕作程序)。
在另一实施方案中,可以通过处理种子而施用本发明组合物。种子的处理基本包括所有本领域熟练技术人员熟知的基于本发明式I化合物或由其制备的组合物的程序(拌种、种子包衣、种子撒粉、种子浸泡、种子包膜、种子多层包衣、种子包壳、种子浸滴和种子造粒)。此时可以加以稀释或不加稀释地施用除草组合物。
术语“种子”包括所有类型的种子,如玉米、种子、果实、块茎、秧苗和类似形式。这里优选术语种子描述的是玉米和种子。所用种子可以是上述有用植物的种子,但还可以是转基因植物或通过常规育种方法得到的植物的种子。
此外,可能有利的是单独或与其他作物保护剂组合联合施用本发明组合物,例如与用于防治害虫或植物病原性真菌或细菌的试剂联合或与调节生长的活性化合物联合。还令人感兴趣的是与无机盐溶液的溶混性,所述溶液用于处理营养和痕量元素缺乏。还可以加入非植物毒性油和油浓缩物。
当用于植物保护中时,没有配制助剂的活性化合物,即除草剂A和B以及合适的话除草剂D和安全剂C的施用量取决于所需效果的种类为0.001-2kg/ha,优选0.005-2kg/ha,更优选0.05-0.9kg/ha,尤其是0.1-0.75kg/ha。
在本发明的另一实施方案中,除草剂A和B以及合适的话除草剂D和安全剂C的施用率为0.001-3kg/ha,优选0.005-2.5kg/ha,尤其是0.01-2kg/ha活性成分(a.i.)。
在本发明的另一优选实施方案中,除草剂A的施用率取决于防治目标、季节、目标植物和生长阶段为0.1-3000g/ha,优选10-1000g/ha。
在本发明的另一优选实施方案中,除草剂A的施用率为0.1-5000g/ha,优选1-2500g/ha或5-2000g/ha。
在本发明的另一优选实施方案中,除草剂A的施用率为0.1-1000g/ha,优选1-750g/ha,更优选5-500g/ha。
所要求的除草剂化合物B和任选D的施用率通常为0.0005-2.5kg/ha,优选0.005-2kg/ha或0.01-1.5kg/h a.i.。
所要求的安全剂C的施用率通常为0.0005-2.5kg/ha,优选0.005-2kg/ha或0.01-1.5kg/h a.i.。
在植物繁殖材料如种子例如通过撒粉、包衣或浸透种子的处理中,每100kg植物繁殖材料(优选种子)通常要求活性化合物的量为0.1-1000g,优选1-1000g,更优选1-100g,最优选5-100g。
在本发明的另一实施方案中,为了处理种子,活性化合物,即除草剂A和B以及合适的话安全剂C和/或除草剂D的施用量通常以0.001-10kg/100kg种子的量使用。
当用于保护材料或储存产品中时,活性化合物的施用量取决于施用区域的种类和所需效果。在材料保护中常用的施用量为0.001g-2kg,优选0.005g-1kg活性化合物/立方米被处理材料。
在本发明方法中,除草剂A、其他除草剂B以及任选安全剂C和除草剂D是否联合或分开配制和施用并不重要。
在分开施用的情况下,施用以何种顺序进行不太重要。仅仅必要的是除草剂A和除草剂B、任选除草剂D以及任选安全剂C在允许活性成分同时作用于植物上的时间范围内,优选在至多14天,尤其是至多7天的时间范围内施用。
取决于所述施用方法,本发明组合物可以额外用于许多其他农作物以消除不希望的植物。合适的作物实例如下:洋葱(Allium cepa)、凤梨(Ananas comosus)、落花生(Arachis hypogaea)、石刁柏(Asparagus officinalis)、燕麦(Avena sativa)、甜菜(Betavulgaris spec.altissima)、甜菜(Beta vulgaris spec.rapa)、欧洲油菜(Brassicanapus var.napus)、芜青甘蓝(Brassica napus var.napobrassica)、芜青(Brassica rapavar.silvestris)、羽衣甘蓝(Brassica oleracea)、黑芥(Brassica nigra)、大叶茶(Camellia sinensis)、红花(Carthamus tinctorius)、美国山核桃(Caryaillinoinensis)、柠檬(Citrus limon)、甜橙(Citrus sinensis)、小果咖啡(Coffeaarabica)(中果咖啡(Coffea canephora)、大果咖啡(Coffea liberica))、黄瓜(Cucumissativus)、狗牙根(Cynodon dactylon)、胡萝卜(Daucus carota)、油棕(Elaeisguineensis)、欧洲草莓(Fragaria vesca)、大豆(Glycine max)、陆地棉(Gossypiumhirsutum)(树棉(Gossypium arboreum)、草棉(Gossypium herbaceum)、Gossypiumvitifolium)、向日葵(Helianthus annuus)、Hevea brasiliensis、大麦(Hordeumvulgare)、啤酒花(Humulus lupulus)、甘薯(Ipomoea batatas)、核桃(Juglans regia)、兵豆(Lens culinaris)、亚麻(Linum usitatissimum)、番茄(Lycopersicon lycopersicum)、苹果属(Malus spec.)、木薯(Manihot esculenta)、紫苜蓿(Medicago sativa)、芭蕉属(Musa spec.)、烟草(Nicotiana tabacum)(黄花烟草(N.rustica))、油橄榄(Oleaeuropaea)、稻(Oryza sativa)、金甲豆(Phaseolus lunatus)、菜豆(Phaseolusvulgaris)、欧洲云杉(Picea abies)、松属(Pinus spec.)、开心果(Pistacia vera)、Pisumsativum、欧洲甜樱桃(Prunus avium)、Prunus persica、西洋梨(Pyrus communis)、杏(Prunus armeniaca)、欧洲酸樱桃(Prunus cerasus)、扁桃(Prunus dulcis)和欧洲李(Prunus domestica)、Ribes sylvestre、蓖麻(Ricinus communis)、甘蔗(Saccharumofficinarum)、黑麦(Secale cereale)、白芥(Sinapis alba)、马铃薯(Solanumtuberosum)、两色蜀黍(Sorghum bicolor)(高粱(S.vulgare))、可可树(Theobromacacao)、红车轴草(Trifolium pratense)、普通小麦(Triticum aestivum)、小黑麦(Triticale)、硬粒小麦(Triticum durum)、蚕豆(Vicia faba)、葡萄(Vitis vinifera)、玉蜀黍(Zea mays)。
优选的作物是落花生(Arachis hypogaea)、甜菜(Beta vulgarisspec.altissima)、欧洲油菜(Brassica napus var.napus)、羽衣甘蓝(Brassicaoleracea)、柠檬(Citrus limon)、甜橙(Citrus sinensis)、小果咖啡(Coffea arabica)(中果咖啡(Coffea canephora)、大果咖啡(Coffea liberica))、狗牙根(Cynodondactylon)、大豆(Glycine max)、陆地棉(Gossypium hirsutum)(树棉(Gossypiumarboreum)、草棉(Gossypium herbaceum)、Gossypium vitifolium)、向日葵(Helianthusannuus)、大麦(Hordeum vulgare)、核桃(Juglans regia)、兵豆(Lens culinaris)、亚麻(Linum usitatissimum)、番茄(Lycopersicon lycopersicum)、苹果属(Malus spec.)、紫苜蓿(Medicago sativa)、烟草(Nicotiana tabacum)(黄花烟草(N.rustica))、油橄榄(Olea europaea)、稻(Oryza sativa)、金甲豆(Phaseolus lunatus)、菜豆(Phaseolusvulgaris)、开心果(Pistacia vera)、Pisum sativum、扁桃(Prunus dulcis)、甘蔗(Saccharum officinarum)、黑麦(Secale cereale)、马铃薯(Solanum tuberosum)、两色蜀黍(Sorghum bicolor)(高粱(S.vulgare))、小黑麦(Triticale)、普通小麦(Triticumaestivum)、硬粒小麦(Triticum durum)、蚕豆(Vicia faba)、葡萄(Vitis vinifera)和玉蜀黍(Zea mays)。
尤其优选的作物是禾谷类作物、玉米、大豆、稻、油籽油菜、棉花、土豆、花生或多年生作物。
本发明组合物还可以用于基因修饰植物中。术语“基因修饰植物”应理解为其基因材料通过使用重组DNA技术修饰而包括对所述植物品种的基因组而言非天生的DNA的插入序列或呈现对所述品种的基因组而言天生的DNA的删减,其中修饰不易单独通过杂交、突变或自然重组得到。特殊的基因修饰植物通常是通过自然育种或繁殖方法由其基因组为通过利用重组DNA技术直接处理的基因组的传代植物遗传获得其基因修饰的植物。通常将一个或多个基因整合到基因修饰植物的基因材料中以改善植物的某些性能。这类基因修饰还包括但不限于蛋白质、寡肽或多肽的靶向翻译后修饰,例如通过在其中引入允许、降低或促进糖基化或聚合物加成如异戊二烯化、乙酰化或法呢基化或PEG结构部分连接的氨基酸突变。
通过育种、诱变或基因工程修饰的植物例如因常规育种或基因工程方法而耐受特殊类别除草剂的施用,这些除草剂如植物生长素除草剂如麦草畏(dicamba)或2,4-D;漂白剂除草剂如4-羟基苯基丙酮酸二加氧酶(HPPD)抑制剂或八氢番茄红素去饱和酶(PDS)抑制剂;乙酰乳酸合成酶(ALS)抑制剂,例如磺酰脲类或咪唑啉酮类;烯醇丙酮酰莽草酸3-磷酸合成酶(EPSPS)抑制剂,例如草甘膦(glyphosate);谷氨酰胺合成酶(GS)抑制剂,例如草铵膦(glufosinate);原卟啉原-IX氧化酶抑制剂;类脂生物合成抑制剂如乙酰基CoA羧化酶(ACCase)抑制剂;或oxynil(即溴苯腈(bromoxynil)或碘苯腈(ioxynil))除草剂;此外,植物已经通过多次基因修饰而耐受多种类别除草剂,如耐受草甘膦和草铵膦二者或耐受草甘膦和选自ALS抑制剂、HPPD抑制剂、植物生长素抑制剂或ACCase抑制剂的另一类别除草剂二者。这些除草剂耐受性技术例如描述于Pest Management Science 61,2005,246;61,2005,258;61,2005,277;61,2005,269;61,2005,286;64,2008,326;64,2008,332;Weed Science57,2009,108;Australian Journal of Agricultural Research 58,2007,708;Science316,2007,1185;以及其中引用的文献中。几种栽培植物已经通过基因突变和常规育种方法耐受除草剂,例如耐受咪唑啉酮类如咪草啶酸(imazamox)的夏播油菜(Canola,德国BASF SE)或耐受磺酰脲类,例如苯黄隆(tribenuron)的向日葵(DuPont,USA)。已经使用基因工程方法来赋予栽培植物如大豆、棉花、玉米、甜菜和油菜对除草剂如草甘膦、咪唑啉酮类和草铵膦的耐受性,它们中的一些正在开发或者可以以牌号或商标名(耐受草甘膦,Monsanto,U.S.A.)、(耐受咪唑啉酮,德国BASF SE)和(耐受草铵膦,德国Bayer CropScience)市购。
此外,还包括通过使用重组DNA技术而能够合成一种或多种杀虫蛋白,尤其是由芽孢杆菌属(Bacillus)细菌,特别是苏云金芽孢杆菌(Bacillus thuringiensis)已知的那些的植物,所述杀虫蛋白如δ-内毒素,例如CryIA(b),CryIA(c),CryIF,CryIF(a2),CryIIA(b),CryIIIA,CryIIIB(b1)或Cry9c;无性杀虫蛋白(VIP),例如VIP1、VIP2、VIP3或VIP3A;线虫定居细菌的杀虫蛋白,例如发光杆菌属(Photorhabdus)或致病杆菌属(Xenorhabdus);动物产生的毒素如蝎子毒素、蜘蛛毒素、黄蜂毒素或其他昆虫特异性神经毒素;真菌产生的毒素,例如链霉菌属(Streptomycetes)毒素;植物凝集素,例如豌豆或大麦凝集素;凝集素;蛋白酶抑制剂,例如胰蛋白酶抑制剂,丝氨酸蛋白酶抑制剂,patatin,半胱氨酸蛋白酶抑制剂或木瓜蛋白酶抑制剂;核糖体失活蛋白(RIP),例如蓖麻蛋白、玉米-RIP、相思豆毒蛋白、丝瓜籽蛋白、皂草素或异株腹泻毒蛋白(bryodin);类固醇代谢酶,例如3-羟基类固醇氧化酶、蜕皮甾类-IDP糖基转移酶、胆固醇氧化酶、蜕皮激素抑制剂或HMG-CoA还原酶;离子通道阻断剂,例如钠通道或钙通道阻断剂;保幼激素酯酶;利尿激素受体(helicokinin受体);茋合成酶,联苄合成酶,壳多糖酶或葡聚糖酶。在本发明上下文中,这些杀虫蛋白或毒素还具体理解为包括前毒素、杂合蛋白、截短的或其他方面改性的蛋白。杂合蛋白的特征在于蛋白域的新型组合(例如参见WO 02/015701)。该类毒素或能够合成这些毒素的基因修饰植物的其他实例公开于EP-A 374 753、WO 93/007278、WO 95/34656、EP-A 427529、EP-A 451878、WO03/18810和WO 03/52073中。生产这些基因修饰植物的方法对本领域熟练技术人员是已知的且例如公开于上述出版物中。这些含于基因修饰植物中的杀虫蛋白赋予产生这些蛋白的植物以对所有分类学上为节肢动物的害虫,尤其是甲虫(鞘翅目(Coleoptera))、双翅目昆虫(双翅目(Diptera))和蛾(鳞翅目(Lepidoptera))以及线虫(线虫纲(Nematoda))的耐受性。能够合成一种或多种杀虫蛋白的基因修饰植物例如描述于上述出版物中,它们中的一些可市购,例如(产生毒素Cry1Ab的玉米品种), Plus(产生毒素Cry1Ab和Cry3Bb1的玉米品种),(产生毒素Cry9c的玉米品种), RW(产生毒素Cry34Ab1、Cry35Ab1和酶膦丝菌素-N-乙酰转移酶[PAT]的玉米品种);33B(产生毒素Cry1Ac的棉花品种), I(产生毒素Cry1Ac的棉花品种), II(产生毒素Cry1Ac和Cry2Ab2的棉花品种);(产生VIP毒素的棉花品种);(产生毒素Cry3A的土豆品种); Bt11(例如 CB)和法国Syngenta Seeds SAS的Bt176(产生毒素Cry1Ab和PAT酶的玉米品种),法国Syngenta Seeds SAS的MIR604(产生毒素Cry3A的修饰译本的玉米品种,参见WO 03/018810),比利时Monsanto Europe S.A.的MON 863(产生毒素Cry3Bb1的玉米品种),比利时Monsanto Europe S.A.的IPC 531(产生毒素Cry1Ac的修饰译本的棉花品种)和比利时Pioneer Overseas Corporation的1507(产生毒素Cry1F和PAT酶的玉米品种)。
此外,还包括通过使用重组DNA技术能够合成一种或多种对细菌、病毒或真菌病原体的抗性或耐受性增强的蛋白质的植物。该类蛋白的实例是所谓的“与发病机理相关的蛋白”(PR蛋白,例如参见EP-A 392 225),植物病害抗性基因(例如表达针对来自墨西哥野生土豆Solanum bulbocastanum的致病疫霉(Phytophthora infestans)起作用的抗性基因的土豆品种)或T4溶菌酶(例如能够合成对细菌如Erwinia amylvora具有增强的抗性的这些蛋白的土豆品种)。生产这些基因修饰植物的方法对本领域熟练技术人员是已知的且例如公开于上述出版物中。
此外,还包括通过使用重组DNA技术能够合成一种或多种蛋白以提高产量(例如生物质产生、谷粒产量、淀粉含量、油含量或蛋白质含量),对干旱、盐或其他生长限制性环境因素的耐受性或对害虫以及真菌、细菌和病毒病原体的耐受性的植物。
此外,还包括通过使用重组DNA技术而含有改变量的成分含量或新成分含量以尤其改善人类或动物营养的植物,例如产生促进健康的长链ω-3脂肪酸或不饱和ω-9脂肪酸的油料作物(例如油菜,加拿大DOW Agro Sciences)。
此外,还包括通过使用重组DNA技术而含有改变量的成分含量或新成分含量以尤其改善原料生产的植物,例如产生增加量的支链淀粉的土豆(例如土豆,德国BASF SE)。
此外,已经发现本发明组合物还适于植物部分的脱叶和/或干燥,对此合适的是农作物如棉花、土豆、油籽油菜、向日葵、大豆或蚕豆,尤其是棉花。就此而言,已经发现用于植物干燥和/或脱叶的组合物、制备这些组合物的方法以及使用本发明组合物使植物干燥和/或脱叶的方法。
作为干燥剂,本发明组合物特别适于干燥农作物如土豆、油籽油菜、向日葵和大豆以及禾谷类的地上部分。这使得这些重要农作物的完全机械化收获成为可能。
还具有经济益处的是促进柑橘类水果、橄榄和其他品种的仁果、核果和坚果的收获,这通过在一定时间期限内集中裂开或降低对树的粘附而成为可能。相同的机理,即促进水果部分或叶部分与植物的枝部分之间产生脱离组织对于有用植物,尤其是棉花的受控脱叶也是必要的。
此外,各棉花植株成熟的时间间隔缩短导致收获后的纤维质量提高。
下列实施例用于说明本发明。
实施例
本发明组合物的除草作用由下列温室试验证实:
所用培养容器为含有含约2-3.0%有机物的壤质砂的塑料盆。对每一品种单独播种测试植物的种子。
对于出苗前处理,直接在播种之后借助细分布喷嘴施用悬浮或乳化于水中的活性化合物。温和灌溉容器以促进发芽和生长,然后用透明塑料罩覆盖,直到植物生根。该覆盖导致测试植物均匀发芽,除非这被活性化合物不利地影响。
对于出苗后处理,使测试植物生长到3-15cm的植物高度,这取决于植物习性,并仅在此时用悬浮或乳化于水中的活性化合物处理。为此,将测试植物直接播种并在相同容器中生长,或者首先使它们作为秧苗单独生长并在处理之前几天移植到测试容器中。
取决于品种,将植物分别保持在10-25℃和20-35℃下。
测试期为2-4周。在此期间照料植物并评价它们对各处理的响应。
使用0-100的评分进行评价。100表示没有植物出苗,或者至少地面上部分完全受损,而0表示没有损害,或者生长过程正常。对良好的除草活性给予至少70的分值,而对非常好的除草活性给予至少85的分值。
在下列实施例中使用S.R.Colby(1967)的方法“计算除草剂组合的协同增效和拮抗响应”,Weeds 15,第22页及随后各页,计算E值,其为各活性化合物的活性仅为加和时的预期值。
对于二元组合物:
E=X+Y-(X·Y/100)
其中
X=以施用率a使用活性化合物A的活性,%;
Y=以施用率b使用活性化合物B的活性,%;
E=A+B在施用率a+b下的预期活性(%)。
对于三元组合物:
其中
X=以施用率a使用活性化合物A的活性,%;
Y=以施用率b使用活性化合物B的活性,%;
Z=以施用率d使用活性化合物D的活性,%;
E=A+B+D在施用率a+b+d下的预期活性(%)。
若试验测定的值高于根据Colby计算的E值,则存在协同增效效果。
用于温室试验中的植物属于下列种类:
Bayer代码 | 学名 |
ABUTH | 苘麻(Abutilon theophrasti) |
AMBEL | 普通豚草(Ambrosia artemisiifolia) |
BRADC | 俯仰臂形草(Brachiaria decumbens) |
BRAPP | Urochloa platyphylla |
CHEAL | 藜(Chenopodium album) |
COMBE | 紫鸭趾草(Commelina benghalensis) |
CYPES | 油莎草(Cyperus esculentus) |
DIGSA | 马唐(Digitaria sanguinales) |
ECHCG | 稗草(Echinochloa crus-galli) |
ERBVI | 野黍(Eriochloa villosa) |
ERICA | 小蓬草(Erigeron canadensis) |
HELAN | 向日葵(Helianthus annuus) |
PANDI | 洋野黍(Panicum dichotomiflorun) |
PHACA | 金丝雀虉草(Phalaris canariensis L.) |
PHBPU | 圆叶牵牛(Pharbitis purpurea) |
POLPE | 蓼(Polygonum persicaria) |
注:100-90%:“非常好”;90-80%:“良好”。
这些试验的结果下文在应用实施例中给出并证实包含至少一种选自a1)-a6)的除草剂A和至少一种除草剂B的混合物的协同增效效果。就此而言,a.i.是指活性成分,基于100%活性成分。
为了制备混合物,除草剂A以包含22.5重量%相应除草剂A的水溶液形式使用。除草剂B和D以如下所示相应市售配制剂形式使用。1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(B.14)以10重量%悬浮浓缩物形式使用。合适的话,将助剂 HC加入该混合物中。
HC为含有脂肪酸酯和烷氧基化醇-磷酸酯的可乳化浓缩物。
将活性成分的相应混合物引入用于施用活性化合物的喷雾液中。在实施例中,所用溶剂为水。
实施例1:cornexistin(a1))+异丙基铵盐形式的草甘膦(B.26)的混合物的出苗后处理
实施例2:cornexistin(a1)+topramezone(B.25)的混合物的出苗后处理:
实施例3:cornexistin(a1))+二甲铵盐形式的麦草畏(B.32)的混合物的出苗后处理:
实施例4:cornexistin(a1))+苯嘧磺草胺(B.12)+1重量% HC的混合物的出苗后处理:
实施例5:cornexistin(a1))+indaziflam(B.28)+1重量% HC的混合物的出苗后处理:
实施例6:cornexistin(a1))+1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(B.14)+1重量% HC的混合物的出苗后处理:
实施例7:cornexistin(a1))+二氯化物形式的对草快(B.6)+1重量% HC的混合物的出苗后处理:
实施例8:cornexistin(a1))+铵盐形式的草铵膦(B.27)+1重量% HC的混合物的出苗后处理:
实施例9:cornexistin(a1))+topramezone(B.25)+莠去津(D.3)的混合物的出苗后处理
实施例10:cornexistin(a1))+炔草酯(B.2)+喹氧乙酸(cloquinocet-mexyl)(C2)的混合物的出苗后处理
实施例11:cornexistin(a1))+氟酮唑草(B.7)的混合物的出苗后处理
实施例12:cornexistin(a1))+氟酮唑草(B.7)+异丙基铵盐形式的草甘膦(B.26)的混合物的出苗后处理:
Claims (17)
1.一种除草组合物,包含:
A)Cornexistin(I.a1):
包括其可农用盐;
以及
B)至少一种选自除草剂炔草酯(B.2)、对草快(B.6)、氟酮唑草(B.7)、苯嘧磺草胺(B.12)、1,5-二甲基-6-硫代-3-(2,2,7-三氟-3-氧代-4-(丙-2-炔基)-3,4-二氢-2H-苯并[b][1,4]嗪-6-基)-1,3,5-三嗪烷-2,4-二酮(B.14)、topramezone(B.25)、草甘膦(B.26)和草铵膦(B.27)组的其他活性化合物,
包括其可农用盐,
其中组分A与组分B的重量比A:B为1:75-75:1。
2.根据权利要求1的组合物,额外包含至少一种不同于除草剂A和B且选自莠去津(D.3)和草甘膦(B.26)的其他除草剂D。
3.根据权利要求1或2的组合物,额外包含至少一种安全剂C。
4.根据权利要求3的组合物,其中组分A与组分C的重量比A:C为1:75-75:1,并且组分B与组分C的重量比B:C为1:75-75:1。
5.根据权利要求3的组合物,其中组分A与组分B的总和与组分C的重量比(A+B):C为1:75-75:1。
6.根据权利要求4的组合物,其中组分A与组分B的总和与组分C的重量比(A+B):C为1:75-75:1。
7.根据权利要求2的组合物,其中组分A与组分D的重量比A:D为1:75-75:1,并且组分B与组分D的重量比B:D为1:75-75:1。
8.根据权利要求2或7的组合物,其中组分A与与组分B的总和与组分D的重量比(A+B):D为1:75-75:1。
9.根据权利要求3的组合物,其中组分A与组分C的重量比A:C为1:75-75:1,组分A与组分D的重量比A:D为1:75-75:1,组分B与组分C的重量比B:C为1:75-75:1,组分B与组分D的重量比B:D为1:75-75:1,并且组分C与组分D的重量比C:D为1:75-75:1。
10.根据权利要求3的组合物,其中组分A与组分B的总和与组分C的重量比(A+B):C为1:75-75:1,并且组分A与组分B的总和与组分D的重量比(A+B):D为1:75-75:1。
11.根据权利要求9的组合物,其中组分A与组分B的总和与组分C的重量比(A+B):C为1:75-75:1,并且组分A与组分B的总和与组分D的重量比(A+B):D为1:75-75:1。
12.根据权利要求3的组合物,其中组分A、组分B和组分D的总和与组分C的重量比(A+B+D):C为1:75-75:1。
13.根据权利要求9的组合物,其中组分A、组分B和组分D的总和与组分C的重量比(A+B+D):C为1:75-75:1。
14.根据权利要求10的组合物,其中组分A、组分B和组分D的总和与组分C的重量比(A+B+D):C为1:75-75:1。
15.一种农业化学组合物,包含除草活性量的根据权利要求1-14中任一项的组合物和至少一种惰性液体和/或固体载体以及合适的话至少一种表面活性物质。
16.一种制备根据权利要求15的农业化学组合物的方法,包括将除草活性量的根据权利要求1-14中任一项的除草组合物和至少一种惰性液体和/或固体载体以及合适的话至少一种表面活性物质混合。
17.一种防治不希望的植物生长的方法,包括使除草活性量的根据权利要求1-14中任一项的除草组合物或根据权利要求15的农业化学组合物作用于植物、其环境或种子上。
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US201261747374P | 2012-12-31 | 2012-12-31 | |
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EP13171653.2 | 2013-06-12 | ||
EP13171653 | 2013-06-12 | ||
PCT/EP2013/076464 WO2014102069A1 (en) | 2012-12-31 | 2013-12-13 | Herbicidal composition |
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CN105072902B true CN105072902B (zh) | 2017-08-01 |
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JP (1) | JP6317761B2 (zh) |
KR (1) | KR20150103208A (zh) |
CN (1) | CN105072902B (zh) |
BR (1) | BR112015015779A2 (zh) |
CR (1) | CR20150397A (zh) |
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WO (1) | WO2014102069A1 (zh) |
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JP6325572B2 (ja) * | 2012-12-31 | 2018-05-16 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | コルネキスチンを含む除草組成物 |
BR112016023853A2 (pt) | 2014-04-17 | 2017-08-15 | Basf Se | composto, composição, método para controlar a vegetação indesejável e uso de um composto |
WO2015197392A1 (en) * | 2014-06-25 | 2015-12-30 | Basf Se | Herbicidal compositions comprising cornexistin and/or hydroxycornexistin |
EP3209668B1 (en) | 2014-10-24 | 2018-07-25 | Basf Se | Substituted pyridine compounds having herbicidal activity |
CN108041050A (zh) * | 2017-12-15 | 2018-05-18 | 北京科发伟业农药技术中心 | 含唑啉草酯和苯嘧磺草胺的除草组合物 |
BR112021008676A2 (pt) * | 2018-12-07 | 2021-08-10 | Sumitomo Chemical Company, Limited | composição herbicida e método de controle de ervas daninhas |
JP7179645B2 (ja) * | 2019-02-25 | 2022-11-29 | 日本曹達株式会社 | 除草方法 |
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JP2644818B2 (ja) * | 1987-04-27 | 1997-08-25 | 三共株式会社 | 新規化合物コーネギスチンおよびその用途ならびにその製造法 |
US4897104A (en) * | 1987-04-27 | 1990-01-30 | Sankyo Company Limited | Anhydride herbicides |
JPH02256602A (ja) * | 1988-10-24 | 1990-10-17 | Sankyo Co Ltd | 除草剤組成物 |
US5424278A (en) * | 1994-03-01 | 1995-06-13 | Dowelanco | Hydroxycornexistin |
AR008158A1 (es) * | 1996-09-05 | 1999-12-09 | Syngenta Participations Ag | Proceso para el control de malas hierbas en cultivos de plantas utiles que son resistentes a un fosfo-herbicida y una composicion herbicida para dicho uso. |
DK1226127T3 (da) * | 2000-05-04 | 2009-10-19 | Basf Se | Substituerede phenylsulfamoylcarboxamider |
JP2005068121A (ja) * | 2003-08-27 | 2005-03-17 | Maruwa Biochemical Co Ltd | 速効性微粒除草剤 |
DE102005031789A1 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Gmbh | Kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide Safener |
AR080234A1 (es) * | 2010-02-25 | 2012-03-21 | Marrone Bio Innovations Inc | Cepa bacteriana aislada del genero burkholderia y metabolitos pesticidas del mismo |
JP6325572B2 (ja) * | 2012-12-31 | 2018-05-16 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | コルネキスチンを含む除草組成物 |
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2013
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- 2013-12-13 WO PCT/EP2013/076464 patent/WO2014102069A1/en active Application Filing
- 2013-12-13 CN CN201380073897.4A patent/CN105072902B/zh not_active Expired - Fee Related
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CN105072902A (zh) | 2015-11-18 |
JP2016501911A (ja) | 2016-01-21 |
BR112015015779A2 (pt) | 2017-07-11 |
JP6317761B2 (ja) | 2018-04-25 |
PH12015501429A1 (en) | 2015-09-07 |
US20150342193A1 (en) | 2015-12-03 |
KR20150103208A (ko) | 2015-09-09 |
WO2014102069A1 (en) | 2014-07-03 |
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