JP2015535809A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015535809A5 JP2015535809A5 JP2015528642A JP2015528642A JP2015535809A5 JP 2015535809 A5 JP2015535809 A5 JP 2015535809A5 JP 2015528642 A JP2015528642 A JP 2015528642A JP 2015528642 A JP2015528642 A JP 2015528642A JP 2015535809 A5 JP2015535809 A5 JP 2015535809A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- membered
- nitrogen
- optionally substituted
- oxygen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 52
- 229920006395 saturated elastomer Polymers 0.000 claims description 38
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 34
- 125000005842 heteroatom Chemical group 0.000 claims description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 229910052760 oxygen Inorganic materials 0.000 claims description 32
- 239000001301 oxygen Chemical group 0.000 claims description 32
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 30
- 229910052717 sulfur Chemical group 0.000 claims description 30
- 239000011593 sulfur Chemical group 0.000 claims description 30
- 125000000623 heterocyclic group Chemical group 0.000 claims description 17
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 14
- 229920000515 polycarbonate Polymers 0.000 claims description 14
- 239000004417 polycarbonate Substances 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 14
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- 150000004696 coordination complex Chemical class 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 6
- 239000001569 carbon dioxide Substances 0.000 claims description 6
- 150000002118 epoxides Chemical class 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 125000003367 polycyclic group Chemical group 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 238000004587 chromatography analysis Methods 0.000 claims description 4
- 125000001072 heteroaryl group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 239000003446 ligand Substances 0.000 claims description 4
- VEUMANXWQDHAJV-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]ethyliminomethyl]phenol Chemical compound OC1=CC=CC=C1C=NCCN=CC1=CC=CC=C1O VEUMANXWQDHAJV-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000005587 carbonate group Chemical group 0.000 claims description 2
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical group [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- 238000010276 construction Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- 125000005549 heteroarylene group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002346 iodo group Chemical group I* 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 125000005647 linker group Chemical group 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 125000001620 monocyclic carbocycle group Chemical group 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 238000001556 precipitation Methods 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims 1
- 150000004679 hydroxides Chemical class 0.000 claims 1
- 150000002823 nitrates Chemical class 0.000 claims 1
- 235000021317 phosphate Nutrition 0.000 claims 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000000909 amidinium group Chemical group 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261693000P | 2012-08-24 | 2012-08-24 | |
| US61/693,000 | 2012-08-24 | ||
| PCT/US2013/056102 WO2014031811A1 (en) | 2012-08-24 | 2013-08-22 | Metal complexes |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018004171A Division JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015535809A JP2015535809A (ja) | 2015-12-17 |
| JP2015535809A5 true JP2015535809A5 (https=) | 2016-09-29 |
| JP6313305B2 JP6313305B2 (ja) | 2018-04-18 |
Family
ID=50150376
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015528642A Active JP6313305B2 (ja) | 2012-08-24 | 2013-08-22 | 金属錯体 |
| JP2018004171A Withdrawn JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018004171A Withdrawn JP2018052995A (ja) | 2012-08-24 | 2018-01-15 | 金属錯体 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9771388B2 (https=) |
| EP (1) | EP2888271B1 (https=) |
| JP (2) | JP6313305B2 (https=) |
| KR (1) | KR102096761B1 (https=) |
| CN (1) | CN104781268B (https=) |
| ES (1) | ES2761880T3 (https=) |
| WO (1) | WO2014031811A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102128706B1 (ko) | 2008-08-22 | 2020-07-02 | 사우디 아람코 테크놀로지스 컴퍼니 | 촉매 및 중합체 합성방법 |
| EP2707353B1 (en) | 2011-05-13 | 2021-03-31 | Novomer, Inc. | Carbonylation catalysts and method |
| KR102024510B1 (ko) | 2011-07-18 | 2019-11-14 | 사우디 아람코 테크놀로지스 컴퍼니 | 금속 착체 |
| WO2013067460A1 (en) | 2011-11-04 | 2013-05-10 | Novomer, Inc. | Metal complexes for the copolymerization of carbon dioxide and epoxides |
| US9403861B2 (en) | 2011-12-11 | 2016-08-02 | Novomer, Inc. | Salen complexes with dianionic counterions |
| EP2888271B1 (en) | 2012-08-24 | 2019-11-06 | Saudi Aramco Technologies Company | Metal complexes |
| WO2019126221A1 (en) | 2017-12-22 | 2019-06-27 | Saudi Aramco Technologies Company | Catalysts for polycarbonate production |
| JP2021522355A (ja) | 2018-04-18 | 2021-08-30 | サウジ アラムコ テクノロジーズ カンパニー | ポリ(アルキレンカーボネート)ポリマーの末端基異性化 |
| WO2020028606A1 (en) | 2018-08-02 | 2020-02-06 | Saudi Aramco Technologies Company | Sustainable polymer compositions and methods |
| MA53727A (fr) | 2018-09-24 | 2021-12-29 | Saudi Aramco Tech Co | Copolymères séquencés de polycarbonate et procédés associés |
| TWI906317B (zh) | 2020-06-24 | 2025-12-01 | 沙烏地阿拉伯商沙烏地阿美科技公司 | 多元醇組合物及方法 |
| WO2022153149A1 (en) | 2021-01-12 | 2022-07-21 | Saudi Aramco Technologies Company | Continuous manufacturing of polyol |
| US12195576B2 (en) | 2021-06-23 | 2025-01-14 | Saudi Aramco Technologies Company | Polyol compositions and methods |
Family Cites Families (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69128528T2 (de) | 1990-03-21 | 1998-07-30 | Res Corp Technologies Inc | Chirale katalysatoren und dadurch katalysierte epoxydierungsreaktionen |
| US5637739A (en) | 1990-03-21 | 1997-06-10 | Research Corporation Technologies, Inc. | Chiral catalysts and catalytic epoxidation catalyzed thereby |
| US5696109A (en) | 1992-12-07 | 1997-12-09 | Eukarion, Inc. | Synthetic catalytic free radical scavengers useful as antioxidants for prevention and therapy of disease |
| US6030917A (en) | 1996-07-23 | 2000-02-29 | Symyx Technologies, Inc. | Combinatorial synthesis and analysis of organometallic compounds and catalysts |
| US5665890A (en) | 1995-03-14 | 1997-09-09 | President And Fellows Of Harvard College | Stereoselective ring opening reactions |
| WO1998004538A1 (en) | 1996-07-26 | 1998-02-05 | Princeton University | Catalytic oxygenation of hydrocarbons by metalloporphyrin and metallosalen complexes |
| TWI246520B (en) | 1997-04-25 | 2006-01-01 | Mitsui Chemicals Inc | Processes for olefin polymerization |
| US6130340A (en) | 1998-01-13 | 2000-10-10 | President And Fellows Of Harvard College | Asymmetric cycloaddition reactions |
| US6521561B1 (en) | 1998-05-01 | 2003-02-18 | President And Fellows Of Harvard College | Main-group metal based asymmetric catalysts and applications thereof |
| KR100342659B1 (en) | 2000-12-15 | 2002-07-04 | Rstech Co Ltd | Chiral polymer salene catalyst and process for preparing chiral compounds from racemic epoxide using the same |
| US6884750B2 (en) | 2001-06-27 | 2005-04-26 | Rs Tech Corp. | Chiral salen catalyst and methods for the preparation of chiral compounds from racemic epoxides by using new catalyst |
| US6639087B2 (en) | 2001-08-22 | 2003-10-28 | Rhodia Pharma Solutions Inc. | Kinetic resolution method |
| DE10235316A1 (de) | 2002-08-01 | 2004-02-12 | Basf Ag | Katalysator und Verfahren zur Carbonylierung von Oxiranen |
| US7304172B2 (en) * | 2004-10-08 | 2007-12-04 | Cornell Research Foundation, Inc. | Polycarbonates made using highly selective catalysts |
| KR100724550B1 (ko) | 2004-12-16 | 2007-06-04 | 주식회사 엘지화학 | 이중 금속 아연 착화합물과 이를 촉매로 사용한폴리카보네이트의 제조 방법 |
| WO2006099162A2 (en) | 2005-03-14 | 2006-09-21 | Georgia Tech Research Corporation | Polymeric salen compounds and methods thereof |
| US7399822B2 (en) | 2005-06-21 | 2008-07-15 | Cornell Research Foundation, Inc. | Isotactic specific catalyst for direct production of highly isotactic poly (propylene oxide) or highly isotactic poly (butylene oxide) |
| GB0607096D0 (en) | 2006-04-07 | 2006-05-17 | Imp Innovations Ltd | Compound |
| US8232267B2 (en) | 2006-10-06 | 2012-07-31 | The Trustees Of Princeton University | Porphyrin catalysts and methods of use thereof |
| GB0708016D0 (en) | 2007-04-25 | 2007-06-06 | Univ Newcastle | Synthesis of cyclic carbonates |
| EP2573126B1 (en) | 2007-05-04 | 2014-09-24 | SK Innovation Co. Ltd. | A process for producing polycarbonates and a coordination complex used therefor |
| WO2008150033A1 (ja) | 2007-06-08 | 2008-12-11 | The University Of Tokyo | エポキシドと二酸化炭素との立体選択的交互共重合 |
| EP2096132A1 (en) | 2008-02-26 | 2009-09-02 | Total Petrochemicals Research Feluy | Monomers issued from renewable resources and process for polymerising them |
| BRPI0908982B8 (pt) | 2008-03-07 | 2018-08-07 | Univ Newcastle | síntese de carbonatos cíclicos |
| CN104193980B (zh) | 2008-05-09 | 2018-11-13 | 康奈尔大学 | 环氧乙烷与二氧化碳的聚合物 |
| US7858729B2 (en) | 2008-05-29 | 2010-12-28 | Novomer, Inc. | Methods of controlling molecular weight distribution of polymers and compositions thereof |
| CA2727959A1 (en) | 2008-07-30 | 2010-02-04 | Sk Energy, Co., Ltd. | Novel coordination complexes and process of producing polycarbonate by copolymerization of carbon dioxide and epoxide using the same as catalyst |
| KR102128706B1 (ko) | 2008-08-22 | 2020-07-02 | 사우디 아람코 테크놀로지스 컴퍼니 | 촉매 및 중합체 합성방법 |
| CN103333330A (zh) | 2008-09-08 | 2013-10-02 | 诺沃梅尔公司 | 聚碳酸酯多元醇组合物和方法 |
| WO2010033703A1 (en) | 2008-09-17 | 2010-03-25 | Novomer, Inc. | Purification of polycarbonates |
| CA2639870A1 (en) | 2008-09-29 | 2010-03-29 | Nova Chemicals Corporation | Trimerization |
| US8580911B2 (en) | 2008-11-01 | 2013-11-12 | Novomer, Inc. | Polycarbonate block copolymers |
| CN101412809B (zh) * | 2008-11-28 | 2011-04-27 | 大连理工大学 | 用于合成聚碳酸酯的单活性点催化剂 |
| GB0904654D0 (en) * | 2009-03-18 | 2009-04-29 | Univ Newcastle | Synthesis of cyclic carbonates |
| KR101221404B1 (ko) | 2009-06-18 | 2013-01-11 | 아주대학교산학협력단 | 이산화탄소/에폭사이드 공중합 촉매 시스템 |
| CN102665406B (zh) | 2009-12-24 | 2016-03-09 | 诺沃梅尔公司 | 合成多环胍化合物的方法 |
| KR101503745B1 (ko) | 2010-02-25 | 2015-03-19 | 에스케이이노베이션 주식회사 | 나이트레이트 음이온의 이산화탄소/에폭사이드 공중합 촉매 시스템 |
| WO2011163133A1 (en) | 2010-06-20 | 2011-12-29 | Novomer, Inc. | Aliphatic polycarbonates |
| KR101983006B1 (ko) | 2010-08-27 | 2019-05-29 | 사우디 아람코 테크놀로지스 컴퍼니 | 중합체 조성물 및 방법 |
| EP2609090A4 (en) | 2010-08-28 | 2013-12-25 | Novomer Inc | AMMONIC ACID ANHYDRIDE FROM ETHYLENE OXIDE |
| KR101805648B1 (ko) | 2010-09-14 | 2017-12-14 | 사우디 아람코 테크놀로지스 컴퍼니 | 중합체 합성용의 촉매 및 방법 |
| KR101963568B1 (ko) | 2010-09-22 | 2019-07-31 | 사우디 아람코 테크놀로지스 컴퍼니 | 치환된 살리실알데하이드 유도체의 합성 |
| EP3584265B1 (en) | 2010-11-23 | 2023-03-15 | Saudi Aramco Technologies Company | Polycarbonate polyol compositions |
| US8952104B2 (en) | 2011-01-06 | 2015-02-10 | Novomer, Inc. | Polymer compositions and methods |
| CN103687584B (zh) * | 2011-01-28 | 2016-03-30 | 罗地亚管理公司 | 表现出低眼刺激潜能的个人清洁体系 |
| HUE036462T2 (hu) | 2011-05-09 | 2018-07-30 | Saudi Aramco Tech Co | Polimer készítmények és eljárások |
| EP2707353B1 (en) | 2011-05-13 | 2021-03-31 | Novomer, Inc. | Carbonylation catalysts and method |
| KR102024510B1 (ko) | 2011-07-18 | 2019-11-14 | 사우디 아람코 테크놀로지스 컴퍼니 | 금속 착체 |
| IN2014CN01299A (https=) | 2011-07-25 | 2015-04-24 | Novomer Inc | |
| KR20190059988A (ko) | 2011-08-08 | 2019-05-31 | 사우디 아람코 테크놀로지스 컴퍼니 | 폴리머 합성용 촉매 및 방법 |
| GB201115565D0 (en) | 2011-09-08 | 2011-10-26 | Imp Innovations Ltd | Method of synthesising polycarbonates in the presence of a bimetallic catalyst and a chain transfer agent |
| WO2013055747A1 (en) | 2011-10-10 | 2013-04-18 | Novomer, Inc. | Methods to produce alkylated polycyclic guanidine compounds |
| WO2013067460A1 (en) | 2011-11-04 | 2013-05-10 | Novomer, Inc. | Metal complexes for the copolymerization of carbon dioxide and epoxides |
| US9403861B2 (en) | 2011-12-11 | 2016-08-02 | Novomer, Inc. | Salen complexes with dianionic counterions |
| WO2013096602A1 (en) | 2011-12-20 | 2013-06-27 | Novomer, Inc. | Methods for polymer synthesis |
| CN102558199B (zh) * | 2011-12-31 | 2014-10-22 | 中国科学院长春应用化学研究所 | 四齿席夫碱金属配合物、金属卟啉配合物和制备聚碳酸酯的方法 |
| WO2013138161A1 (en) | 2012-03-12 | 2013-09-19 | Novomer, Inc. | Polymer compositions and methods |
| EP2838954B1 (en) | 2012-04-16 | 2024-09-18 | Saudi Aramco Technologies Company | Adhesive compositions and methods |
| US20140024795A1 (en) | 2012-04-25 | 2014-01-23 | Novomer, Inc. | Aliphatic polycarbonate polyols containing silyl groups |
| JP6527080B2 (ja) | 2012-05-24 | 2019-06-05 | サウジ アラムコ テクノロジーズ カンパニー | ポリカーボネートポリオール組成物および方法 |
| EP2888271B1 (en) | 2012-08-24 | 2019-11-06 | Saudi Aramco Technologies Company | Metal complexes |
-
2013
- 2013-08-22 EP EP13830629.5A patent/EP2888271B1/en active Active
- 2013-08-22 US US14/422,780 patent/US9771388B2/en active Active
- 2013-08-22 KR KR1020157007284A patent/KR102096761B1/ko active Active
- 2013-08-22 CN CN201380053750.9A patent/CN104781268B/zh active Active
- 2013-08-22 WO PCT/US2013/056102 patent/WO2014031811A1/en not_active Ceased
- 2013-08-22 ES ES13830629T patent/ES2761880T3/es active Active
- 2013-08-22 JP JP2015528642A patent/JP6313305B2/ja active Active
-
2017
- 2017-08-22 US US15/683,496 patent/US20170349616A1/en not_active Abandoned
-
2018
- 2018-01-15 JP JP2018004171A patent/JP2018052995A/ja not_active Withdrawn
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015535809A5 (https=) | ||
| JP2013539802A5 (https=) | ||
| JP6313305B2 (ja) | 金属錯体 | |
| Khandar et al. | Anion influence in the structural diversity of cadmium coordination polymers constructed from a pyridine based Schiff base ligand | |
| Cheng et al. | Coordination polymers constructed from an adaptable pyridine-dicarboxylic acid linker: assembly, diversity of structures, and catalysis | |
| Singh et al. | Solvent-induced carboxylate shift and movement of an anthryl side-group in single-crystal to single-crystal structural dynamics in a gadolinium coordination polymer | |
| Ay et al. | Hydrothermal synthesis, crystal structure and heterogeneous catalytic activity of a novel inorganic–organic hybrid complex, possessing infinite La–O–La linkages | |
| Zhang et al. | Coordination polymers driven by carboxy functionalized picolinate linkers: Hydrothermal Assembly, structural multiplicity, and catalytic features | |
| Liang et al. | Anion-dependent assemblies of a series of Cd (II) coordination complexes based on an asymmetric multi-dentate ligand and inorganic SBUs: syntheses, crystal structures, and fluorescent properties | |
| Jurowska et al. | Vanadium precursors and the type of complexes formed with Schiff base ligand composed of 5-bromosalicylaldehyde and 2-hydroxybenzhydrazide–Structure and characterization | |
| Sanram et al. | Ni (II)-metal–organic frameworks based on 1, 4-phenylenedipropionic acid: Solvothermal syntheses, structures, and photocatalytic properties | |
| Yeh et al. | Roles of the anion in the self-assembly of silver (I) complexes containing 4-amino-1, 2, 4-triazole | |
| Thapa et al. | Co (II) coordination polymers exhibiting reversible structural transformation and color change: A comparative analysis with Ni (II) analogue | |
| Yaman et al. | Hydrothermal synthesis and characterization of cobalt (II), nickel (II) and zinc (II) coordination polymers with 2, 2′-dimethylglutarate and 1, 2-bis (4-pyridyl) ethane | |
| Mishra et al. | Four novel isostructural coordination polymers {[M (H′ L) 2 (H2O) 2]· 2DMF}[M= Zn (II), Cd (II), Mn (II) and Co (II)] built using a nitrogen and oxygen donor azo ligand: Crystal structures and fluorescence studies | |
| Kar et al. | Synthesis and characterization of four novel manganese (II) chains formed by 4, 4′-azobis (pyridine) and benzoate or nitrobenzoates: Stabilization of unusual ladder structures | |
| Alim et al. | Synthesis and characterization of some metal complexes of Cu (II), Ni (II), Zn (II), Cd (II), Sn (II), Co (II), Sb (III) and Fe (III) containing bidentate Schiff base of Smdtc | |
| CN107207719B (zh) | 线型无机配位聚合物、金属络合物、金属纳米结构和包含其的催化剂组合物 | |
| Waheed | Synthesis and characterization of some metals complexes of {N-[(benzoyl amino)-thioxo methyl] proline} | |
| Dalai et al. | Combination of covalent and hydrogen bonding in the formation of 3D uranyl-carboxylate networks | |
| Kathalikkattil et al. | Synthesis, characterization and X-ray crystallographic investigation of 2-D hybrid hydrogen bonded and rectangular grid networks in Cu (II) and Co (II) metal complexes | |
| Wang et al. | Syntheses and structural characterization of three new coordination polymers of [Ag (PPIA)· H2O] n,[Cu (PPIA) 2· 2H2O] n and [Zn (PPIA) 2 (H2O) 2] n; PPIA= 3-pyridinepropionic acid | |
| Kim et al. | New topological 3D copper (ii) coordination networks: catechol oxidation catalysis and solvent adsorption via porous properties | |
| Pasynskii et al. | The role of inner-and outer-sphere ligands in pivalate and cymantrenecarboxylate complexes of transition metals | |
| Paul et al. | (μ-O, O′)-nitrito bridged 3-D coordination frameworks of M2+ (Mn Co, Zn) with mab and jsm topology |