JP2010184878A - Porous material - Google Patents
Porous material Download PDFInfo
- Publication number
- JP2010184878A JP2010184878A JP2009028722A JP2009028722A JP2010184878A JP 2010184878 A JP2010184878 A JP 2010184878A JP 2009028722 A JP2009028722 A JP 2009028722A JP 2009028722 A JP2009028722 A JP 2009028722A JP 2010184878 A JP2010184878 A JP 2010184878A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- porous material
- group
- polymer compound
- solid
- 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
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- 239000011148 porous material Substances 0.000 title claims abstract description 82
- 150000001875 compounds Chemical class 0.000 claims abstract description 40
- 229910052751 metal Inorganic materials 0.000 claims abstract description 31
- 239000002184 metal Substances 0.000 claims abstract description 29
- 239000003054 catalyst Substances 0.000 claims abstract description 24
- 239000007787 solid Substances 0.000 claims abstract description 24
- 239000011973 solid acid Substances 0.000 claims abstract description 22
- 239000013256 coordination polymer Substances 0.000 claims description 35
- 229920001795 coordination polymer Polymers 0.000 claims description 35
- 239000003446 ligand Substances 0.000 claims description 25
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 13
- 150000001735 carboxylic acids Chemical class 0.000 claims description 12
- 238000005259 measurement Methods 0.000 claims description 11
- 150000001491 aromatic compounds Chemical class 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 5
- 229910021645 metal ion Inorganic materials 0.000 claims description 5
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 5
- RAADBCJYJHQQBI-UHFFFAOYSA-N 2-sulfoterephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(S(O)(=O)=O)=C1 RAADBCJYJHQQBI-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 26
- 239000013110 organic ligand Substances 0.000 abstract description 8
- 229920000642 polymer Polymers 0.000 abstract description 4
- -1 sulfonated carbon (sulfonated activated carbon Chemical class 0.000 description 44
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 27
- 239000002253 acid Substances 0.000 description 25
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 24
- 238000000034 method Methods 0.000 description 16
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 14
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 125000001424 substituent group Chemical group 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 238000003786 synthesis reaction Methods 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- 239000011651 chromium Substances 0.000 description 10
- 238000009826 distribution Methods 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 229910052804 chromium Inorganic materials 0.000 description 8
- 238000004817 gas chromatography Methods 0.000 description 8
- 238000001179 sorption measurement Methods 0.000 description 8
- 229910052742 iron Inorganic materials 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000002411 thermogravimetry Methods 0.000 description 6
- 229910052720 vanadium Inorganic materials 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 229910021536 Zeolite Inorganic materials 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 5
- 238000005886 esterification reaction Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000010948 rhodium Substances 0.000 description 5
- 229910052707 ruthenium Inorganic materials 0.000 description 5
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 5
- 239000010457 zeolite Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 230000032050 esterification Effects 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000003456 ion exchange resin Substances 0.000 description 4
- 229920003303 ion-exchange polymer Polymers 0.000 description 4
- 238000004811 liquid chromatography Methods 0.000 description 4
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- 229910052703 rhodium Inorganic materials 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000007810 chemical reaction solvent Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- YQUVCSBJEUQKSH-UHFFFAOYSA-N protochatechuic acid Natural products OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- OXQOBQJCDNLAPO-UHFFFAOYSA-N 2,3-Dimethylpyrazine Chemical compound CC1=NC=CN=C1C OXQOBQJCDNLAPO-UHFFFAOYSA-N 0.000 description 2
- LCZUOKDVTBMCMX-UHFFFAOYSA-N 2,5-Dimethylpyrazine Chemical compound CC1=CN=C(C)C=N1 LCZUOKDVTBMCMX-UHFFFAOYSA-N 0.000 description 2
- 239000001934 2,5-dimethylpyrazine Substances 0.000 description 2
- HJFZAYHYIWGLNL-UHFFFAOYSA-N 2,6-Dimethylpyrazine Chemical compound CC1=CN=CC(C)=N1 HJFZAYHYIWGLNL-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- YPWLZGITFNGGKW-UHFFFAOYSA-N 2-phenanthrol Chemical compound C1=CC=C2C3=CC=C(O)C=C3C=CC2=C1 YPWLZGITFNGGKW-UHFFFAOYSA-N 0.000 description 2
- ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 2
- JOOXCMJARBKPKM-UHFFFAOYSA-N 4-oxopentanoic acid Chemical compound CC(=O)CCC(O)=O JOOXCMJARBKPKM-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- FINHMKGKINIASC-UHFFFAOYSA-N Tetramethylpyrazine Chemical compound CC1=NC(C)=C(C)N=C1C FINHMKGKINIASC-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000003463 adsorbent Substances 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- ROBFUDYVXSDBQM-UHFFFAOYSA-N hydroxymalonic acid Chemical compound OC(=O)C(O)C(O)=O ROBFUDYVXSDBQM-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- UNQNIRQQBJCMQR-UHFFFAOYSA-N phosphorine Chemical compound C1=CC=PC=C1 UNQNIRQQBJCMQR-UHFFFAOYSA-N 0.000 description 1
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- 235000019260 propionic acid Nutrition 0.000 description 1
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- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
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- 229940107700 pyruvic acid Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- SBYHFKPVCBCYGV-UHFFFAOYSA-N quinuclidine Chemical compound C1CC2CCN1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
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- 238000000926 separation method Methods 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
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- XSROQCDVUIHRSI-UHFFFAOYSA-N thietane Chemical compound C1CSC1 XSROQCDVUIHRSI-UHFFFAOYSA-N 0.000 description 1
- VOVUARRWDCVURC-UHFFFAOYSA-N thiirane Chemical compound C1CS1 VOVUARRWDCVURC-UHFFFAOYSA-N 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
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Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
本発明は、新規なブレンステッド酸性を有する多孔性材料及びその製造方法、及び該多孔性材料を用いた固体酸触媒に関する。 The present invention relates to a novel porous material having Bronsted acidity, a method for producing the same, and a solid acid catalyst using the porous material.
固体酸触媒は、塩酸や硫酸のような液状の酸に比べて、これを分離・回収するために中和や塩の除去といったプロセスが不要であり、不必要な副産物を生産することなく省エネルギーで目的物を得ることができるため、従来から積極的に研究が進められてきた。
その結果、ゼオライトやイオン交換樹脂、モンモリオナイト、シリカ−アルミナ、スルホン化カーボン（スルホン化活性炭）、スルホン基が固定化されたメソポーラスシリカ（スルホン酸化メソポーラスシリカ）等の固体酸触媒が知られており、石油化学品の製造及びさまざまな機能性材料の合成反応といったものに用いられている。しかしゼオライトやモンモリオナイトではスルホン酸基を有した固体酸性を示す材料は無く、スルホン化カーボン及びスルホン化メソポーラスシリカは、反応溶媒に対する耐久性や、反応溶媒に溶融してくる硫酸成分があり実際の使用は困難であった。
Compared with liquid acids such as hydrochloric acid and sulfuric acid, solid acid catalysts do not require processes such as neutralization and salt removal to separate and recover them, saving energy without producing unnecessary by-products. Since the object can be obtained, research has been actively conducted so far.
As a result, solid acid catalysts such as zeolite, ion exchange resin, montmorillonite, silica-alumina, sulfonated carbon (sulfonated activated carbon), and mesoporous silica (sulfonated mesoporous silica) with a fixed sulfone group are known. It is used for the production of petrochemicals and synthesis reactions of various functional materials. However, there is no solid acidity material with sulfonic acid groups in zeolite and montmorillonite, and sulfonated carbon and sulfonated mesoporous silica are actually resistant to the reaction solvent and have a sulfuric acid component that melts in the reaction solvent. The use of was difficult.
近年新しい多孔性材料として種々の配位形態をとりうる金属イオンと２座以上の配位座を有する架橋配位子とを組み合わせ自己集合させた配位高分子化合物が第３の多孔性材料として注目されている。配位高分子化合物はゼオライトと同様で均一な細孔を有するが、比表面積がゼオライトと比較し大きい（非特許文献１参照）、またスルホン酸基含有フッ素樹脂はガラス転移温度が低く耐熱性が低いが、配位高分子は高温でも安定である。さらにメソポーラスシリカのように合成過程でアミン系のテンプレートを使用しないため経済的である。 As a new porous material in recent years, a coordination polymer compound which is a self-assembled combination of a metal ion capable of various coordination forms and a bridging ligand having two or more coordination sites is a third porous material. Attention has been paid. The coordination polymer compound is similar to zeolite and has uniform pores, but the specific surface area is larger than that of zeolite (see Non-Patent Document 1), and the sulfonic acid group-containing fluororesin has a low glass transition temperature and heat resistance. Although low, coordination polymers are stable at high temperatures. Furthermore, unlike mesoporous silica, it is economical because no amine-based template is used in the synthesis process.
また、上記配位高分子化合物について、大表面積で耐熱性を有するような安定な骨格構造を形成させるには、カルボン酸系クラスター骨格のカルボン酸部位を芳香族化合物のカルボン酸で連結する方法が知られている（非特許文献２参照）。
特許文献１に記載の配位高分子化合物は、配位子がスルホン酸基を有する芳香族多価カルボン酸であるが、カルボン酸系クラスター骨格を有する金属と連結していない為、表面積が無い配位高分子化合物であり、細孔内触媒選択性が期待できる固体触媒にはなりえないものである。
In order to form a stable skeleton structure having a large surface area and heat resistance with respect to the coordination polymer compound, a method of linking the carboxylic acid portion of the carboxylic acid cluster skeleton with a carboxylic acid of an aromatic compound is a method. It is known (see Non-Patent Document 2).
The coordination polymer compound described in Patent Document 1 is an aromatic polyvalent carboxylic acid having a sulfonic acid group as a ligand, but has no surface area because it is not linked to a metal having a carboxylic acid cluster skeleton. It is a coordination polymer compound, and cannot be a solid catalyst that can be expected to have intra-pore catalyst selectivity.
従って、細孔が均一であり、非常に比表面積が大きく、耐熱性に優れ、固体酸性を有し、さらに合成が容易な多孔性材料は従来までに無く、新たな固体酸触媒として開発が期待されていた。 Therefore, porous materials with uniform pores, very large specific surface area, excellent heat resistance, solid acidity, and easy synthesis are unprecedented and are expected to be developed as new solid acid catalysts. It had been.
本発明は、細孔が均一であり、非常に比表面積が大きく、耐熱性に優れ、固体酸性を有し、さらに合成が容易な多孔性材料を提供することを課題とする。また、前記多孔性材料を有する固体酸触媒の提供を課題とする。 An object of the present invention is to provide a porous material having uniform pores, a very large specific surface area, excellent heat resistance, solid acidity, and easy synthesis. Another object is to provide a solid acid catalyst having the porous material.
本発明者らは、上記課題を解決すべく鋭意検討した結果、所定量以上の表面積を有し、かつ細孔径が均一で耐熱性を有する固体酸性を有する多孔性材料により達成されることを見出した。
即ち、本発明は、
ＢＥＴ比表面積が８００ｍ２／ｇ以上、細孔径が均一、及び耐熱温度が１００℃以上で、固体酸量０．１ｍｍｏｌ／ｇ以上の固体酸性を有する多孔性材料からなるものである。
As a result of intensive studies to solve the above problems, the present inventors have found that this is achieved by a porous material having a solid acidity having a surface area of a predetermined amount or more, a uniform pore diameter, and heat resistance. It was.
That is, the present invention
It is made of a porous material having a solid acidity with a BET specific surface area of 800 m 2 / g or more, a uniform pore diameter, a heat resistant temperature of 100 ° C. or more, and a solid acid amount of 0.1 mmol / g or more.
本発明の固体酸性を有する多孔性材料は、熱安定性に優れ、細孔が均一であり、比表面積が大きく、また製造が容易である為、新規固体酸触媒として有用である。また水に安定である為、エステル化反応、アセトンとフェノールの縮合によるＢＰＡ製造反応、ラクタム化合物の製造反応等の酸を必要とする反応に適している。
また比表面積が大きく、極性基を有する為、水蒸気やメタン、二酸化炭素、水素などのガス吸蔵材としても適している。
The porous material having solid acidity of the present invention is useful as a novel solid acid catalyst because it is excellent in thermal stability, has uniform pores, has a large specific surface area, and is easy to produce. Moreover, since it is stable in water, it is suitable for reactions requiring an acid such as esterification reaction, BPA production reaction by condensation of acetone and phenol, and lactam compound production reaction.
In addition, since it has a large specific surface area and a polar group, it is also suitable as a gas storage material for water vapor, methane, carbon dioxide, hydrogen and the like.
（固体酸性を有する多孔性材料）
本発明の多孔性材料は耐熱性に優れ、比表面積が大きく、均一な細孔径を有し、且つ固体酸性を有する。具体的には、ＢＥＴ比表面積が８００ｍ２／ｇ以上、細孔径が均一、耐熱温度が１００℃以上で、固体酸量０．１ｍｍｏｌ／ｇ以上の固体酸性を有する多孔性材料である。
(Porous material with solid acidity)
The porous material of the present invention has excellent heat resistance, a large specific surface area, a uniform pore diameter, and solid acidity. Specifically, it is a porous material having a solid acidity with a BET specific surface area of 800 m 2 / g or more, a uniform pore diameter, a heat resistant temperature of 100 ° C. or more, and a solid acid amount of 0.1 mmol / g or more.
本発明において多孔性材料とは、多数の細孔を有する固体物質を意味する。本発明の多孔性材料は、比表面積が、多点法ＢＥＴ比表面積として８００ｍ２／ｇ以上、詳細には、
８００〜５０００ｍ２／ｇであり、好ましくは１０００〜４０００ｍ２／ｇ、更に好ましくは１２００〜３０００ｍ２／ｇのものである。比表面積が大きいほど細孔が大きくなるため触媒としての反応性が優れるという点で好ましいが、もろくて安定性に欠ける材料になりやすい。
In the present invention, the porous material means a solid substance having a large number of pores. The porous material of the present invention has a specific surface area of 800 m 2 / g or more as a multipoint BET specific surface area.
800~5000m a 2 / g, and preferably those 1000~4000m 2 / g, more preferably of 1200~3000m 2 / g. The larger the specific surface area, the larger the pores, which is preferable in terms of excellent reactivity as a catalyst. However, the material tends to be brittle and lacks stability.
また、本発明の多孔性材料は細孔が均一であることを特徴とする。ここでいう均一とは、細孔径分布曲線における最大ピークを示す細孔直径の±４０％の範囲に全細孔容積の６０％以上が含まれることを意味し、更に好ましくは細孔直径の±２０％の範囲に全細孔容積の６０％以上が含まれることをいう。細孔径分布曲線は次に述べる方法により求めることができる。すなわち、多孔性材料を液体窒素温度（７７．４Ｋ）にて冷却して窒素ガスを導入し、定容量法あるいは重量法によりその吸着量を求め、次いで導入する窒素ガスの圧力を徐々に増幅させ、各平衡に対する窒素ガスの吸着量をプロットし、吸着等温線を得る。この吸着等温線を用いて、ＣＩ法、ＤＨ法、ＢＪＨ法の計算法により細孔径分布曲線を求めることができる。 The porous material of the present invention is characterized by uniform pores. The term “uniform” as used herein means that 60% or more of the total pore volume is included in the range of ± 40% of the pore diameter showing the maximum peak in the pore size distribution curve, and more preferably ±± of the pore diameter. It means that 60% or more of the total pore volume is included in the range of 20%. The pore size distribution curve can be determined by the method described below. That is, the porous material is cooled at a liquid nitrogen temperature (77.4 K), nitrogen gas is introduced, the adsorption amount is obtained by a constant volume method or a gravimetric method, and then the pressure of the introduced nitrogen gas is gradually amplified. Then, the adsorption amount of nitrogen gas for each equilibrium is plotted to obtain an adsorption isotherm. Using this adsorption isotherm, a pore size distribution curve can be obtained by the calculation method of CI method, DH method, and BJH method.
本発明の多孔性材料のように細孔径が均一である材料では、活性炭など分布のある材料と比較して特異的な立体選択性などが期待できるため好ましい。
また、本発明の多孔性材料は、耐熱温度が１００℃以上である。上記耐熱温度は、例えば、熱重量分析（ＴＧ）測定することによって吸着水の脱離以外の重量減少を測定することにより多孔性材料の骨格が分解する温度として測定することができる。固体酸触媒として利用する上で耐熱性は重要であり、既存の例えばイオン交換樹脂などは１００℃以上での利用は困難である。本明細書中で耐熱温度とは、吸着水が脱離したと考えられる温度（１００℃）を基準にして５ｗｔ％重量減少した温度を意味する。本発明の多孔性材料の耐熱温度は１００〜４００℃が好ましく、耐熱温度が高温であるほど利用できる触媒反応が増える為、２００〜４００℃がより好ましい。
A material having a uniform pore diameter, such as the porous material of the present invention, is preferable because a specific stereoselectivity can be expected as compared with a material having a distribution such as activated carbon.
Moreover, the heat resistant temperature of the porous material of the present invention is 100 ° C. or higher. The heat-resistant temperature can be measured, for example, as a temperature at which the skeleton of the porous material is decomposed by measuring weight loss other than desorption of adsorbed water by thermogravimetric analysis (TG) measurement. Heat resistance is important for use as a solid acid catalyst, and existing ion exchange resins, for example, are difficult to use at 100 ° C. or higher. In the present specification, the heat-resistant temperature means a temperature reduced by 5 wt% based on the temperature (100 ° C.) at which adsorbed water is considered to be desorbed. The heat resistant temperature of the porous material of the present invention is preferably 100 to 400 ° C., and the higher the heat resistant temperature, the more catalytic reaction that can be used, so 200 to 400 ° C. is more preferable.
本発明の多孔性材料の固体酸量は、０．１ｍｍｏｌ／ｇ以上であり、１０ｍｍｏｌ／ｇ以下であることが好ましい。さらに好ましくは０．５〜５ｍｍｏｌ／ｇであり、酸価が低すぎると活性作用が低く固体酸としての作用が低くなり易く、１０ｍｍｏｌ／ｇを超えて高すぎると極性溶媒に可溶し固体酸としての機能が損なわれ易い。
本発明の多孔性材料の固体酸量は、滴定法により求めることができる。例えば、スルホン酸基を含む多孔性材料を所定の濃度の塩化ナトリウム水溶液に分散させた後、所定の濃度の水酸化ナトリウム水溶液で滴定することによって、固体酸量を求めることができる。
また、本発明の多孔性材料は、Ｘ線波長１．５４１８４ÅのＣｕ−Ｋα線による粉末Ｘ線回折測定において、少なくとも３．３°±０．３°、８．４°±０．３°及び９．０°±０．３°の回折角（２θ）に回折ピークを有する特徴を有する。
The solid acid amount of the porous material of the present invention is 0.1 mmol / g or more and preferably 10 mmol / g or less. More preferably, it is 0.5 to 5 mmol / g. If the acid value is too low, the active action is low and the action as a solid acid tends to be low, and if it exceeds 10 mmol / g, the solid acid is soluble in a polar solvent. The function as is easily impaired.
The solid acid amount of the porous material of the present invention can be determined by a titration method. For example, the amount of solid acid can be determined by dispersing a porous material containing a sulfonic acid group in a sodium chloride aqueous solution having a predetermined concentration and titrating with a sodium hydroxide aqueous solution having a predetermined concentration.
Further, the porous material of the present invention has at least 3.3 ° ± 0.3 °, 8.4 ° ± 0.3 °, and 8.4 ° ± 0.3 ° in powder X-ray diffraction measurement with Cu-Kα ray having an X-ray wavelength of 1.54184 mm. It has the characteristic of having a diffraction peak at a diffraction angle (2θ) of 9.0 ° ± 0.3 °.
（配位高分子化合物）
上記固体酸性を有する多孔性材料は、例えば、以下の配位高分子化合物により構成されるものが挙げられる。本明細書において、配位高分子化合物とは、金属元素と有機配位子の反応により得られる高分子化合物で、その主鎖の繰り返し単位（以下、「構成単位」と称することがある）が配位結合によって結合しているものをいう。
(Coordination polymer compound)
Examples of the porous material having solid acidity include those composed of the following coordination polymer compounds. In this specification, the coordination polymer compound is a polymer compound obtained by a reaction between a metal element and an organic ligand, and has a repeating unit of the main chain (hereinafter sometimes referred to as “structural unit”). It is connected by a coordinate bond.
該配位高分子化合物の好ましい例としては、構成単位として、下記一般式（１）で表わされる２核金属クラスター、一般式（２）で表わされる３核金属クラスター、及び一般式（３）で表わされる４核金属クラスターのいずれかと、２つ以上のカルボン酸と１つ以上のスルホン酸基を有する配位子からなるものが挙げられる。
｛Ｍ１（ＯＯＣ−Ｒ−ＣＯＯ）｝２ ・・・（１）
（式中、Ｍ１はＣｕ２＋、Ｒｈ２＋、Ｚｎ２＋、Ｍｏ２＋、Ｃｒ２＋、Ｃｏ２＋から選
択される２価の金属イオンを表わす。Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表し、他の置換基により置換されていてもよい。）
｛Ｍ２ ３Ｏ（ＯＯＣ−Ｒ−ＣＯＯ）３｝ ・・・（２）
（式中、Ｍ２はＣｒ３＋、Ｒｕ３＋、Ｆｅ３＋、Ｍｎ３＋、Ｖ３＋、Ｔｉ３＋、Ｃｏ３＋から選択される３価の金属イオンを表わす。Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表し、他の置換基により置換されていてもよい。）
｛Ｚｎ４Ｏ（ＯＯＣ−Ｒ−ＣＯＯ）３｝ ・・・（３）
（式中、Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表し、他の置換基により置換されていてもよい。）
上記配位高分子化合物を構成する金属元素としては有機配位子と錯体を形成し得る金属元素であれば特に制限はなく、周期表のｓ−ブロック、ｐ−ブロック元素であるＢｅ、Ｍｇ、Ｃａ、Ｂａ、Ａｌ等も使用できるが、特にｄ−ブロック元素を使用することが好ましい。これは、配位高分子の形成には配位結合が重要な役割を担い、この配位結合の形成には、有機配位子が電子対を金属元素に供与し、この電子対を金属元素が受け入れるが、この電子対の受け入れにｄ軌道が適しているからである。
Preferred examples of the coordination polymer compound include, as structural units, a binuclear metal cluster represented by the following general formula (1), a trinuclear metal cluster represented by the general formula (2), and the general formula (3). One of the tetranuclear metal clusters represented, a ligand having two or more carboxylic acids and one or more sulfonic acid groups can be mentioned.
{M 1 (OOC-R-COO)} 2 (1)
(In the formula, M 1 represents a divalent metal ion selected from Cu 2+ , Rh 2+ , Zn 2+ , Mo 2+ , Cr 2+ , and Co 2+. R represents an aromatic compound having one or more sulfonic acid groups. And may be substituted with other substituents.
{M 2 3 O (OOC-R-COO) 3 } (2)
(In the formula, M 2 represents a trivalent metal ion selected from Cr 3+ , Ru 3+ , Fe 3+ , Mn 3+ , V 3+ , Ti 3+ , and Co 3+. R has one or more sulfonic acid groups. Represents an aromatic compound and may be substituted with other substituents.)
{Zn 4 O (OOC—R—COO) 3 } (3)
(In the formula, R represents an aromatic compound having one or more sulfonic acid groups, and may be substituted with other substituents.)
The metal element constituting the coordination polymer compound is not particularly limited as long as it is a metal element capable of forming a complex with an organic ligand, and Be, Mg, which are s-block and p-block elements of the periodic table. Ca, Ba, Al and the like can be used, but it is particularly preferable to use a d-block element. This is because coordination bonds play an important role in the formation of coordination polymers, and organic ligands donate electron pairs to metal elements for the formation of coordination bonds. This is because the d-orbital is suitable for accepting this electron pair.
ｄ−ブロック元素としては、有機配位子と複合錯体を形成し得る元素であれば特に制限はないが、形成される有機無機複合体の安定性、結晶性の点から、Ｔｉ、Ｖ、Ｃｒ、Ｍｎ、Ｆｅ、Ｃｏ、Ｃｕ、Ｚｎ、Ｍｏ、Ｒｕ、Ｒｈ、よりなる群から選ばれることが好ましく、特にＣｏ、Ｃｕ、Ｆｅ、Ｒｕ、Ｚｎ、Ｒｈよりなる群から選ばれることが好ましい。またこれらの構成する金属元素は１種類からなることが多いが、２種類以上の混合金属でもかまわない。 The d-block element is not particularly limited as long as it is an element capable of forming a complex complex with an organic ligand. However, from the viewpoint of stability and crystallinity of the formed organic-inorganic complex, Ti, V, Cr , Mn, Fe, Co, Cu, Zn, Mo, Ru, Rh, and preferably selected from the group consisting of Co, Cu, Fe, Ru, Zn, and Rh. These constituent metal elements are often composed of one kind, but two or more kinds of mixed metals may be used.
上記配位高分子化合物を構成する金属元素は単核でも良いがクラスター化していることがより好ましく、２核、３核、４核、６核、８核、１２核の金属から構成されるいずれのクラスターでもかまわない。クラスター源となる金属は金属単体及び金属酸化物、過塩素酸塩、蟻酸塩、酢酸塩、硝酸塩、塩化塩、硫酸塩など金属塩または水和塩、いずれの形態を用いてもよい。 The metal element constituting the coordination polymer compound may be mononuclear, but more preferably clustered, and any of the metal composed of two, three, four, six, eight, or twelve nuclei is preferable. You can also use other clusters. As the metal that serves as the cluster source, any form of simple metal and metal oxide, perchlorate, formate, acetate, nitrate, chloride, sulfate, and other metal salts or hydrates may be used.
クラスターを構成する要素としてハロゲンブリッジ、酸素、水酸基ブリッジ、チオールブリッジ、硫酸基ブリッジ、カルボン酸ブリッジ等がある。以下に２核クラスター構造例（一般式（４））、３核クラスター構造例（一般式（５））、カルボン酸クラスターの構造例（一般式（６））、及びスルホン酸クラスターの構造例（一般式（７））を示す。 Examples of elements constituting the cluster include a halogen bridge, oxygen, a hydroxyl group bridge, a thiol bridge, a sulfate group bridge, and a carboxylic acid bridge. The following is a binuclear cluster structure example (general formula (4)), a trinuclear cluster structure example (general formula (5)), a carboxylic acid cluster structural example (general formula (6)), and a sulfonic acid cluster structural example ( Formula (7)) is shown.
（式中、Ｍは金属、Ｘはハロゲン元素、酸素、水酸基（ＯＨ）、チオール（ＳＨ、Ｓ−Ｒ（Ｒはアルキル基を示す））を示す。 ） (In the formula, M represents a metal, X represents a halogen element, oxygen, a hydroxyl group (OH), and a thiol (SH, S—R (R represents an alkyl group)).)
(式中、Ｍは金属、Ｘはハロゲン元素、酸素、水酸基（ＯＨ）、チオール（ＳＨ、Ｓ−
Ｒ（Ｒはアルキル基を示す））を示す。）
(Wherein M is a metal, X is a halogen element, oxygen, hydroxyl group (OH), thiol (SH, S-
R (R represents an alkyl group)). )
(式中、Ｍは金属、Ｒはアルキル基を示す。) (In the formula, M represents a metal and R represents an alkyl group.)
（式中、Ｍは金属を示す。）
２核クラスターの中では、図１に示す様な上記一般式（１）で表わされる構造をとるカルボン酸型クラスターが安定性の面より好ましい。２核カルボン酸型クラスターを構成する金属種としては、銅、ロジウム、亜鉛、モリブデン、クロム、コバルトが含まれ、銅、ロジウム、モリブデンを含有するクラスターが安定性の面より好ましい。
(In the formula, M represents a metal.)
Among the binuclear clusters, a carboxylic acid type cluster having a structure represented by the general formula (1) as shown in FIG. 1 is preferable from the viewpoint of stability. The metal species constituting the dinuclear carboxylic acid type cluster includes copper, rhodium, zinc, molybdenum, chromium, and cobalt, and a cluster containing copper, rhodium, and molybdenum is preferable from the viewpoint of stability.
３核クラスターの中では図２に示す様な一般式（２）で表わされる構造をとるカルボン酸型クラスターが好ましい。３核カルボン酸型クラスターを構成する金属種としては、クロム、ルテニウム、鉄、マンガン、バナジウム、コバルト、チタンが含まれる。クロム、バナジウム、ルテニウム、鉄を含有するクラスターが安定性の面より好ましい。
さらに４核クラスターとしては、図３に示す様な一般式（３）で表わされる構造をとるカルボン酸型クラスターが好ましい。
Among the trinuclear clusters, a carboxylic acid type cluster having a structure represented by the general formula (2) as shown in FIG. 2 is preferable. Metal species constituting the trinuclear carboxylic acid type cluster include chromium, ruthenium, iron, manganese, vanadium, cobalt, and titanium. A cluster containing chromium, vanadium, ruthenium, and iron is preferable from the viewpoint of stability.
Further, the tetranuclear cluster is preferably a carboxylic acid type cluster having a structure represented by the general formula (3) as shown in FIG.
いずれのカルボン酸型クラスターとカルボン酸系配位子でも大表面積錯体が形成されるが水蒸気安定性の関係から特に３核クラスター構造がもっとも好ましく、構成する金属種としては、クロム、ルテニウム、鉄、マンガン、バナジウム、コバルト、チタンが含まれるが、合成錯体の安定性の観点よりクロム元素が最も好ましい。
配位高分子化合物の配位子は、非共有電子対を持つものが好ましく、配位高分子を形成させるには１４族及び１５族の元素を含んだ有機配位子が好ましい。特に、ヘテロ元素として、Ｎ、Ｏ、Ｐ、Ｓの１種又は２種以上を有する有機配位子が好ましい。
Although any carboxylic acid type cluster and carboxylic acid type ligand form a large surface area complex, a trinuclear cluster structure is most preferable from the viewpoint of water vapor stability, and the constituent metal species include chromium, ruthenium, iron, Manganese, vanadium, cobalt, and titanium are included, but chromium element is most preferable from the viewpoint of the stability of the synthetic complex.
The ligand of the coordination polymer compound preferably has an unshared electron pair, and an organic ligand containing a group 14 or group 15 element is preferable for forming the coordination polymer. In particular, an organic ligand having one or more of N, O, P, and S as a hetero element is preferable.
このようなヘテロ元素を有する有機配位子としては特に制限はないが、下記の化合物に由来するＮ、Ｏ、Ｐ、Ｓの１種又は２種以上を含有する構造を有するものが好ましい。
Ｎ含有構造としては、ピロール、イミダゾール、ピラゾール、ピリジン、ピリダジン、ピリミジン、ピラジン、２−ピロリン、２−ピラゾリン、ピラゾリジン、インドール、インドリジン、キノリン、イソキノリン、４Ｈ−キノリジン、プリン、１Ｈ−インダゾール、キナゾリン、シンノリン、キノキサリン、フタラジン、プテリジン、カルバゾール、アクリジン、フェナントリジン、フェナジン、インドリン、イソインドリン、１,２,３−トリアジン、１,２,４−トリアジン、１,３,５−トリアジン、１,２,３−トリアゾール、１,２,４−トリアゾール、テトラキス［（２,４−ジアミノ−１,３,５−トリアゾ−６−イル）フェニル］メタン、２,２’−ビピリジン、４,４’−ビピリジン、１,２−ビス（２−ピリジル）エタン、１,２−ビス（２−ピリジル）エチレン、１,２−ビス（２−ピリジル）グリコール、１,２−ビス（４−ピリジル）エタン、１,２−ビス（４−ピリジル）エチレン、１,２−ビス（４−ピリジル）グリコール、テトラメチルピラジン、２,３−ジメチルピラジン、２,５−ジメチルピラジン、２,６−ジメチルピラジン、２,４,６−トリ（４−ピリジル）−１,３,５−トリアジン、２,２’−ビイミダゾールなどの含窒素芳香族複素環系化合物、ピロリジン、２−イミダゾリドン、イミダゾリジン、ピペリジン、ピペラジン、キヌクリジン、アジリジン、アゼピンなどの含窒素脂肪族環状化合物が挙げられる。
Although there is no restriction | limiting in particular as an organic ligand which has such a hetero element, What has a structure containing 1 type, or 2 or more types of N, O, P, S derived from the following compound is preferable.
N-containing structures include pyrrole, imidazole, pyrazole, pyridine, pyridazine, pyrimidine, pyrazine, 2-pyrroline, 2-pyrazoline, pyrazolidine, indole, indolizine, quinoline, isoquinoline, 4H-quinolidine, purine, 1H-indazole, quinazoline Cinnoline, quinoxaline, phthalazine, pteridine, carbazole, acridine, phenanthridine, phenazine, indoline, isoindoline, 1,2,3-triazine, 1,2,4-triazine, 1,3,5-triazine, 1, 2,3-triazole, 1,2,4-triazole, tetrakis [(2,4-diamino-1,3,5-triazo-6-yl) phenyl] methane, 2,2'-bipyridine, 4,4 ' -Bipyridine, 1,2-bis (2-pyridyl) ethane, 1,2-bis (2-pi Lysyl) ethylene, 1,2-bis (2-pyridyl) glycol, 1,2-bis (4-pyridyl) ethane, 1,2-bis (4-pyridyl) ethylene, 1,2-bis (4-pyridyl) Glycol, tetramethylpyrazine, 2,3-dimethylpyrazine, 2,5-dimethylpyrazine, 2,6-dimethylpyrazine, 2,4,6-tri (4-pyridyl) -1,3,5-triazine, 2, Nitrogen-containing aromatic heterocyclic compounds such as 2′-biimidazole, and nitrogen-containing aliphatic cyclic compounds such as pyrrolidine, 2-imidazolidone, imidazolidine, piperidine, piperazine, quinuclidine, aziridine, and azepine.
また、Ｎを含む置換基も好ましく、アミノ基、シアノ基、アミド基、イミノ基、ニトロ基等が挙げられ、これらの置換基を有する化合物も好ましい。このような化合物としては、例えば、１,３,５−トリス（３―エチニルベンゾニトリル）ベンゼン、３−シアノ−６−メチル−２（１Ｈ）ピリジノン、４,４’,４’’−４’’’−テトラシアノテトラフェニルメタン等が挙げられる。 A substituent containing N is also preferable, and examples thereof include an amino group, a cyano group, an amide group, an imino group, and a nitro group. Examples of such a compound include 1,3,5-tris (3-ethynylbenzonitrile) benzene, 3-cyano-6-methyl-2 (1H) pyridinone, 4,4 ′, 4 ″ -4 ′. '' -Tetracyanotetraphenylmethane and the like.
含有構造としては、特に制限はないが、カルボン酸類、オキソ化合物類、アルコール類が好ましい。カルボン酸の場合、１分子中にあるカルボキシル基の数に応じて、モノカルボン酸、ジカルボン酸、トリカルボン酸などと総称されるが、勿論、カルボキシル基の数には何ら限定されるものではなく、テトラカルボン酸、ペンタカルボン酸、ヘキサカルボン酸等のポリカルボン酸を用いても良い。カルボン酸類としては、例えば、ギ酸、酢酸、プロピオン酸、酪酸、イソ酪酸、吉草酸、イソ吉草酸、ピバル酸、ラウリン酸、ミリスチン酸、パルミチン酸、ステアリン酸、シュウ酸、マロン酸、コハク酸、グルタル酸、アジピン酸、ピメリン酸、スベリン酸、ゼライン酸、セバシン酸、アクリル酸、プロピオル酸、メタクリル酸、クロトン酸、イソクロトン酸、オレイン酸、エライジン酸、マレイン酸、フマル酸、シトラコン酸、メサコン酸、ショウノウ酸などの飽和または不飽和脂肪族のカルボン酸、安息香酸、フタル酸、イソフタル酸、テレフタル酸、トリメシン酸、ピロメリット酸、メリット酸、ナフトエ酸、トルイル酸、ヒドロアトロパ酸、ケイ皮酸、フル酸、テン酸などの芳香族炭化水素または複素環化合物のカルボン酸、グリコール酸、乳酸、グリセリン酸、タルトロン酸、リンゴ酸、酒石酸などの水酸基含有の飽和または不飽和脂肪族のカルボン酸、トロパ酸、ベンジル酸、サリチル酸、アニス酸、バニリン酸、ベラトル酸、ピペロニル酸、プロトカテキュ酸、没食子酸などの水酸基含有芳香族炭化水素系カルボン酸、グリオキシル酸、ピルビン酸、アセト酢酸、メソシュウ酸、オキサル酢酸、レブリン酸などのカルボニル基含有カルボン酸等が挙げられる。 The containing structure is not particularly limited, but carboxylic acids, oxo compounds, and alcohols are preferable. In the case of carboxylic acid, depending on the number of carboxyl groups in one molecule, it is generically named monocarboxylic acid, dicarboxylic acid, tricarboxylic acid, etc. Of course, the number of carboxyl groups is not limited at all, Polycarboxylic acids such as tetracarboxylic acid, pentacarboxylic acid, and hexacarboxylic acid may be used. Examples of carboxylic acids include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, lauric acid, myristic acid, palmitic acid, stearic acid, oxalic acid, malonic acid, succinic acid, Glutaric acid, adipic acid, pimelic acid, suberic acid, xelinic acid, sebacic acid, acrylic acid, propiolic acid, methacrylic acid, crotonic acid, isocrotonic acid, oleic acid, elaidic acid, maleic acid, fumaric acid, citraconic acid, mesaconic acid , Saturated or unsaturated aliphatic carboxylic acids such as camphoric acid, benzoic acid, phthalic acid, isophthalic acid, terephthalic acid, trimesic acid, pyromellitic acid, merit acid, naphthoic acid, toluic acid, hydroatropic acid, cinnamic acid, Aromatic hydrocarbons or heterocyclic compounds such as fluoric acid and tenoic acid Hydroxyl-containing saturated or unsaturated aliphatic carboxylic acids such as oxalic acid, lactic acid, glyceric acid, tartronic acid, malic acid, tartaric acid, tropic acid, benzylic acid, salicylic acid, anisic acid, vanillic acid, veratric acid, piperonic acid And hydroxyl group-containing aromatic hydrocarbon carboxylic acids such as protocatechuic acid and gallic acid, and carbonyl group-containing carboxylic acids such as glyoxylic acid, pyruvic acid, acetoacetic acid, mesooxalic acid, oxalacetic acid, and levulinic acid.
水酸基含有化合物類としては特に制限はないが、フェノール、ピロカテコール、レゾルシノール、ピロガロール、フロログリシノール、チモール、カルバクロール、スチフニン酸、２−ナフトール、２−フェナントロール、１、２、４−ベンゼントリオール、ｐ−ターフェニル−２’−オール、ヒドロキノン、９、１０−ビス（３、５−ジヒドロキシフェニル）アントラセン、ビスフェノールＡ等のフェノール類が挙げられる。 There are no particular restrictions on the hydroxyl group-containing compounds, but phenol, pyrocatechol, resorcinol, pyrogallol, phloroglicinol, thymol, carvacrol, stiffnic acid, 2-naphthol, 2-phenanthrol, 1,2,4-benzenetriol , P-terphenyl-2′-ol, hydroquinone, 9,10-bis (3,5-dihydroxyphenyl) anthracene, bisphenol A and other phenols.
Ｓ含有構造として、特に制限はないが、チイラン、チイレン、チエタン、チエテン、チオフェン、チオラン、１、３−チアゾール、ベンゾチオフェン、１、４−ジチアナフタレン等が挙げられる。これらのうち、特に好ましいのは、チオフェン、チオラン、１、３−チアゾール等である。
Ｐ含有構造として、特に制限はないが、ホスファベンゼン、トリフェニルホスフィン、トリフェニルホスフィンオキシド、リン酸及びリン酸エステル類、亜リン酸及び亜リン酸エステル類、次亜リン酸及び次亜リン酸エステル類等が挙げられる。これらのうち、特に好ましいのは、トリフェニルホスフィン、リン酸、リン酸エステル類等である。また上記配位子は組み合わせて使用しても良い。
The S-containing structure is not particularly limited, and examples thereof include thiirane, thylene, thietane, thieten, thiophene, thiolane, 1,3-thiazole, benzothiophene, and 1,4-dithiaphthalene. Of these, thiophene, thiolane, 1,3-thiazole and the like are particularly preferable.
The P-containing structure is not particularly limited, but phosphabenzene, triphenylphosphine, triphenylphosphine oxide, phosphoric acid and phosphoric acid esters, phosphorous acid and phosphorous acid esters, hypophosphorous acid and hypophosphorous acid Examples include acid esters. Of these, triphenylphosphine, phosphoric acid, phosphoric acid esters and the like are particularly preferable. The above ligands may be used in combination.
固体酸性の発現にはスルホン酸、りん酸、カルボン酸何れでも良いが、固体酸性度からスルホン酸がより好ましい。
上記配位高分子を形成する配位子の中で、２つ以上のカルボン酸と１つ以上のスルホン酸基を有する芳香族化合物が良く、ベンゼン、ナフタレン、ビフェニル、フェナントレン、アントラセン、ピレン、１、３、５−トリフェニルベンゼンなど剛直な部位を有し、２つ以上のカルボン酸と１つ以上のスルホン酸基を有する図４及び図５に示す構造を有する配位子から選択されたものが好ましく用いられる。さらに、具体的には、例えば、図６に記載の化合物が配位子として集積化させ易い点で好ましく、その中でも最も好ましくは２−スルホテレフタル酸である。
For the expression of solid acidity, any of sulfonic acid, phosphoric acid and carboxylic acid may be used, but sulfonic acid is more preferable from the viewpoint of solid acidity.
Among the ligands forming the coordination polymer, aromatic compounds having two or more carboxylic acids and one or more sulfonic acid groups are preferable, such as benzene, naphthalene, biphenyl, phenanthrene, anthracene, pyrene, Selected from ligands having the structure shown in FIGS. 4 and 5 having a rigid site such as 3,5-triphenylbenzene and having two or more carboxylic acids and one or more sulfonic acid groups Is preferably used. More specifically, for example, the compound shown in FIG. 6 is preferable in that it can be easily integrated as a ligand, and 2-sulfoterephthalic acid is most preferable among them.
上記配位子のカルボン酸、スルホン酸以外の部位は他の置換基、以下の３つのいずれの置換基を有しても良い。（ｉ）１〜１０個の炭素原子からなる置換または無置換の炭化水素基。（ｉｉ）１〜１０個の炭素原子からなる置換または無置換のアルコキシ基、または、置換または無置換のアリーロキシ基及びヘテロアリーロキシ基。（ｉｉｉ）その他置換基（ｉ）〜（ｉｉｉ）において、置換基は、アルキル基、ハロアルキル基、シクロアルキル基、アリール基、シアノ基、ニトロ基、ハロゲン原子、アルコキシ基、カルボアルコキシ基、シリル基及びシロキシ基より成る群より選定される置換基である。 Sites other than the carboxylic acid and sulfonic acid of the ligand may have other substituents and any of the following three substituents. (I) A substituted or unsubstituted hydrocarbon group consisting of 1 to 10 carbon atoms. (Ii) A substituted or unsubstituted alkoxy group consisting of 1 to 10 carbon atoms, or a substituted or unsubstituted aryloxy group and heteroaryloxy group. (Iii) Other substituents (i) to (iii), the substituent is an alkyl group, haloalkyl group, cycloalkyl group, aryl group, cyano group, nitro group, halogen atom, alkoxy group, carboalkoxy group, silyl group. And a substituent selected from the group consisting of siloxy groups.
（ｉ）における具体例としては、メチル基、エチル基、ｎ−プロピル基、イソプロピル基、ｎ−ブチル基、ｓ−ブチル基、ｔ−ブチル基、ｎ−ペンチル基、イソペンチル基、ネオペンチル基、ｔ−ペンチル基、ｔ−ヘキシル基等の炭素数１〜１０の直鎖または分岐のアルキル基、シクロプロピル基、シクロヘキシル基、シクロオクチル基、アダマンチル基のような炭素数３〜１０のシクロアルキル基が挙げられる。 Specific examples of (i) include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, t-butyl group, n-pentyl group, isopentyl group, neopentyl group, t A cycloalkyl group having 3 to 10 carbon atoms such as a linear or branched alkyl group having 1 to 10 carbon atoms such as a pentyl group or a t-hexyl group, a cyclopropyl group, a cyclohexyl group, a cyclooctyl group or an adamantyl group; Can be mentioned.
（ｉｉ）における具体例としては、メトキシ基、エトキシ基、ｔｅｒｔ−ブトキシ基等の飽和炭化水素基から成るアルコシキ基、フェノキシ基、１−ナフトキシ基、２−ナフトキシ基、メトキシフェノキシ基、ジメトキシフェノキシ基、カルボメトキシフェノキシ基、シアノフェノキシ基、ニトロフェノキシ基、クロロフェノキシ基、ジクロロフェノキシ基、ペンタフルオロフェノキシ基、メチルフェノキシ基、エチルフェノキシ基、ジメチルフェノキシ基、トリフルオロメチルフェノキシ基、メチルナフトキシ基、メトキシナフトキシ基、クロロナフトキシ基、ニトロナフトキシ基、テトラヒドロナフトキシ基等の置換基を有していてもよいアリーロキシ基、ベンジロキシ基等のアラルキルオキシ基、ピ
リジノキシ基、メチルピリジノキシ基、ニトロピリジノキシ基、ピラジロキシ基、ピリミジロキシ基、ベンゾフリロキシ基、キノリロキシ基、イソキノリロキシ基、ベンズイミダゾリロキシ基、インドリロキシ基等のヘテロ元素含有芳香族オキシ基等が挙げられる。カルボン酸、スルホン酸以外の部位は（ｉ）〜（ｉｉｉ）いずれの置換基により置換されていてもよいが細孔を大きく利用する上で立体的に小さい置換基であることが好ましい。
Specific examples in (ii) include alkoxy groups, phenoxy groups, 1-naphthoxy groups, 2-naphthoxy groups, methoxyphenoxy groups, dimethoxyphenoxy groups composed of saturated hydrocarbon groups such as methoxy groups, ethoxy groups, and tert-butoxy groups. Carbomethoxyphenoxy group, cyanophenoxy group, nitrophenoxy group, chlorophenoxy group, dichlorophenoxy group, pentafluorophenoxy group, methylphenoxy group, ethylphenoxy group, dimethylphenoxy group, trifluoromethylphenoxy group, methylnaphthoxy group, Aralkyloxy groups such as aryloxy groups and benzyloxy groups which may have substituents such as methoxynaphthoxy group, chloronaphthoxy group, nitronaphthoxy group, tetrahydronaphthoxy group, pyridinoxy group, methylpyridinoxy , Nitro pyridinoporphyrazine alkoxy group, Pirajirokishi group, Pirimijirokishi group, Benzofurirokishi group, Kinorirokishi group, Isokinorirokishi group, benzimidazolyl Lilo alkoxy group and a hetero atom-containing aromatic group, such as Indorirokishi group. Sites other than carboxylic acid and sulfonic acid may be substituted by any of the substituents (i) to (iii), but are preferably sterically small substituents when utilizing the pores.
本発明の配位高分子化合物の構成単位として好ましい例は、クラスター源として３核カルボン酸型クラスター、配位子として、ベンゼン、ナフタレン、ビフェニル、フェナントレン、アントラセン、ピレン、１，３，５−トリフェニルベンゼンなど剛直な部位を有し、２つ以上のカルボン酸と１つ以上のスルホン酸基を有する配位子からなるものが挙げられる。また、上記配位子の好適な例としては、図６に記載のものが挙げられる。 Preferred examples of the structural unit of the coordination polymer compound of the present invention include a trinuclear carboxylic acid type cluster as a cluster source, benzene, naphthalene, biphenyl, phenanthrene, anthracene, pyrene, 1,3,5-tris as a ligand. Examples thereof include phenylbenzene having a rigid site and having a ligand having two or more carboxylic acids and one or more sulfonic acid groups. Moreover, as a suitable example of the said ligand, the thing of FIG. 6 is mentioned.
さらに本発明の配位高分子化合物の構成単位としてもっとも好ましい例としては、クロムの２−スルホテレフタル酸錯体、鉄の２−スルホテレフタル酸錯体、バナジウムの２−スルホテレフタル酸錯体、ルテニウムの２−スルホテレフタル酸錯体、クロムの５−スルホイソテレフタル酸錯体、鉄の５−スルホイソテレフタル酸錯体、バナジウムの５−スルホイソテレフタル酸錯体、クロムの４−スルホイソテレフタル酸錯体、鉄の４−スルホイソテレフタル酸錯体、バナジウムの４−スルホイソテレフタル酸錯体が特に好ましい。 Further, the most preferable examples of the structural unit of the coordination polymer compound of the present invention include chromium 2-sulfoterephthalic acid complex, iron 2-sulfoterephthalic acid complex, vanadium 2-sulfoterephthalic acid complex, and ruthenium 2-sulfoterephthalic acid complex. Sulfoterephthalic acid complex, chromium 5-sulfoisoterephthalic acid complex, iron 5-sulfoisoterephthalic acid complex, vanadium 5-sulfoisoterephthalic acid complex, chromium 4-sulfoisoterephthalic acid complex, iron 4-sulfo Isoterephthalic acid complexes and vanadium 4-sulfoisoterephthalic acid complexes are particularly preferred.
（固体酸性を有する多孔性材料の製造方法）
本発明の固体酸性を有する多孔性材料は、上述の配位高分子化合物の構成要素である金属クラスター源、配位子、助触媒、溶媒を混合して拡散させるだけで得られることもあるが、ゼオライト合成と同様の方法でオートクレーブなどの耐圧容器に入れ高温・加圧下で反応させても良い。
(Method for producing porous material having solid acidity)
The porous material having solid acidity of the present invention may be obtained by simply mixing and diffusing a metal cluster source, a ligand, a promoter, and a solvent, which are constituent elements of the coordination polymer compound described above. Alternatively, it may be put in a pressure-resistant vessel such as an autoclave in the same manner as in zeolite synthesis and reacted at high temperature and pressure.
また反応する配位子のカルボン酸部位及びスルホン酸部位は共に、酸のままでもアルカリ金属塩化しても良い。混合比は２、３核クラスターでは配位子のカルボン酸量に対し金属カチオンがモル比として１：１程度が好ましく、４核クラスターでは配位子のカルボン酸量に対し金属カチオンがモル比として３：４程度を目安とするが、その比率よりをどちらかを過剰ないし大過剰に用いてもよい。 Further, both the carboxylic acid moiety and sulfonic acid moiety of the reacting ligand may be acid or alkali metal chloride. The mixing ratio is preferably about 1: 1 as the molar ratio of the metal cation to the amount of carboxylic acid of the ligand in a 2 or 3 nucleus cluster, and the molar ratio of the metal cation to the amount of carboxylic acid of the ligand in a 4 nucleus cluster. A ratio of about 3: 4 is used as a guide, but either of these ratios may be used in excess or large excess.
好ましくは配位子の量を多く入れた場合の方が得られる錯体の比表面積が大きくなることもあるが、経済的に良くない。
反応温度は、通常、常温〜３００℃の間である。反応温度が余りに高いときには生成物が分解する怖れがあるので、好ましくは、常温〜２５０℃である。
反応時間は、反応温度は合成のスケールによって一概には決められないが、低温であるほど長時間を要し、一般に３０分〜３週間である。反応を均一溶媒で実施する際は数時間程度で問題ないが、耐圧容器下、不均一条件で反応を実施する場合は長時間、具体的には１週間程度必要とする場合もある。
Preferably, the specific surface area of the complex obtained when the amount of the ligand is increased may be large, but it is not economically good.
The reaction temperature is usually between room temperature and 300 ° C. When the reaction temperature is too high, the product may be decomposed, so the temperature is preferably from room temperature to 250 ° C.
As for the reaction time, although the reaction temperature is not generally determined by the scale of synthesis, the lower the temperature, the longer it takes, generally 30 minutes to 3 weeks. When the reaction is carried out with a homogeneous solvent, there is no problem in about several hours. However, when the reaction is carried out under non-uniform conditions under a pressure vessel, it may take a long time, specifically about one week.
配位高分子化合物の合成反応をより促進させるため沸酸、塩酸、蟻酸、酢酸、硝酸など少量の酸や水酸化ナトリウムなどのアルカリを反応溶媒に加えてもよい。酸やアルカリは多量に用いると配位高分子化合物の合成を妨げる為、配位子に対して０．１〜１０倍モル、好ましくは１〜５倍モル程度が良い。溶媒に関しては水、有機溶媒いずれを使用しても良く混合させても良い。溶媒の使用量に関しては特に限定はないものの、重量基準で１０〜２０００倍程度が反応制御の容易さの点で好ましい。 In order to further promote the synthesis reaction of the coordination polymer compound, a small amount of acid such as boiling acid, hydrochloric acid, formic acid, acetic acid or nitric acid, or an alkali such as sodium hydroxide may be added to the reaction solvent. When an acid or alkali is used in a large amount, it interferes with the synthesis of the coordination polymer compound, so the amount is 0.1 to 10 times mol, preferably about 1 to 5 times mol for the ligand. Regarding the solvent, either water or an organic solvent may be used or mixed. Although there is no limitation in particular about the usage-amount of a solvent, about 10 to 2000 times on a weight basis is preferable at the point of the ease of reaction control.
反応終了後、沈殿物をろ過することによって、生成物を簡単に単離することができる。生成物単離後は、必要に応じ水や有機溶媒による洗浄を行う。好ましくは水とアセトンの等量混合溶液等用いることができる。また、単離された配位高分子化合物の陰イオンを交
換させる為に沸酸、塩酸、蟻酸、酢酸、硝酸など少量の酸に浸しても良い。
単離された生成物を吸着材として使用するためには、これを速やかに減圧下で加熱することによって、脱溶媒することが特に好ましい。脱溶媒することにより配位高分子化合物が安定化して多孔質構造が維持される傾向にある。その加熱温度は、５０〜３５０℃程度が好適である。なお脱溶媒せずに長時間、例えば数日間放置すると、配位高分子化合物の結晶構造が変わり、比表面積が減少し吸着材、触媒としての性能を損ねる怖れがある。
After completion of the reaction, the product can be easily isolated by filtering the precipitate. After isolation of the product, washing with water or an organic solvent is performed as necessary. Preferably, a mixed solution of equal amounts of water and acetone can be used. Further, in order to exchange the anion of the isolated coordination polymer compound, it may be immersed in a small amount of acid such as boiling acid, hydrochloric acid, formic acid, acetic acid, nitric acid.
In order to use the isolated product as an adsorbent, it is particularly preferred to remove the solvent by rapidly heating it under reduced pressure. By removing the solvent, the coordination polymer compound is stabilized and the porous structure tends to be maintained. The heating temperature is preferably about 50 to 350 ° C. If the solvent is left for a long time without removing the solvent, for example, for several days, the crystal structure of the coordination polymer compound is changed, the specific surface area is decreased, and the performance as an adsorbent or catalyst may be impaired.
（多孔性材料の形状及び触媒としての利用）
このような本発明の固体酸性を有する多孔性材料の形状は、特に制限されないが、触媒として利便上、粒子状或いは膜状であることが好ましい。形状が粒子状の場合、粒子の平均粒径は０．０１〜１００μｍであることが好ましく、０．０１〜５０μｍであることがより好ましく、０．１〜５０μｍであることが特に好ましい。触媒の平均粒径が０．０１μｍ未満である場合は、粒子が飛散しやすく取り扱いが困難となる傾向にあり、他方、平均粒径が１００μｍを超える場合は、触媒の内部細孔が十分に利用できなくなる傾向にある。
(Porous material shape and use as a catalyst)
The shape of the porous material having solid acidity according to the present invention is not particularly limited, but is preferably particulate or film-like for convenience as a catalyst. When the shape is particulate, the average particle diameter of the particles is preferably 0.01 to 100 μm, more preferably 0.01 to 50 μm, and particularly preferably 0.1 to 50 μm. When the average particle size of the catalyst is less than 0.01 μm, the particles are likely to be scattered and difficult to handle. On the other hand, when the average particle size exceeds 100 μm, the internal pores of the catalyst are fully utilized. It tends to be impossible.
本発明の配位高分子化合物を触媒として利用する場合は、上記粒子からなる粉末のまま使用しても良いが、必要に応じて成形して使用しても良い。成形する手段はどのようなものでも良いが、押出成形、打錠成形、転動成形、圧縮成形、ＣＩＰ等が好ましい。その形状は使用箇所、方法に応じて決めることができ、例えば円柱状、破砕状、球状、ハニカム状、凹凸状、波板状等が挙げられる。 When the coordination polymer compound of the present invention is used as a catalyst, it may be used as a powder composed of the above particles, but may be molded and used as necessary. Any molding means may be used, but extrusion molding, tablet molding, rolling molding, compression molding, CIP and the like are preferable. The shape can be determined according to the location and method of use, and examples thereof include a columnar shape, a crushed shape, a spherical shape, a honeycomb shape, an uneven shape, and a corrugated shape.
かくして製造される本発明の多孔性材料は、本発明の多孔性材料の特徴として上述のとおり耐熱性に優れ、比表面積が大きく、均一な細孔径を有し、且つ固体酸性を有する。具体的には、ＢＥＴ比表面積が８００ｍ２／ｇ以上、細孔径が均一、耐熱温度が１００℃以上で、固体酸量０．１ｍｍｏｌ／ｇ以上の固体酸性を有することを確認することにより、本発明の多孔性材料として用いられる。 As described above, the porous material of the present invention produced in this way is excellent in heat resistance, has a large specific surface area, has a uniform pore diameter, and has solid acidity as described above. Specifically, by confirming that the BET specific surface area is 800 m 2 / g or more, the pore diameter is uniform, the heat resistant temperature is 100 ° C. or more, and the solid acid amount is 0.1 mmol / g or more, the solid acidity is confirmed. Used as a porous material of the invention.
本発明の多孔性材料は、固体酸触媒として使用可能でありアルキル化、アシル化、オリゴマー化、異性化、水和、糖類などの加水分解、エーテル化、エステル化、水素化分解、有機化合物のニトロ化、ベックマン転位反応などの反応に使用でき、特に、フェノールとアセトンからビスフェノールＡ化合物を製造する際の触媒として効果的に使用される。
また、本発明の多孔性配位高分子化合物は、フリーのスルホン酸部位を有する多孔質でありＢＥＴ法による比表面積も８００ｍ２／ｇ以上と非常に大きいことから水蒸気やメタン、二酸化炭素、水素などのガス吸蔵材として、さらに乾燥剤、分別材料、分析材料、電池材料、ガスセンサーなどの用途に使用することも含まれる。
The porous material of the present invention can be used as a solid acid catalyst and can be used for alkylation, acylation, oligomerization, isomerization, hydration, hydrolysis of saccharides, etherification, esterification, hydrogenolysis, organic compounds. It can be used for reactions such as nitration and Beckmann rearrangement, and is particularly effective as a catalyst for producing bisphenol A compounds from phenol and acetone.
In addition, the porous coordination polymer compound of the present invention is porous having a free sulfonic acid moiety and has a very large specific surface area of 800 m 2 / g or more by the BET method, so that water vapor, methane, carbon dioxide, hydrogen Further, it is also included that the gas storage material such as desiccant, separation material, analysis material, battery material, gas sensor and the like is used.
以下、実施例を挙げて本発明を詳細に説明するが、本発明の範囲はこれらの実施例により限定されるものではない。
（粉末Ｘ線回折）
配位高分子化合物のＸ線回折の測定は、粉末Ｘ線回折装置を用い、ターゲットにＣｕを有するＸ線管球から発生したＸ線を試料に照射し、試料により回折された回折Ｘ線をモノクロメーターまたはＮｉフィルターにてＣｕＫα線に単色化されたものを検出することにより行なった。回折ピークの位置は、２θ（回折角）として表される。なおθはブラッグ角を示し、オングストローム単位における面間隔（ｄ値）はブラッグの条件式（２ｄｓｉｎθ＝λ）から計算される。ここでλは測定に用いたＸ線の波長を示す。ピーク位置はピークトップとして表す。また、通常、２θの測定は、人的誤差と機械的誤差との両者を受ける。以上の誤差等を考慮して、測定値の±の範囲を約プラスマイナス０．３°として規定した。
Ｘ線回折装置：ＰＡＮａｌｙｔｉｃａｌ社製 ＰＷ１７００
使用Ｘ線：ＣｕＫα線（λ＝１．５４１８４Å）
管電圧、管電流：４０ｋＶ、３０ｍＶ
発散スリット（ＤＳ）＝１．０度
散乱スリット（ＳＳ）＝１．０度
受光スリット（ＳＳ）＝０．２ｍｍ
走査方法：θ／２θスキャン
走査角度：３〜４０度
EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated in detail, the scope of the present invention is not limited by these Examples.
(Powder X-ray diffraction)
The X-ray diffraction of the coordination polymer compound is measured using a powder X-ray diffractometer, irradiating the sample with X-rays generated from an X-ray tube having Cu as a target, and diffracted X-rays diffracted by the sample This was carried out by detecting the monochromatized CuCu ray with a monochromator or Ni filter. The position of the diffraction peak is expressed as 2θ (diffraction angle). Note that θ represents the Bragg angle, and the surface interval (d value) in angstrom units is calculated from the Bragg conditional expression (2 d sin θ = λ). Here, λ represents the wavelength of the X-ray used for the measurement. The peak position is represented as the peak top. In general, the measurement of 2θ is subject to both human error and mechanical error. In consideration of the above errors and the like, the range of ± of the measured value is defined as about plus or minus 0.3 °.
X-ray diffractometer: PW1700 manufactured by PANalytical
X-ray used: CuKα ray (λ = 1.54184Å)
Tube voltage, tube current: 40 kV, 30 mV
Diverging slit (DS) = 1.0 degree Scattering slit (SS) = 1.0 degree Receiving slit (SS) = 0.2 mm
Scanning method: θ / 2θ scan Scanning angle: 3 to 40 degrees
（元素分析）
配位高分子化合物の組成分析に関しては、以下に示す方法にて実施した。クロムはアルカリ溶融し溶解した溶液をＩＣＰ発光分析装置（ＨＯＲＩＢＡ ＪＯＢＩＮ ＹＶＯＮ社製ＵＬＴＩＭＡ ２Ｃ型）を用いて波長２０５．５５２ｎｍで定量した。炭素、水素はＣＨＮ分析計（Ｐａｒｋｉｎ Ｅｌｍｅｒ社製２４００ＩＩ型）で、酸素は酸素窒素分析計（Ｌｅｃｏ社製ＴＣ−４３６型）で定量した。イオウは自動試料燃焼装置（三菱化学アナリテック社製ＡＱＦ−１００型）で燃焼し発生したガス成分を吸収した溶液をイオンクロマトグラフ分析装置（ＤＩＯＮＥＸ社製ＤＸ−５００型）で定量した。ナトリウムは湿式分解し溶解した溶液を原子吸光分析装置（ＶＡＲＩＡＮ社製ＳｐｅｃｔｒＡＡ ２２０型）で定量した。
(Elemental analysis)
The composition analysis of the coordination polymer compound was carried out by the following method. Chromium was quantified at a wavelength of 205.552 nm using an ICP emission analyzer (ULTIMA 2C type, manufactured by HORIBA JOBIN YVON) by melting in an alkali solution. Carbon and hydrogen were quantified with a CHN analyzer (Parkin Elmer type 2400II), and oxygen was quantified with an oxygen nitrogen analyzer (Leco TC-436 type). Sulfur was quantified with an ion chromatograph analyzer (DX-500 type manufactured by DIONEX) after absorbing the gas components generated by burning with an automatic sample combustion device (AQF-100 type manufactured by Mitsubishi Chemical Analytech). Sodium was quantified with an atomic absorption spectrometer (SpectrAA 220 type, manufactured by VARIAN) after dissolving it by wet decomposition.
（ＢＥＴ比表面積、細孔径分布）
細孔径分布および比表面積の測定に関しては、カンタークローム社製 全自動ガス吸着測定装置 ＡＳ−３Ｂを用いて窒素吸着により比表面積は多点法を用いて、細孔径分布はＢＪＨ法にて、解析範囲を拡張して実施した。
（固体酸量）
固体酸量は乾燥した状態の錯体 ０．５ｇを常温の飽和塩化ナトリウム水溶液に３０分に入れ、水酸化ナトリウム水溶液にて滴定し算出した。
(BET specific surface area, pore size distribution)
Regarding the measurement of the pore size distribution and specific surface area, the specific surface area is analyzed by multipoint method and the pore size distribution is analyzed by BJH method by nitrogen adsorption using AS-3B manufactured by Canterchrome. The scope was extended.
(Solid acid amount)
The amount of the solid acid was calculated by placing 0.5 g of the dried complex in a saturated sodium chloride aqueous solution at room temperature for 30 minutes and titrating with a sodium hydroxide aqueous solution.
（熱重量測定 ＴＧ）
熱重量測定は熱重量分析器（セイコー電子工業社製ＳＳＣ／５２００シリーズ）を用いて測定した。
(Thermogravimetry TG)
Thermogravimetry was performed using a thermogravimetric analyzer (SSC / 5200 series manufactured by Seiko Denshi Kogyo Co., Ltd.).
実施例１ 多孔性配位高分子合成例
１５０ｍｌテフロン（登録商標）容器に酸化クロム（VI）１．２５ｇ、２−スルホテレフタル酸ナトリウム２．０１ｇ、塩酸０．９１ｇに水５０ｍｌ加え攪拌した。これをステンレス製オートクレーブに仕込み、１８０℃で１４４時間反応させた。反応後１晩冷却し、固体をろ過して沈殿物を回収した。沈殿物を１Ｎの硫酸に１時間ほど浸した後、水―アセトンのの等量混合溶液で３回以上洗浄し、１２０℃で減圧乾燥し、緑色固体１．９ｇを得た。
Example 1 Porous Coordination Polymer Synthesis Example To a 150 ml Teflon (registered trademark) container, 1.25 g of chromium (VI) oxide, 2.01 g of sodium 2-sulfoterephthalate and 0.91 g of hydrochloric acid were added with 50 ml of water and stirred. This was put into a stainless steel autoclave and reacted at 180 ° C. for 144 hours. After the reaction, the mixture was cooled overnight, and the solid was filtered to collect a precipitate. The precipitate was immersed in 1N sulfuric acid for about 1 hour, then washed with an equal amount of water-acetone mixed solution three times or more and dried under reduced pressure at 120 ° C. to obtain 1.9 g of a green solid.
窒素吸着によるＢＥＴ比表面積は（多点法解析１３６２ｍ２／ｇ）であり、９〜２１ｎｍの細孔が全細孔容積の７０％程度であった。多点法吸着測定結果を図７に示し、細孔径分布に関して図８に示す。細孔径分布測定結果より、分布が狭く均一な細孔であることがわかった。
この配位高分子化合物を１晩飽和水蒸気を吸着させた後、Ｘ線回折測定結果を図９に示す。また元素分析による重量分析結果は表１のようになり下記の組成式（８）に示す構造であることが推定される。
The BET specific surface area by nitrogen adsorption was (multipoint analysis 1362 m 2 / g), and 9 to 21 nm pores were about 70% of the total pore volume. The multipoint method adsorption measurement results are shown in FIG. 7, and the pore size distribution is shown in FIG. From the pore size distribution measurement results, it was found that the pores were narrow and uniform.
FIG. 9 shows the result of X-ray diffraction measurement after adsorbing saturated water vapor to this coordination polymer compound overnight. Further, the results of gravimetric analysis by elemental analysis are as shown in Table 1, and it is presumed that the structure is shown in the following composition formula (8).
ＸＲＰＤ測定結果から、少なくとも３．３°±０．３°、８．４°±０．３°及び９．０°±０．３°の回折角（２θ）に回折ピークを有することが分かった。また、この配位高分子化合物の熱重量測定した結果を図１０に示す。また乾燥錯体０．５ｇを飽和塩化ナトリウム水溶液に入れ、水溶液中の塩酸量を滴定した結果１．０ｍｍｏｌ／ｇであった。以下この錯体をクロム−２スルホテレフタル酸錯体と略記する。 From XRPD measurement results, it was found that there were diffraction peaks at diffraction angles (2θ) of at least 3.3 ° ± 0.3 °, 8.4 ° ± 0.3 °, and 9.0 ° ± 0.3 °. . Further, the results of thermogravimetric measurement of this coordination polymer compound are shown in FIG. Further, 0.5 g of the dried complex was put into a saturated aqueous sodium chloride solution, and the amount of hydrochloric acid in the aqueous solution was titrated, resulting in 1.0 mmol / g. Hereinafter, this complex is abbreviated as a chromium-2 sulfoterephthalic acid complex.
実施例２ エステル化反応
５０ｍｌ反応容器中に、メタノール溶媒中（３０ｃｃ）にヘキサン酸０．３３ｇを入れ、触媒として実施例１で合成したクロム−２スルホテレフタル酸錯体０．４５ｇを加え、加熱還流を６時間実施しエステル化を実施した。生成したエステルの同定はガスクロマトグラフィー（ＧＣ）により行った。測定の結果ヘキサン酸メチルへの転化率は８０％であった。
In Example 2 esterification 50ml reaction vessel, placed hexanoic acid 0.33g in methanol solvent (30 cc), chromium -2 sulfoterephthalic acid complex 0.45g synthesized in Example 1 as a catalyst was added, heated to reflux For 6 hours to carry out esterification. The resulting ester was identified by gas chromatography (GC). As a result of the measurement, the conversion rate to methyl hexanoate was 80%.
実施例３ ビスフェノールＡ製造反応
５０ｍｌ反応容器中に、フェノール溶媒９．０ｇに触媒として実施例１で合成したクロム−２スルホテレフタル酸錯体０．５２ｇを加え、助触媒として４−アミノエタンチオールを酸量に対して３０％相当０．０３０ｇ加え７０℃で１時間 攪拌、加熱を行なった。反応後、アセトン０．４４５２ｇを滴下し、１１０℃に昇温、攪拌し１時間ＢＰＡ合成反応を実施した。減少していくアセトンの定量はガスクロマトグラフィー（ＧＣ）により行い、生成したＢＰＡの定量は液体クロマトグラフィー（ＬＣ）により行なった。反応１時間後のアセトン転化率は８１．７％であり、ＢＰＡ収率は５４．１％であった。
Example 3 Bisphenol A Production Reaction In a 50 ml reaction vessel, 0.52 g of the chromium-2 sulfoterephthalic acid complex synthesized in Example 1 was added as a catalyst to 9.0 g of a phenol solvent, and 4-aminoethanethiol was acid as a cocatalyst. 0.030 g corresponding to 30% of the amount was added, and the mixture was stirred and heated at 70 ° C. for 1 hour. After the reaction, 0.4452 g of acetone was added dropwise, the temperature was raised to 110 ° C. and stirred, and a BPA synthesis reaction was carried out for 1 hour. Acetone declining was quantified by gas chromatography (GC), and the produced BPA was quantified by liquid chromatography (LC). The acetone conversion after 1 hour of reaction was 81.7%, and the BPA yield was 54.1%.
比較例１ クロム−テレフタル酸触媒を用いたエステル化反応
５０ｍｌ反応容器中に、メタノール溶媒３０ｃｃ、ヘキサン酸０．３３ｇを入れ、触媒として非特許文献１に示される錯体０．４５ｇを加え、加熱還流を６時間実施しエステル化を実施した。生成したエステルの同定は実施例１同様ガスクロマトグラフィー（ＧＣ）により行った。測定の結果ヘキサン酸メチルへの転化率は２％であった。
Comparative Example 1 In a 50 ml reaction vessel using a chromium-terephthalic acid catalyst, 30 cc of methanol solvent and 0.33 g of hexanoic acid were added, and 0.45 g of the complex shown in Non-Patent Document 1 was added as a catalyst, followed by heating to reflux. For 6 hours to carry out esterification. The produced ester was identified by gas chromatography (GC) as in Example 1. As a result of the measurement, the conversion rate to methyl hexanoate was 2%.
比較例２ イオン交換樹脂を触媒として用いたビスフェノールＡ製造反応
５０ｍｌ反応容器中に、フェノール溶媒９．０ｇに触媒としてイオン交換樹脂を実施例３の酸量と同量０．３ｇ加え、助触媒として４−アミノエタンチオールを酸量に対して３０％相当０．０３０ｇ加え７０℃で１時間 攪拌、加熱を行なった。
アセトン０．４４５２ｇを滴下し、１１０℃に昇温、攪拌し１時間ＢＰＡ合成反応を実施した。減少していくアセトンの定量はガスクロマトグラフィー（ＧＣ）により行い、生成したＢＰＡの定量は液体クロマトグラフィー（ＬＣ）により行なった。反応１時間後のアセトン転化率は６１．３％であり、ＢＰＡ収率は ５１．３％であった。
Comparative Example 2 In a 50 ml reaction vessel for producing bisphenol A using an ion exchange resin as a catalyst, 0.3 g of the ion exchange resin as an acid amount in Example 3 was added to 9.0 g of a phenol solvent as a catalyst. 0.030 g corresponding to 30% of 4-aminoethanethiol was added to the acid amount, and the mixture was stirred and heated at 70 ° C. for 1 hour.
0.4452 g of acetone was added dropwise, the temperature was raised to 110 ° C. and stirred, and a BPA synthesis reaction was carried out for 1 hour. Acetone declining was quantified by gas chromatography (GC), and the produced BPA was quantified by liquid chromatography (LC). The acetone conversion after 1 hour of the reaction was 61.3%, and the BPA yield was 51.3%.
Claims (8)
｛Ｍ１（ＯＯＣ−Ｒ−ＣＯＯ）｝２ ・・・（１）
（式中、Ｍ１はＣｕ２＋、Ｒｈ２＋、Ｚｎ２＋、Ｍｏ２＋、Ｃｒ２＋、Ｃｏ２＋から選択される２価の金属イオンを表わす。Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表わし、他の置換基により置換されていてもよい。）
｛Ｍ２ ３Ｏ（ＯＯＣ−Ｒ−ＣＯＯ）３｝ ・・・（２）
（式中、Ｍ２はＣｒ３＋、Ｒｕ３＋、Ｆｅ３＋、Ｍｎ３＋、Ｖ３＋、Ｔｉ３＋、Ｃｏ３＋から選択される３価の金属イオンを表わす。Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表わし、他の置換基により置換されていてもよい。）
｛Ｚｎ４Ｏ（ＯＯＣ−Ｒ−ＣＯＯ）３｝ ・・・（３）
（式中、Ｒは１つ以上のスルホン酸基を有する芳香族化合物を表し、他の置換基により置換されていてもよい。） The structural unit of the coordination polymer compound is a binuclear metal cluster represented by the general formula (1), a trinuclear metal cluster represented by the general formula (2), or a tetranuclear metal cluster represented by the general formula (3). The porous material according to claim 2, comprising any one of the ligands having two or more carboxylic acids and one or more sulfonic acid groups.
{M 1 (OOC-R-COO)} 2 (1)
(In the formula, M 1 represents a divalent metal ion selected from Cu 2+ , Rh 2+ , Zn 2+ , Mo 2+ , Cr 2+ , and Co 2+. R represents an aromatic compound having one or more sulfonic acid groups. And may be substituted with other substituents.)
{M 2 3 O (OOC-R-COO) 3 } (2)
(In the formula, M 2 represents a trivalent metal ion selected from Cr 3+ , Ru 3+ , Fe 3+ , Mn 3+ , V 3+ , Ti 3+ , and Co 3+. R has one or more sulfonic acid groups. Represents an aromatic compound and may be substituted with other substituents.)
{Zn 4 O (OOC—R—COO) 3 } (3)
(In the formula, R represents an aromatic compound having one or more sulfonic acid groups, and may be substituted with other substituents.)
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| JP2012250946A (en) * | 2011-06-06 | 2012-12-20 | Shoei Chem Ind Co | Method for producing porous metal complex |
| JP2014533230A (en) * | 2011-08-16 | 2014-12-11 | コリア リサーチ インスティテュート オブ ケミカル テクノロジー | Composite comprising crystalline hybrid nanoporous powder and method for producing the same |
| CN104324754A (en) * | 2014-10-13 | 2015-02-04 | 大连理工大学 | Preparation method and application of bimetallic photocatalytic functional POM/MOFs |
| JP2015117202A (en) * | 2013-12-18 | 2015-06-25 | 新日鐵住金株式会社 | Coordination polymer complex containing fluorine, gas adsorbent, gas separation apparatus and gas storage apparatus using the same |
| WO2015170688A1 (en) * | 2014-05-07 | 2015-11-12 | 国立大学法人北陸先端科学技術大学院大学 | Metal-supported porous coordination polymer catalyst |
| CN115403493A (en) * | 2021-05-26 | 2022-11-29 | 中国石油化工股份有限公司 | Metal organic framework material with sulfonyl benzene ring structure, preparation method and application thereof, and carboxylic acid esterification method |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012250946A (en) * | 2011-06-06 | 2012-12-20 | Shoei Chem Ind Co | Method for producing porous metal complex |
| JP2014533230A (en) * | 2011-08-16 | 2014-12-11 | コリア リサーチ インスティテュート オブ ケミカル テクノロジー | Composite comprising crystalline hybrid nanoporous powder and method for producing the same |
| JP2015117202A (en) * | 2013-12-18 | 2015-06-25 | 新日鐵住金株式会社 | Coordination polymer complex containing fluorine, gas adsorbent, gas separation apparatus and gas storage apparatus using the same |
| WO2015170688A1 (en) * | 2014-05-07 | 2015-11-12 | 国立大学法人北陸先端科学技術大学院大学 | Metal-supported porous coordination polymer catalyst |
| CN104324754A (en) * | 2014-10-13 | 2015-02-04 | 大连理工大学 | Preparation method and application of bimetallic photocatalytic functional POM/MOFs |
| CN115403493A (en) * | 2021-05-26 | 2022-11-29 | 中国石油化工股份有限公司 | Metal organic framework material with sulfonyl benzene ring structure, preparation method and application thereof, and carboxylic acid esterification method |
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