JP7176796B2 - N,n’-ジアリール尿素誘導体及びそれを用いた感熱記録材料 - Google Patents
N,n’-ジアリール尿素誘導体及びそれを用いた感熱記録材料 Download PDFInfo
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- JP7176796B2 JP7176796B2 JP2021515971A JP2021515971A JP7176796B2 JP 7176796 B2 JP7176796 B2 JP 7176796B2 JP 2021515971 A JP2021515971 A JP 2021515971A JP 2021515971 A JP2021515971 A JP 2021515971A JP 7176796 B2 JP7176796 B2 JP 7176796B2
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- bis
- phenyloxysulfonyl
- benzene
- ureido
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- 239000000463 material Substances 0.000 title claims description 52
- -1 monocyclic aromatic hydrocarbon Chemical class 0.000 claims description 109
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
- 125000000962 organic group Chemical group 0.000 claims description 37
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 18
- 125000005647 linker group Chemical group 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000000981 basic dye Substances 0.000 claims description 10
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 9
- 239000000975 dye Substances 0.000 claims description 9
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 6
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims description 3
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 3
- 125000005163 aryl sulfanyl group Chemical group 0.000 claims description 3
- 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims description 3
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 3
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
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- 238000012360 testing method Methods 0.000 description 33
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- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 14
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- WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 8
- PQALGAIRWUHQRQ-UHFFFAOYSA-N 1-(3-hydroxyphenyl)-3-(3-methylphenyl)urea Chemical compound CC1=CC=CC(NC(=O)NC=2C=C(O)C=CC=2)=C1 PQALGAIRWUHQRQ-UHFFFAOYSA-N 0.000 description 7
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 7
- 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 7
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
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- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 230000035945 sensitivity Effects 0.000 description 7
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- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 229920002472 Starch Polymers 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000001023 inorganic pigment Substances 0.000 description 6
- 229920000126 latex Polymers 0.000 description 6
- 239000004816 latex Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 235000019698 starch Nutrition 0.000 description 6
- YYUJEEGDLCZLSE-UHFFFAOYSA-N 1-(3-hydroxyphenyl)-3-phenylurea Chemical compound OC1=CC=CC(NC(=O)NC=2C=CC=CC=2)=C1 YYUJEEGDLCZLSE-UHFFFAOYSA-N 0.000 description 5
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical compound C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 5
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- 239000004215 Carbon black (E152) Substances 0.000 description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 5
- 235000012211 aluminium silicate Nutrition 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
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- 239000011241 protective layer Substances 0.000 description 5
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- WGRXEVDJFKLCSI-UHFFFAOYSA-N CC1=CC(=CC=C1)NC(=O)NC2=CC(=CC=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=CC(=C4)NC(=O)NC5=CC=CC(=C5)C Chemical compound CC1=CC(=CC=C1)NC(=O)NC2=CC(=CC=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=CC(=C4)NC(=O)NC5=CC=CC(=C5)C WGRXEVDJFKLCSI-UHFFFAOYSA-N 0.000 description 4
- HDNWLHQUIKUVLH-UHFFFAOYSA-N CC1=CC(=CC=C1)NC(=O)NC2=CC=C(C=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=C(C=C4)NC(=O)NC5=CC=CC(=C5)C Chemical compound CC1=CC(=CC=C1)NC(=O)NC2=CC=C(C=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=C(C=C4)NC(=O)NC5=CC=CC(=C5)C HDNWLHQUIKUVLH-UHFFFAOYSA-N 0.000 description 4
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
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- BGLZECVIKIGPIF-UHFFFAOYSA-N 1-[2-(benzenesulfonamido)phenyl]-3-phenylurea Chemical compound C=1C=CC=C(NS(=O)(=O)C=2C=CC=CC=2)C=1NC(=O)NC1=CC=CC=C1 BGLZECVIKIGPIF-UHFFFAOYSA-N 0.000 description 3
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- PPSHVOHSIJJBGJ-UHFFFAOYSA-N bis[3-[(4-tert-butylphenyl)carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CC(C)(C)C1=CC=C(C=C1)NC(=O)NC2=CC(=CC=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=CC(=C4)NC(=O)NC5=CC=C(C=C5)C(C)(C)C PPSHVOHSIJJBGJ-UHFFFAOYSA-N 0.000 description 1
- UNPHSWZGFOYBJR-UHFFFAOYSA-N bis[3-[[2-methyl-5-(phenoxycarbonylamino)phenyl]carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CC1=C(C=C(C=C1)NC(=O)OC2=CC=CC=C2)NC(=O)NC3=CC(=CC=C3)OS(=O)(=O)C4=CC(=CC=C4)S(=O)(=O)OC5=CC=CC(=C5)NC(=O)NC6=C(C=CC(=C6)NC(=O)OC7=CC=CC=C7)C UNPHSWZGFOYBJR-UHFFFAOYSA-N 0.000 description 1
- HXDIECHJANVNDM-UHFFFAOYSA-N bis[3-[[2-methyl-5-[(4-methylphenoxy)carbonylamino]phenyl]carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CC1=CC=C(C=C1)OC(=O)NC2=CC(=C(C=C2)C)NC(=O)NC3=CC(=CC=C3)OS(=O)(=O)C4=CC(=CC=C4)S(=O)(=O)OC5=CC=CC(=C5)NC(=O)NC6=C(C=CC(=C6)NC(=O)OC7=CC=C(C=C7)C)C HXDIECHJANVNDM-UHFFFAOYSA-N 0.000 description 1
- SGRVOAOYSUIATK-UHFFFAOYSA-N bis[3-[[4-(benzenesulfonamido)phenyl]carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound C1=CC=C(C=C1)S(=O)(=O)NC2=CC=C(C=C2)NC(=O)NC3=CC(=CC=C3)OS(=O)(=O)C4=CC(=CC=C4)S(=O)(=O)OC5=CC=CC(=C5)NC(=O)NC6=CC=C(C=C6)NS(=O)(=O)C7=CC=CC=C7 SGRVOAOYSUIATK-UHFFFAOYSA-N 0.000 description 1
- UQFZBSASABVXOG-UHFFFAOYSA-N bis[3-[[4-(benzenesulfonyl)phenyl]carbamoylamino]phenyl] benzene-1,2-disulfonate Chemical compound C1=CC=C(C=C1)S(=O)(=O)C2=CC=C(C=C2)NC(=O)NC3=CC(=CC=C3)OS(=O)(=O)C4=CC=CC=C4S(=O)(=O)OC5=CC=CC(=C5)NC(=O)NC6=CC=C(C=C6)S(=O)(=O)C7=CC=CC=C7 UQFZBSASABVXOG-UHFFFAOYSA-N 0.000 description 1
- OFENRRHDURBIJH-UHFFFAOYSA-N bis[3-[[4-(benzenesulfonyl)phenyl]carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound C1=CC=C(C=C1)S(=O)(=O)C2=CC=C(C=C2)NC(=O)NC3=CC(=CC=C3)OS(=O)(=O)C4=CC(=CC=C4)S(=O)(=O)OC5=CC=CC(=C5)NC(=O)NC6=CC=C(C=C6)S(=O)(=O)C7=CC=CC=C7 OFENRRHDURBIJH-UHFFFAOYSA-N 0.000 description 1
- WGGMYDMWTDIUBS-UHFFFAOYSA-N bis[4-[(4-acetamidophenyl)carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CC(=O)NC1=CC=C(C=C1)NC(=O)NC2=CC=C(C=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=C(C=C4)NC(=O)NC5=CC=C(C=C5)NC(=O)C WGGMYDMWTDIUBS-UHFFFAOYSA-N 0.000 description 1
- TUFRDIYOJUUNMC-UHFFFAOYSA-N bis[4-[(4-benzoylphenyl)carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)NC(=O)NC3=CC=C(C=C3)OS(=O)(=O)C4=CC(=CC=C4)S(=O)(=O)OC5=CC=C(C=C5)NC(=O)NC6=CC=C(C=C6)C(=O)C7=CC=CC=C7 TUFRDIYOJUUNMC-UHFFFAOYSA-N 0.000 description 1
- MVDPGXKITCRDJN-UHFFFAOYSA-N bis[4-[(4-ethylsulfonylphenyl)carbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CCS(=O)(=O)C1=CC=C(C=C1)NC(=O)NC2=CC=C(C=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=C(C=C4)NC(=O)NC5=CC=C(C=C5)S(=O)(=O)CC MVDPGXKITCRDJN-UHFFFAOYSA-N 0.000 description 1
- JAFNRBRYUHWHKI-UHFFFAOYSA-N bis[4-[(4-methylphenyl)methylcarbamoylamino]phenyl] benzene-1,3-disulfonate Chemical compound CC1=CC=C(C=C1)CNC(=O)NC2=CC=C(C=C2)OS(=O)(=O)C3=CC(=CC=C3)S(=O)(=O)OC4=CC=C(C=C4)NC(=O)NCC5=CC=C(C=C5)C JAFNRBRYUHWHKI-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- VZHRPLJULARYDO-UHFFFAOYSA-N butane-1,4-disulfonyl chloride Chemical compound ClS(=O)(=O)CCCCS(Cl)(=O)=O VZHRPLJULARYDO-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 125000006630 butoxycarbonylamino group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical compound C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000011981 development test Methods 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000000598 endocrine disruptor Substances 0.000 description 1
- 231100000049 endocrine disruptor Toxicity 0.000 description 1
- VRHMNTYGRQBMGR-UHFFFAOYSA-N ethane-1,2-disulfonyl chloride Chemical compound ClS(=O)(=O)CCS(Cl)(=O)=O VRHMNTYGRQBMGR-UHFFFAOYSA-N 0.000 description 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 125000006626 methoxycarbonylamino group Chemical group 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 230000007886 mutagenicity Effects 0.000 description 1
- 231100000299 mutagenicity Toxicity 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JTHNLKXLWOXOQK-UHFFFAOYSA-N n-propyl vinyl ketone Natural products CCCC(=O)C=C JTHNLKXLWOXOQK-UHFFFAOYSA-N 0.000 description 1
- BCXWMIMRDMIJGL-UHFFFAOYSA-N naphthalene-1,5-disulfonyl chloride Chemical compound C1=CC=C2C(S(=O)(=O)Cl)=CC=CC2=C1S(Cl)(=O)=O BCXWMIMRDMIJGL-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- LPJOPBVGMAXNQS-UHFFFAOYSA-N phenyl N-[3-[2-[2,3-bis[N-(methylcarbamoyl)-3-(phenoxycarbonylamino)anilino]phenyl]sulfonyl-N-(methylcarbamoyl)-6-[N-(methylcarbamoyl)-3-(phenoxycarbonylamino)anilino]anilino]phenyl]carbamate Chemical compound CNC(=O)N(C1=C(C(=CC=C1)S(=O)(=O)C2=CC=CC(=C2N(C3=CC=CC(=C3)NC(=O)OC4=CC=CC=C4)C(=O)NC)N(C5=CC=CC(=C5)NC(=O)OC6=CC=CC=C6)C(=O)NC)N(C7=CC=CC(=C7)NC(=O)OC8=CC=CC=C8)C(=O)NC)C9=CC=CC(=C9)NC(=O)OC1=CC=CC=C1 LPJOPBVGMAXNQS-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 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
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
- 125000006410 propenylene group Chemical group 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 238000013112 stability test Methods 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/30—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used using chemical colour formers
- B41M5/333—Colour developing components therefor, e.g. acidic compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/75—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing singly-bound oxygen atoms bound to the carbon skeleton
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
更に近年は4,4’-イソプロピリデンジフェノ-ルや4,4’-ビスフェノ-ルスルホンなどは、環境ホルモンや変異原性などの環境衛生上の問題が指摘されているため、これらの問題のない非フェノ-ル系顕色剤が求められているのが実情である。
[1]下記一般式(1)で表されるN,N’-ジアリール尿素誘導体。
Rは、C1~C12のアルキル基、C2~C12のアルケニル基、C3~C12のアルキルオキシアルキル基、C3~C12のポリオキシアルキレンアルキル基、C7~C12のアラルキル基、C6~C14のアリール基、C1~C12のアルキルスルファニル基、C7~C12のアラルキルスルファニル基、C6~C14のアリールスルファニル基、C1~C12のアルキルスルホニル基、C7~C12のアラルキルスルホニル基、C6~C15のアリールスルホニル基、C7~C12のアラルキルスルホニルアミノ基、C6~C15のアリールスルホニルアミノ基、C2~C10のアシル基、C2~C10のアシルアミノ基、(C2~C10のアシル)オキシカルボニルアミノ基、(C1~C12のアルキル)オキシカルボニルアミノ基、(C7~C12のアラルキル)オキシカルボニルアミノ基、又は、(C6~C15のアリール)オキシカルボニルアミノ基を表し、隣接する2つのRは互いに結合してそれぞれが結合している炭素原子とともに芳香環または非芳香環を形成してもよい。
A,Bは、メチル基を表す。
a,b,cは、独立して、0~4の整数であり、nは0又は1である。ただし、a+cは、0~5の整数である。)
[5]式(1)、(1-1)、(2)、(3)、(4)または(5)中のZは、単環芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基、単結合で連結された複数の芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基、または、ヘテロ元素を含む連結基で連結された複数の芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基である、前記[4]に記載のN,N’-ジアリール誘導体。
[6]常温で無色ないし淡色の塩基性染料と、加熱により該染料と接触して呈色し得る顕色剤とを含有する感熱記録層を支持体上に設けた感熱記録材料であって、顕色剤として、前記[1]~[5]のいずれか一つに記載のN,N’-ジアリール尿素誘導体を含有する感熱記録材料。
本発明のN,N’-ジアリール尿素誘導体は、前記一般式(1)で表される。また、本発明のN,N’-ジアリール尿素誘導体は、前記一般式(2)~(5)で表されるものであってもよい。
また、隣接する2つのRは互いに結合してそれぞれのRが結合している炭素原子とともに芳香環を形成する場合には、好ましくは、Rが結合している芳香環とともにナフタレン環が形成される。
4,4’-ビス(3-[3-ベンジルウレイド]フェニルオキシスルホニル)ビフェニル,4,4’-ビス(3-[3-フェニルウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{p-トリル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ビフェニル、4、4’-ビス(3-[3-{p-イソプロピルフェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{p-プロペニルフェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{4-ベンゾイルフェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{4-(ベンゾイルアミノ)フェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{4-(p-トルエンスルホニル)フェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{4-(p-トルエンスルホニルアミノ)フェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、4,4’-ビス(3-[3-{4-(フェノキシカルボニルアミノ)フェニル}ウレイド]フェニルオキシスルホニル)ビフェニル、
1,3-ビス-(2-[3-{p-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{o-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{p-エチルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{p-イソプロピルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{p-tert-ブチルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{2,4,6-トリメチルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{4-アセチルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{4-ベンゾイルフェニル}ウレイレン]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{4-アセチルアミノフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{4-ベンゼンスルホニルフェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、1,3-ビス-(2-[3-{4-(フェノキシカルボニルアミノ)フェニル}ウレイド]フェニルオキシスルホニル)ベンゼン、などが挙げられる。
本発明の一般式(1)で表されるN,N’-ジアリール尿素誘導体は、下記式(7)で表される尿素化合物と下記式(8)で表されるジハロゲン化スルホニル化合物を塩基の存在下に反応させることによって容易に得ることができる。
本発明の感熱記録材料は、常温で無色ないし淡色の塩基性染料と、加熱により該塩基性染料と接触して呈色し得る顕色剤とを含有する感熱記録層を支持体上に設けた感熱記録材料であって、前記顕色剤が、前記のN,N’-ジアリール尿素誘導体を含有する。顕色剤として2種以上の化合物を併用して用いてもよく、既存の顕色剤を併用して用いてもよい。
このように微分散された分散液に、必要により顔料、バインダー、助剤等を混合撹拌することで感熱記録層塗料は調製される。
下塗り層の組成は、目的により適宜選択すればよいが、一般に、バインダー、顔料などが含まれる。
保護層に用いられるバインダ-、顔料、助剤としては、上記の感熱記録層で用いられるものが使用される。
1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼンの合成
1,3-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ベンゼンの合成
1,3-ビス-(4-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ベンゼンの合成
4,4’-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ビフェニルの合成
4,4’-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ジフェニルエ-テルの合成
4,4’-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ジフェニルエ-テルの合成
4,4’-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ビフェニルの合成
1,3-ビス-(3-[3-{p-トリル}ウレイド]フェニルオキシスルホニル)ベンゼンの合成
1,3-ビス-(3-[3-{1-ナフチル}ウレイド]フェニルオキシスルホニル)ベンゼンの合成
プラスチック中空粒子(商品名:ローペイクSN-1055:中空率:55%、固形分26.5%)100部、焼成カオリンの50%分散液100部、スチレン-ブタジエン系ラテックス(商品名:L-1571 固形分48%)25部、酸化澱粉の10%水溶液50部および水20部を混合して、アンダーコート用塗料を作成した。
[感熱記録用塗料の作成]
A液(染料分散液の調製)
3-(N,N-ジブチルアミノ)-6-メチル-7-アニリノフルオラン
10部
10%ポリビニルアルコ-ル水溶液 10部
水 16.7部
1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1) 20部
10%ポリビニルアルコ-ル水溶液 20部
水 33.3部
1,2-ビス(m-トリルオキシ)エタン 15部
10%ポリビニルアルコ-ル水溶液 15部
水 25部
A液(染料剤分散液) 36.7部
B液(顕色剤分散液) 73.3部
C液(増感剤分散液) 55.0部
支持体として坪量が53gの上質紙(酸性紙)にアンダーコート用塗料を乾燥後の面積当たりの質量が6g/m2となるように塗布および乾燥し、その後、感熱記録層用塗料を、乾燥後の面積当たりの質量が3.8g/m2になるように塗布乾燥した。
このシ-トをス-パ-カレンダ-で平滑度(JISP8155:2010)が900~1200sになるように処理して感熱記録材料を作成した。
1.感熱記録性試験(発色試験)
作成した感熱記録材料について、感熱記録紙印字試験機(大倉電気社製TH-PMD)を用い、印加エネルギー0.38mJ/dotで印加した。記録部の印字濃度はマクベス反射濃度計RD-914で測定した。これを試験前サンプル(ブランク)とした。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料を試験温度40℃、90%RHの環境下に24時間放置した後、試験片の印字部画像濃度と未印字部の濃度をマクベス反射濃度計で測定した。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料を試験温度60℃の恒温環境下に24時間放置した後、試験片の印字部画像濃度と未印字部の濃度をマクベス反射濃度計で測定した。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料を5000Luxに100時間暴露しその後、画像濃度をマクベス反射濃度計で測定した。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料を水中に15時間浸漬しその後、試験片を風乾させ、画像濃度と未印字部をマクベス反射濃度計で測定した。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料にサラダオイル中に10分間浸漬しその後、試験片の油をふき取り、画像濃度をマクベス反射濃度計で測定した。
感熱記録性試験で印加エネルギー0.38mJ/dotで記録した感熱記録材料にサラダオイル中に3時間浸漬しその後、試験片の油をふき取り、画像濃度をマクベス反射濃度計で測定した。この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を1,3-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン(合成例2)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を1,3-ビス-(4-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン(合成例3)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ビフェニル(合成例4)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-ビス-(3-[3-{m-トリル}ウレイド]フェニルオキシスルホニル)ジフェニルエ-テル(合成例5)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ジフェニルエ-テル(合成例6)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ビフェニル(合成例7)に代える以外は実施例1と同様の操作をおこなった。
この実施例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を1,3-ビス-(3-[3-{p-トリル}ウレイド]フェニルオキシスルホニル)ベンゼン(合成例8)に代える以外は実施例1と同様の操作をおこなった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を1,3-ビス-(3-[3-{1-ナフチル}ウレイド]フェニルオキシスルホニル)ベンゼン(合成例9)に代える以外は実施例1と同様の操作をおこなった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-イソプロピリデンジフェノ-ル(ビスフェノ-ルA)に代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4,4’-ジヒドロキシジフェニルスルホン(ビスフェノ-ルS)に代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4-アリルオキシ-4’-ヒドロキシジフェニルスルホンに代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)を4-ヒドロキシ-4’-イソプロピルオキシ-ジフェニルスルホンに代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)をN-3-(p-トルエンスルホニルオキシ)フェニル-N’-(p-トルエンスルホニル)-尿素に代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
実施例1のB液の1,3-ビス-(3-[3-フェニルウレイド]フェニルオキシスルホニル)ベンゼン(合成例1)をN-(2-(3-フェニルウレイド)フェニル)-ベンゼンスルホンアミドに代える以外は実施例1と同様の操作をおこなった。この参照例による感熱記録材料の各種試験結果は、表1に記載の通りであった。
Claims (5)
- 下記一般式(1)で表されるN,N’-ジアリール尿素誘導体。
Rは、C1~C12のアルキル基、C2~C12のアルケニル基、C3~C12のアルキルオキシアルキル基、C3~C12のポリオキシアルキレンアルキル基、C7~C12のアラルキル基、C6~C14のアリール基、C1~C12のアルキルスルファニル基、C7~C12のアラルキルスルファニル基、C6~C14のアリールスルファニル基、C1~C12のアルキルスルホニル基、C7~C12のアラルキルスルホニル基、C6~C15のアリールスルホニル基、C7~C12のアラルキルスルホニルアミノ基、C6~C15のアリールスルホニルアミノ基、C2~C10のアシル基、C2~C10のアシルアミノ基、(C2~C10のアシル)オキシカルボニルアミノ基、(C1~C12のアルキル)オキシカルボニルアミノ基、(C7~C12のアラルキル)オキシカルボニルアミノ基、又は、(C6~C15のアリール)オキシカルボニルアミノ基を表し、隣接する2つのRは互いに結合してそれぞれが結合している炭素原子とともに芳香環または非芳香環を形成してもよい。
A,Bは、メチル基を表す。
a,b,cは、独立して、0~4の整数であり、nは0又は1である。ただし、a+cは、0~5の整数である。) - Zは、単環芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基、単結合で連結された複数の芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基、または、ヘテロ元素を含む連結基で連結された複数の芳香族炭化水素から2個の水素原子を取り除いてできる2価の有機基である、請求項1~3のいずれか一項に記載のN,N’-ジアリール誘導体。
- 常温で無色ないし淡色の塩基性染料と、加熱により該染料と接触して呈色し得る顕色剤とを含有する感熱記録層を支持体上に設けた感熱記録材料であって、顕色剤として、請求項1~4のいずれか一項に記載のN,N’-ジアリール尿素誘導体を含有する感熱記録材料。
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