JP2018505550A5 - - Google Patents

Info

Publication number

JP2018505550A5

JP2018505550A5 JP2017534979A JP2017534979A JP2018505550A5 JP 2018505550 A5 JP2018505550 A5 JP 2018505550A5 JP 2017534979 A JP2017534979 A JP 2017534979A JP 2017534979 A JP2017534979 A JP 2017534979A JP 2018505550 A5 JP2018505550 A5 JP 2018505550A5

Authority

JP

Japan

Prior art keywords

group

electroluminescent device

charged

metal

formula

Prior art date

2015-12-29

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
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• 230000003111 delayed effect Effects 0.000 claims 18
• -1 cyclopentane-1,3-diyl Chemical group 0.000 claims 17
• 125000005647 linker group Chemical group 0.000 claims 17
• 125000003118 aryl group Chemical group 0.000 claims 13
• 239000002184 metal Substances 0.000 claims 9
• 125000001072 heteroaryl group Chemical group 0.000 claims 8
• 150000002500 ions Chemical class 0.000 claims 8
• 125000000217 alkyl group Chemical group 0.000 claims 7
• 150000001875 compounds Chemical class 0.000 claims 7
• 125000002252 acyl group Chemical group 0.000 claims 6
• 125000003545 alkoxy group Chemical group 0.000 claims 6
• 125000004414 alkyl thio group Chemical group 0.000 claims 6
• 150000001408 amides Chemical class 0.000 claims 6
• 125000004122 cyclic group Chemical group 0.000 claims 6
• 150000002148 esters Chemical class 0.000 claims 6
• 125000005843 halogen group Chemical group 0.000 claims 6
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 6
• 229940124530 sulfonamide Drugs 0.000 claims 6
• 150000003456 sulfonamides Chemical class 0.000 claims 6
• 125000003441 thioacyl group Chemical group 0.000 claims 6
• 125000000743 hydrocarbylene group Chemical group 0.000 claims 5
• 239000000463 material Substances 0.000 claims 4
• 238000000034 method Methods 0.000 claims 4
• KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 3
• 150000004657 carbamic acid derivatives Chemical class 0.000 claims 3
• OKQKDCXVLPGWPO-UHFFFAOYSA-N sulfanylidenephosphane Chemical compound S=P OKQKDCXVLPGWPO-UHFFFAOYSA-N 0.000 claims 3
• 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 2
• 150000004820 halides Chemical class 0.000 claims 2
• 239000000203 mixture Substances 0.000 claims 2
• 125000000962 organic group Chemical group 0.000 claims 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
• 125000001424 substituent group Chemical group 0.000 claims 2
• 125000003107 substituted aryl group Chemical group 0.000 claims 2
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
• MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 claims 2
• 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims 1
• QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
• XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
• ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
• 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims 1
• 150000007942 carboxylates Chemical class 0.000 claims 1
• 150000001768 cations Chemical class 0.000 claims 1
• 238000005401 electroluminescence Methods 0.000 claims 1
• 229910052736 halogen Inorganic materials 0.000 claims 1
• 150000002367 halogens Chemical class 0.000 claims 1
• ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 1
• DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical compound [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 claims 1
• 239000002608 ionic liquid Substances 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 229910052755 nonmetal Inorganic materials 0.000 claims 1
• AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 1
• 230000000737 periodic effect Effects 0.000 claims 1
• UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 1
• XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical group [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 1
• 125000002743 phosphorus functional group Chemical group 0.000 claims 1
• 229920006395 saturated elastomer Polymers 0.000 claims 1
• BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
• 0 *c1c(c(c(*)c(*)c(*)c2*)c2[n]2-c(c(*)c(c(C#N)c3*)C#N)c3-[n](c3c(*)c(*)c(*)c(*)c33)c4c3c(*)c(*)c(*)c4*)c2c(*)c(*)c1* Chemical compound *c1c(c(c(*)c(*)c(*)c2*)c2[n]2-c(c(*)c(c(C#N)c3*)C#N)c3-[n](c3c(*)c(*)c(*)c(*)c33)c4c3c(*)c(*)c(*)c4*)c2c(*)c(*)c1* 0.000 description 3
• QOFNOQMBQWXQHI-UHFFFAOYSA-N OC(c(c(C(O)=O)c1)cc(-[n]2c3ccccc3c3c2cccc3)c1-[n]1c(cccc2)c2c2c1cccc2)=O Chemical compound OC(c(c(C(O)=O)c1)cc(-[n]2c3ccccc3c3c2cccc3)c1-[n]1c(cccc2)c2c2c1cccc2)=O QOFNOQMBQWXQHI-UHFFFAOYSA-N 0.000 description 1