JPS5734102A - Polymer, polymerization initiator and production thereof - Google Patents

Info

Publication number

JPS5734102A

JPS5734102A JP10822080A JP10822080A JPS5734102A JP S5734102 A JPS5734102 A JP S5734102A JP 10822080 A JP10822080 A JP 10822080A JP 10822080 A JP10822080 A JP 10822080A JP S5734102 A JPS5734102 A JP S5734102A

Authority

JP

Japan

Prior art keywords

formula

polymerization initiator

compound

hydrogen

polymer

Prior art date

1980-08-08

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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• 229920000642 polymer Polymers 0.000 title abstract 2
• 239000003505 polymerization initiator Substances 0.000 title abstract 2
• 125000000524 functional group Chemical group 0.000 abstract 2
• 229910052739 hydrogen Inorganic materials 0.000 abstract 2
• 239000001257 hydrogen Substances 0.000 abstract 2
• 239000000178 monomer Substances 0.000 abstract 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 abstract 2
• RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 abstract 1
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
• NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 150000001875 compounds Chemical class 0.000 abstract 1
• 229910052736 halogen Inorganic materials 0.000 abstract 1
• 125000005843 halogen group Chemical group 0.000 abstract 1
• 150000002367 halogens Chemical class 0.000 abstract 1
• 150000002431 hydrogen Chemical class 0.000 abstract 1
• 239000000463 material Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 229960000907 methylthioninium chloride Drugs 0.000 abstract 1
• 125000000962 organic group Chemical group 0.000 abstract 1
• 230000003647 oxidation Effects 0.000 abstract 1
• 238000007254 oxidation reaction Methods 0.000 abstract 1
• 229910052760 oxygen Inorganic materials 0.000 abstract 1
• 239000001301 oxygen Substances 0.000 abstract 1
• 238000006116 polymerization reaction Methods 0.000 abstract 1
• 238000007342 radical addition reaction Methods 0.000 abstract 1
• 239000007870 radical polymerization initiator Substances 0.000 abstract 1
• 230000009257 reactivity Effects 0.000 abstract 1
• AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 abstract 1
• STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 abstract 1
• 230000001235 sensitizing effect Effects 0.000 abstract 1
• 239000000126 substance Substances 0.000 abstract 1
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
• 229920002554 vinyl polymer Polymers 0.000 abstract 1

Cited By (1)