A novel diacid chloride, 2-（4-chlorocarboxyphenyl）-4-[3,5-dimethyl-4-（4-chlorocarbo-xylphenoxy）phenyl]-2,3-phthalazin-l-one 2, was synthesized and used for the preparation of polyarylates with inherent viscosities...A novel diacid chloride, 2-（4-chlorocarboxyphenyl）-4-[3,5-dimethyl-4-（4-chlorocarbo-xylphenoxy）phenyl]-2,3-phthalazin-l-one 2, was synthesized and used for the preparation of polyarylates with inherent viscosities of 0.25-0.37 dL·g^-1. The glass transition temperatures of polyarylates were in the range of 217-272℃. The temperatures at 10% weight loss of polyarylates were found to be in the range of 434-464℃ in nitrogen atmosphere and their structure was confirmed by FTIR and IH NMR. The amorphous polyarylates exhibited excellent solubility in a variety of solvents such as NMP, DMAc, DMF and chloroform.展开更多
In the case of Pd(PPh3)4 as catalyst and toluene as reaction solvent, the desired biaryls and polyaryls were synthesized in excellent yield and on a large scale.
Substituted polyaryls were synthesized successfully via sterically hindered double Suzuki cross-couplings of arylboronic acids with aryl dibromides in the presence of Pd（PPh3）4 and KOtBu within a very short time. ？...Substituted polyaryls were synthesized successfully via sterically hindered double Suzuki cross-couplings of arylboronic acids with aryl dibromides in the presence of Pd（PPh3）4 and KOtBu within a very short time. ？2009 Guo Hua Gao. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
文摘A novel diacid chloride, 2-（4-chlorocarboxyphenyl）-4-[3,5-dimethyl-4-（4-chlorocarbo-xylphenoxy）phenyl]-2,3-phthalazin-l-one 2, was synthesized and used for the preparation of polyarylates with inherent viscosities of 0.25-0.37 dL·g^-1. The glass transition temperatures of polyarylates were in the range of 217-272℃. The temperatures at 10% weight loss of polyarylates were found to be in the range of 434-464℃ in nitrogen atmosphere and their structure was confirmed by FTIR and IH NMR. The amorphous polyarylates exhibited excellent solubility in a variety of solvents such as NMP, DMAc, DMF and chloroform.
基金Support from the University of Science and Technology of China the National Natural Science Foundation of China are gratefully acknowledged (NO. 50073021).
文摘In the case of Pd(PPh3)4 as catalyst and toluene as reaction solvent, the desired biaryls and polyaryls were synthesized in excellent yield and on a large scale.
基金supported by National Natural Science Foundation of China(No.20873041)Shanghai Leading Academic Discipline Project(No.B409).
文摘Substituted polyaryls were synthesized successfully via sterically hindered double Suzuki cross-couplings of arylboronic acids with aryl dibromides in the presence of Pd（PPh3）4 and KOtBu within a very short time. ？2009 Guo Hua Gao. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
