SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS
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SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS
Vol. 14, Issue 3, Pages: 248-254(1996)
Affiliations:
1. Institute of Chemistry
2. Academia Sinica
3. Beijing 100080
Author bio:
Funds:
DOI:
CLC:TQ317
Published:20 September 1996
Accepted:
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[1]孙学慧,杨玉昆.SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS[J].Chinese Journal of Polymer Science,1996,{4}(03):248-254.
SUN Xuehui, YANG Yukun. SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS[J]. 1996, 14(3): 248-254.
[1]孙学慧,杨玉昆.SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS[J].Chinese Journal of Polymer Science,1996,{4}(03):248-254.DOI:
SUN Xuehui, YANG Yukun. SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS[J]. 1996, 14(3): 248-254.DOI:
SYNTHESIS AND PHOTOCHROMISM OF ACRYLIC ESTER COPOLYMERS BEARING PENDANT VIOLOGEN GROUPS
A series of acrylic ester copolymers with viologen group as pendant were synthesizedthrough the reaction of MMA-EBA (Ethenyl bromoacetate) copolymer with 4-(4’-pyridyl)-N-alkyl (or arylalkyl) pyridiniums. These viologen copolymers can exchange their anionwith NH
4
PF
6
in methanol to improve their solubility in organic solvents such as DMFand acetone. Compared with the corresponding low molecular viologens
these viologencopolymers have relatively lower color development rate under UV light and fade fasterin air due to less affinity to photo-reductant and deficiency of association between theircation radicals. Their photofatigue resistant ability is also slightly better than that of lowmolecular vinlogens.
Abstract
A series of acrylic ester copolymers with viologen group as pendant were synthesizedthrough the reaction of MMA-EBA (Ethenyl bromoacetate) copolymer with 4-(4’-pyridyl)-N-alkyl (or arylalkyl) pyridiniums. These viologen copolymers can exchange their anionwith NH
4
PF
6
in methanol to improve their solubility in organic solvents such as DMFand acetone. Compared with the corresponding low molecular viologens
these viologencopolymers have relatively lower color development rate under UV light and fade fasterin air due to less affinity to photo-reductant and deficiency of association between theircation radicals. Their photofatigue resistant ability is also slightly better than that of lowmolecular vinlogens.
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