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Synthesis of Network Polymers Containing Triazine <i>via</i> Direct Arylation of Fluoroarenes and Their Properties
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- HAYASHI Shotaro
- Department of Applied Chemistry, National Defense Academy
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- TOGAWA Yuki
- Department of Applied Chemistry, National Defense Academy
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- ASANO Atsushi
- Department of Applied Chemistry, National Defense Academy
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- NISHI Koji
- Department of Applied Chemistry, National Defense Academy
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- YAMAMOTO Shin-ichi
- Department of Applied Chemistry, National Defense Academy
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- KOIZUMI Toshio
- Department of Applied Chemistry, National Defense Academy
Bibliographic Information
- Other Title
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- フルオロアレーンの直接的アリール化による含トリアジンネットワークポリマーの合成とその特性
- フルオロアレーン ノ チョクセツテキ アリールカ ニ ヨル ガン トリアジンネットワークポリマー ノ ゴウセイ ト ソノ トクセイ
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Description
The direct arylation synthesis of π-conjugated network polymers (conjugated microporous polymers: CMP) containing fluoroarene and triazine moieties was successfully achieved. The direct arylation of 1,2,4,5-tetrafluorobenzene or 1,3,5-trifluorobenzene with a tribromoarene having a triazine core under two reaction conditions (Conditions a: in DMAc, Conditions b: in toluene) gave four types of CMPs (CMP1a, CMP1b, CMP2a and CMP2b). Brunauer-Emmett-Teller (BET) surface area of CMP2a and CMP2b was higher than that of CMP1a and CMP1b because of a higher number of branches. The solvents used for the direct arylation polycondensation thus strongly affected the structure of the resulting CMPs.
Journal
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- KOBUNSHI RONBUNSHU
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KOBUNSHI RONBUNSHU 74 (6), 453-459, 2017
The Society of Polymer Science, Japan
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Details 詳細情報について
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- CRID
- 1390282681502097152
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- NII Article ID
- 130006218863
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- NII Book ID
- AN00085011
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- ISSN
- 18815685
- 03862186
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- NDL BIB ID
- 028674160
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- Text Lang
- ja
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- Article Type
- journal article
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- Data Source
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- JaLC
- NDL Search
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed