Highly fluorinated benzobisbenzothiophenes

Yongfeng Wang; Sean R. Parkin; Johannes Gierschner; Mark D. Watson

doi:10.1021/ol8003468

Highly fluorinated benzobisbenzothiophenes

Yongfeng Wang
, Sean R. Parkin
, Johannes Gierschner
, Mark D. Watson

Chemistry

Research output: Contribution to journal › Article › peer-review

137 Scopus citations

Abstract

(Figure Presented) Expedient, facile syntheses of highly fluorinated benzobisbenzothiophenes (BBBT) are reported. Defined peripheral arrangements of sulfur and fluorine atoms lead to extensive crystalline networks of edge-to-edge S-F close contacts. The effects of various substitution patterns on self-assembly and electronic properties are described.

Original language	English
Pages (from-to)	3307-3310
Number of pages	4
Journal	Organic Letters
Volume	10
Issue number	15
DOIs	https://doi.org/10.1021/ol8003468
State	Published - 2008

ASJC Scopus subject areas

Biochemistry
Physical and Theoretical Chemistry
Organic Chemistry

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10.1021/ol8003468

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@article{e526b11b5aaf4f9eb4f8a632ca7228bf,

title = "Highly fluorinated benzobisbenzothiophenes",

abstract = "(Figure Presented) Expedient, facile syntheses of highly fluorinated benzobisbenzothiophenes (BBBT) are reported. Defined peripheral arrangements of sulfur and fluorine atoms lead to extensive crystalline networks of edge-to-edge S-F close contacts. The effects of various substitution patterns on self-assembly and electronic properties are described.",

author = "Yongfeng Wang and Parkin, \{Sean R.\} and Johannes Gierschner and Watson, \{Mark D.\}",

year = "2008",

doi = "10.1021/ol8003468",

language = "English",

volume = "10",

pages = "3307--3310",

number = "15",

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TY - JOUR

T1 - Highly fluorinated benzobisbenzothiophenes

AU - Wang, Yongfeng

AU - Parkin, Sean R.

AU - Gierschner, Johannes

AU - Watson, Mark D.

PY - 2008

Y1 - 2008

N2 - (Figure Presented) Expedient, facile syntheses of highly fluorinated benzobisbenzothiophenes (BBBT) are reported. Defined peripheral arrangements of sulfur and fluorine atoms lead to extensive crystalline networks of edge-to-edge S-F close contacts. The effects of various substitution patterns on self-assembly and electronic properties are described.

AB - (Figure Presented) Expedient, facile syntheses of highly fluorinated benzobisbenzothiophenes (BBBT) are reported. Defined peripheral arrangements of sulfur and fluorine atoms lead to extensive crystalline networks of edge-to-edge S-F close contacts. The effects of various substitution patterns on self-assembly and electronic properties are described.

UR - https://www.scopus.com/pages/publications/57349092565

UR - https://www.scopus.com/pages/publications/57349092565#tab=citedBy

U2 - 10.1021/ol8003468

DO - 10.1021/ol8003468

M3 - Article

C2 - 18610977

AN - SCOPUS:57349092565

SN - 1523-7060

VL - 10

SP - 3307

EP - 3310

JO - Organic Letters

JF - Organic Letters

IS - 15

ER -

Highly fluorinated benzobisbenzothiophenes

Abstract

ASJC Scopus subject areas

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