A design concept of planar conjugated ladder oligomers of perylene bisimides and efficient synthetic strategy via regioselective photocyclization

Zhongyi Yuan; Yi Xiao; Xuhong Qian

doi:10.1039/b925605a

A design concept of planar conjugated ladder oligomers of perylene bisimides and efficient synthetic strategy via regioselective photocyclization

Zhongyi Yuan
, Yi Xiao^*
, Xuhong Qian

^*Corresponding author for this work

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

70 Scopus citations

Abstract

By photocyclization, benzene, thieno[3,2-b]thiophene, and fluorene units were embedded between the two perylene units. Symmetric oligomeric perylene bisimide 6 displays broad absorption and strong electron-accepting ability.

Original language	English
Pages (from-to)	2772-2774
Number of pages	3
Journal	Chemical Communications
Volume	46
Issue number	16
DOIs	https://doi.org/10.1039/b925605a
State	Published - 2010
Externally published	Yes

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@article{401e9a82a40541d882dc604eb5df6718,

title = "A design concept of planar conjugated ladder oligomers of perylene bisimides and efficient synthetic strategy via regioselective photocyclization",

abstract = "By photocyclization, benzene, thieno[3,2-b]thiophene, and fluorene units were embedded between the two perylene units. Symmetric oligomeric perylene bisimide 6 displays broad absorption and strong electron-accepting ability.",

author = "Zhongyi Yuan and Yi Xiao and Xuhong Qian",

year = "2010",

doi = "10.1039/b925605a",

language = "英语",

volume = "46",

pages = "2772--2774",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "16",

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T1 - A design concept of planar conjugated ladder oligomers of perylene bisimides and efficient synthetic strategy via regioselective photocyclization

AU - Yuan, Zhongyi

AU - Xiao, Yi

AU - Qian, Xuhong

PY - 2010

Y1 - 2010

N2 - By photocyclization, benzene, thieno[3,2-b]thiophene, and fluorene units were embedded between the two perylene units. Symmetric oligomeric perylene bisimide 6 displays broad absorption and strong electron-accepting ability.

AB - By photocyclization, benzene, thieno[3,2-b]thiophene, and fluorene units were embedded between the two perylene units. Symmetric oligomeric perylene bisimide 6 displays broad absorption and strong electron-accepting ability.

UR - https://www.scopus.com/pages/publications/77950476218

U2 - 10.1039/b925605a

DO - 10.1039/b925605a

M3 - 文章

C2 - 20369178

AN - SCOPUS:77950476218

SN - 1359-7345

VL - 46

SP - 2772

EP - 2774

JO - Chemical Communications

JF - Chemical Communications

IS - 16

ER -

A design concept of planar conjugated ladder oligomers of perylene bisimides and efficient synthetic strategy via regioselective photocyclization

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