The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility

J. E. Anthony; M. M. Payne; C. A. Landis; J. E. Bullock

doi:10.1109/DRC.2004.1367875

The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility

J. E. Anthony, M. M. Payne, C. A. Landis, J. E. Bullock

Chemistry

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

Abstract

The technique to improve the performance of acenes was investigated using molecular engineering methods. The stability and basic electronic properties of acenes were also discussed. The charge-carrier mobility in acenes was improved by decreasing intermolecular spacing between π-faces in the solid state. It was found that the dioxolane-substituted pentacene exhibits both a blue-shift in absorption and emission along with an increase in fluorescence quantum yield.

Original language	English
Title of host publication	Device Research Conference - Conference Digest, 62nd DRC
Pages	221-222
Number of pages	2
DOIs	https://doi.org/10.1109/DRC.2004.1367875
State	Published - 2004
Event	Device Research Conference - Conference Digest, 62nd DRC - Notre Dame, IN, United States Duration: Jun 21 2004 → Jun 23 2004

Publication series

Name	Device Research Conference - Conference Digest, DRC
ISSN (Print)	1548-3770

Conference

Conference	Device Research Conference - Conference Digest, 62nd DRC
Country/Territory	United States
City	Notre Dame, IN
Period	6/21/04 → 6/23/04

ASJC Scopus subject areas

General Engineering

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10.1109/DRC.2004.1367875

Cite this

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title = "The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility",

abstract = "The technique to improve the performance of acenes was investigated using molecular engineering methods. The stability and basic electronic properties of acenes were also discussed. The charge-carrier mobility in acenes was improved by decreasing intermolecular spacing between π-faces in the solid state. It was found that the dioxolane-substituted pentacene exhibits both a blue-shift in absorption and emission along with an increase in fluorescence quantum yield.",

author = "Anthony, \{J. E.\} and Payne, \{M. M.\} and Landis, \{C. A.\} and Bullock, \{J. E.\}",

year = "2004",

doi = "10.1109/DRC.2004.1367875",

language = "English",

isbn = "0780382846",

series = "Device Research Conference - Conference Digest, DRC",

pages = "221--222",

booktitle = "Device Research Conference - Conference Digest, 62nd DRC",

note = "Device Research Conference - Conference Digest, 62nd DRC ; Conference date: 21-06-2004 Through 23-06-2004",

}

Anthony, JE, Payne, MM, Landis, CA & Bullock, JE 2004, The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility. in Device Research Conference - Conference Digest, 62nd DRC., VII.A.-1, Device Research Conference - Conference Digest, DRC, pp. 221-222, Device Research Conference - Conference Digest, 62nd DRC, Notre Dame, IN, United States, 6/21/04. https://doi.org/10.1109/DRC.2004.1367875

The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility. / Anthony, J. E.; Payne, M. M.; Landis, C. A. et al.
Device Research Conference - Conference Digest, 62nd DRC. 2004. p. 221-222 VII.A.-1 (Device Research Conference - Conference Digest, DRC).

Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

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PY - 2004

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N2 - The technique to improve the performance of acenes was investigated using molecular engineering methods. The stability and basic electronic properties of acenes were also discussed. The charge-carrier mobility in acenes was improved by decreasing intermolecular spacing between π-faces in the solid state. It was found that the dioxolane-substituted pentacene exhibits both a blue-shift in absorption and emission along with an increase in fluorescence quantum yield.

AB - The technique to improve the performance of acenes was investigated using molecular engineering methods. The stability and basic electronic properties of acenes were also discussed. The charge-carrier mobility in acenes was improved by decreasing intermolecular spacing between π-faces in the solid state. It was found that the dioxolane-substituted pentacene exhibits both a blue-shift in absorption and emission along with an increase in fluorescence quantum yield.

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The molecular engineering of acenes: Avoidnig the drawbacks of improved solubility

Abstract

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