Heteroatom-bridged heterofluorenes: a theoretical study on molecular structures and optoelectronic properties. Issue 6 (31st January 2020)
- Record Type:
- Journal Article
- Title:
- Heteroatom-bridged heterofluorenes: a theoretical study on molecular structures and optoelectronic properties. Issue 6 (31st January 2020)
- Main Title:
- Heteroatom-bridged heterofluorenes: a theoretical study on molecular structures and optoelectronic properties
- Authors:
- Qi, Yuanyuan
Chen, Cailin
Zheng, Chao
Tang, Yuting
Wan, Yifang
Jiang, He
Chen, Ting
Tao, Ye
Chen, Runfeng - Abstract:
- Abstract : A double heteroatom introduction strategy was proposed and theoretically investigated to construct highly rigid π-conjugated small molecules and polymers for optoelectronic applications. Abstract : Heteroatom incorporation is highly effective in tuning the molecular structures and optoelectronic properties of conjugated organic molecules. Here, we performed systematic theoretical studies on heteroatom-bridged heterofluorenes (BXF s) constructed by double heteroatom bridges of biphenyl to reveal the effects of heavily incorporated heteroatoms on molecular architecture and π-conjugation for different optoelectronic properties. Nine novel BXF s in three series were investigated and all of them exhibit promising potential optoelectronic properties owing to their highly fused molecular structure with heavy π-conjugation, although the introduction of different types and numbers of heteroatoms will lead to varied properties. Moreover, spiropolymers of BSiF and BGeF polymerized at the bridging position were also designed for the first time and found to have attractive optoelectronic properties of poly(BXF )s inherited from their monomers, demonstrating further the effectiveness of the bis-heteroatom introduction strategy in the construction of high-performance optoelectronic polymers. This heteroatom introduction strategy in constructing highly rigid π-conjugated materials could be applicable to other systems, representing a new concept advance to design novel conjugatedAbstract : A double heteroatom introduction strategy was proposed and theoretically investigated to construct highly rigid π-conjugated small molecules and polymers for optoelectronic applications. Abstract : Heteroatom incorporation is highly effective in tuning the molecular structures and optoelectronic properties of conjugated organic molecules. Here, we performed systematic theoretical studies on heteroatom-bridged heterofluorenes (BXF s) constructed by double heteroatom bridges of biphenyl to reveal the effects of heavily incorporated heteroatoms on molecular architecture and π-conjugation for different optoelectronic properties. Nine novel BXF s in three series were investigated and all of them exhibit promising potential optoelectronic properties owing to their highly fused molecular structure with heavy π-conjugation, although the introduction of different types and numbers of heteroatoms will lead to varied properties. Moreover, spiropolymers of BSiF and BGeF polymerized at the bridging position were also designed for the first time and found to have attractive optoelectronic properties of poly(BXF )s inherited from their monomers, demonstrating further the effectiveness of the bis-heteroatom introduction strategy in the construction of high-performance optoelectronic polymers. This heteroatom introduction strategy in constructing highly rigid π-conjugated materials could be applicable to other systems, representing a new concept advance to design novel conjugated small molecules and polymers for high-performance optoelectronic applications. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 22:Issue 6(2020)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 22:Issue 6(2020)
- Issue Display:
- Volume 22, Issue 6 (2020)
- Year:
- 2020
- Volume:
- 22
- Issue:
- 6
- Issue Sort Value:
- 2020-0022-0006-0000
- Page Start:
- 3675
- Page End:
- 3682
- Publication Date:
- 2020-01-31
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9cp06458c ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 12788.xml