Molecular tetrominoes: selective masking of the donor π-face to control the configuration of donor-acceptor complexes.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
05 01 2022
Historique:
pubmed: 15 12 2021
medline: 15 12 2021
entrez: 14 12 2021
Statut: epublish

Résumé

Understanding the doping mechanism in organic semiconductors and generating molecular design rules to control the doping process are crucial for improving the performance of organic electronics. Even though controlling the location and orientation of the dopant along the semiconductor backbone is an important step in the doping mechanism, studies in this direction are scarce as it is a challenging task. To address this, herein, we incorporated π-face masked (strapped) units in 1,4-bis(phenylethynylene)benzene (donor) to control the acceptor (dopant) location along the trimer, donor-acceptor binding strength, and acceptor ionization. Two strapped trimers, PCP and CPC, are synthesized with control over the location of the strapped repeat unit in the trimer. The trimers are complexed with the 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) acceptor in solution. DFT calculations show that DDQ residing on the non-strapped repeat unit (the percentage of this configuration is at least

Identifiants

pubmed: 34904145
doi: 10.1039/d1ob02293h
doi:

Types de publication

Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-386

Auteurs

Jenna L Sartucci (JL)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.
Institute for Soft Matter Synthesis and Metrology, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA.

Arindam Maity (A)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.
Institute for Soft Matter Synthesis and Metrology, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA.

Manikandan Mohanan (M)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.
Institute for Soft Matter Synthesis and Metrology, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA.

Jeffery Bertke (J)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.

Miklos Kertesz (M)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.
Institute for Soft Matter Synthesis and Metrology, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA.

Nagarjuna Gavvalapalli (N)

Department of Chemistry, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA. ng554@georgetown.edu.
Institute for Soft Matter Synthesis and Metrology, Georgetown University, 3700 O St NW, Washington, D.C., 20057, USA.

Classifications MeSH