Multistep Electron Transfer Systems Containing [2.2]- or [3.3]Paracyclophane
Author:
Affiliation:
1. The Institute of Scientific and Industrial Research (SANKEN), Osaka University, Mihogaoka 8-1, Ibaraki, Osaka 567-0047, Japan
2. Institute for Materials Chemistry and Engineering (IMCE), Kyushu University, Hakozaki 6-10-1, Fukuoka 812-8581, Japan
Funder
Ministry of Education, Culture, Sports, Science, and Technology
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.5b11766
Reference34 articles.
1. Cyclophane chemistry: bent and battered benzene rings
2. Cyclophanes containing large polycyclic aromatic hydrocarbons
3. Synthesis, Structure, and Transannular π−π Interaction of Three- and Four-Layered [3.3]Paracyclophanes
4. Synthesis of a“Molecular Pinwheel”:[3.3.3.3.3.3](1,2,3,4,5,6)Cyclophane
5. The radical ions of 4,5,7,8-tetramethyl[2.2]paracyclophane
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2. [2.2]‐ and [3.3]Paracyclophane as Bridging Units in Organic Dyads for Visible‐Light‐Driven Dye‐Sensitized Hydrogen Production;Chemistry – A European Journal;2022-06-17
3. Self-Assembling [n.n]Paracyclophanes: A Structure–Property Relationship Study;The Journal of Organic Chemistry;2019-12-11
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5. Donor-Donor′-Acceptor Triads Based on [3.3]Paracyclophane with a 1,4-Dithiafulvene Donor and a Cyanomethylene Acceptor: Synthesis, Structure, and Electrochemical and Photophysical Properties;Chemistry - A European Journal;2018-07-06
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