Toroidal Interaction and Propeller Chirality of Hexaarylbenzenes. Dynamic Domino Inversion Revealed by Combined Experimental and Theoretical Circular Dichroism Studies-Reference-Cited by-同舟云学术

Toroidal Interaction and Propeller Chirality of Hexaarylbenzenes. Dynamic Domino Inversion Revealed by Combined Experimental and Theoretical Circular Dichroism Studies

Published:2016-02-17 Issue:5 Volume:7 Page:783-788
ISSN:1948-7185
Container-title:The Journal of Physical Chemistry Letters
language:en
Short-container-title:J. Phys. Chem. Lett.

Author:

Kosaka Tomoyo¹,Inoue Yoshihisa¹,Mori Tadashi¹

Affiliation:

1. Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamada-oka, Suita 565-0871, Japan

Funder

Iketani Science and Technology Foundation

Matching Planner Program (JST)

Shorai Foundation for Science and Technology

Kurata Memorial Hitachi Science and Technology Foundation

Tokuyama Science Foundation

Toyota Physical and Chemical Research Institute

Izumi Science and Technology Foundation

Grant-in-Aids for Scientific Research, Challenging Exploratory Research, and on Innovative Areas "Photosynergetics" (MEXT/JSPS)

Publisher

American Chemical Society (ACS)

Subject

General Materials Science,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jpclett.6b00179

Reference26 articles.

1. Hexaarylbenzenes—Prospects for Toroidal Delocalization of Charge and Energy

2. Through-Space (Cofacial) π-Delocalization among Multiple Aromatic Centers: Toroidal Conjugation in Hexaphenylbenzene-like Radical Cations

3. Very Fast Electron Migrations within p-Doped Aromatic Cofacial Arrays Leading to Three-Dimensional (Toroidal) π-Delocalization

4. Computational Study of Electron Delocalization in Hexaarylbenzenes

5. Synthesis, Structure, and Evaluation of the Effect of Multiple Stacking on the Electron-Donor Properties of π-Stacked Polyfluorenes

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