Unveiling the Nature of Chemical Bonds in Real Space-Reference-Cited by-同舟云学术

Unveiling the Nature of Chemical Bonds in Real Space

Published:2024-07-18 Issue:34 Volume:146 Page:23825-23830
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hara Takeshi¹^ORCID,Hasebe Masatoshi²,Tsuneda Takao³⁴^ORCID,Naito Toshio⁵,Nakamura Yuiga⁶^ORCID,Katayama Naoyuki¹^ORCID,Taketsugu Tetsuya³⁷,Sawa Hiroshi¹^ORCID

Affiliation:

1. Department of Applied Physics, Nagoya University, Nagoya 464-8603, Japan

2. Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo 060-8628, Japan

3. Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan

4. Graduate School of System Informatics, Kobe University, Kobe 657-0013, Japan

5. Graduate School of Science and Engineering, Ehime University, Matsuyama 790-8577, Japan

6. Japan Synchrotron Radiation Research Institute (JASRI), SPring-8, Hyogo 679-5198, Japan

7. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo 001-0021, Japan

Funder

Yamada Science Foundation

Nagoya University

Ministry of Education, Culture, Sports, Science and Technology

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c05673

Reference37 articles.

1. Effects of Spiroconjugation on the Calculated Singlet−Triplet Energy Gap in 2,2-Dialkoxycyclopentane-1,3-diyls and on the Experimental Electronic Absorption Spectra of Singlet 1,3-Diphenyl Derivatives. Assignment of the Lowest-Energy Electronic Transition of Singlet Cyclopentane-1,3-diyls

2. 1,2-Diazacyclopentane-3,5-diyl Diradicals: Electronic Structure and Reactivity

3. Dynamic solvent effects in radical–radical coupling reactions: an almost bottleable localised singlet diradical

4. Overlong CC Single Bonds

5. Long Carbon–Carbon Bonding beyond 2 Å in Tris(9-fluorenylidene)methane