Long Carbon–Carbon Bonding beyond 2 Å in Tris(9-fluorenylidene)methane-Reference-Cited by-同舟云学术

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

Published:2021-08-30 Issue:35 Volume:143 Page:14360-14366
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Kubo Takashi¹²^ORCID,Suga Yuki¹,Hashizume Daisuke³^ORCID,Suzuki Hiroki⁴,Miyamoto Tatsuya⁴⁵,Okamoto Hiroshi⁴⁵^ORCID,Kishi Ryohei⁶⁷⁸^ORCID,Nakano Masayoshi⁶²⁹⁷⁸^ORCID

Affiliation:

1. Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan

2. Innovative Catalysis Science Division (ICS), Institute for Open and Transdisciplinary Research Initiatives (OTRI), Osaka University, Suita, Osaka 565-0871, Japan

3. RIKEN Center for Emergent Matter Science (CEMS), Wako, Saitama 351-0198, Japan

4. Department of Advanced Materials Science, University of Tokyo, Kashiwa, Chiba 277-8561, Japan

5. National Institute of Advanced Industrial Science and Technology (AIST)-University of Tokyo Advanced Operando-Measurement Technology Open Innovation Laboratory (OPERANDO-OIL), AIST, Kashiwa, Chiba 277-8561, Japan

6. Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan

7. Center for Quantum Information and Quantum Biology (QIQB), Osaka University, Toyonaka, Osaka 560-8531 Japan

8. Research Center for Solar Energy Chemistry (RCSEC), Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan

9. Center for Spintronics Research Network (CSRN), Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan

Funder

Core Research for Evolutional Science and Technology

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c07431

Reference37 articles.

1. Strikingly Long C···C Distances in 1,2-Disubstituted ortho-Carboranes and Their Dianions

2. Preparation and structural study of naphtho- and anthrocyclobutene derivatives which have extremely long C–C bonds

3. The Nature of the Long Bond in 3,8-Dichloro-1,1,2,2-tetraphenylcyclobuta[b]naphthene

4. [2+2] Cycloaddition Products of Tetradehydrodianthracene: Experimental and Theoretical Proof of Extraordinary Long CC Single Bonds

5. Determination of the central bond length in hexaarylethanes by nutation NMR spectroscopy

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Theoretical Study of an Authentic Hydrocarbon Ion Pair;ACS Omega;2024-08-02

2. Experimental molecular structures in the gas phase at the upper size limit: The case of Si6Tip6;The Journal of Chemical Physics;2024-08-02

3. Catalytic chemical recycling and upcycling of polyolefin plastics;Giant;2024-08

4. Unveiling the Nature of Chemical Bonds in Real Space;Journal of the American Chemical Society;2024-07-18

5. Designing Principles for Ultrashort H⋯H Nonbonded Contacts and Ultralong CC Bonds;Electron Density;2024-07-05