Sulfamoyl nitrenes: singlet or triplet ground state?-Reference-Cited by-同舟云学术

Sulfamoyl nitrenes: singlet or triplet ground state?

Published:2018 Issue:48 Volume:54 Page:6136-6139
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Lu Yan¹²³⁴⁵,Li Hongmin¹²³⁴⁵,Abe Manabu⁶⁷⁸⁹¹⁰,Bégué Didier¹¹¹²¹³¹⁴^ORCID,Wan Huabin¹²³⁴⁵,Deng Guohai¹²³⁴⁵,Xu Jian¹²³⁴⁵,Liu Kun¹¹⁵¹⁶⁵,Zeng Xiaoqing¹²³⁴⁵^ORCID

Affiliation:

1. College of Chemistry

2. Chemical Engineering and Materials Science

3. Soochow University

4. Suzhou 215123

5. China

6. Department of Chemistry

7. Graduate School of Science

8. Hiroshima University

9. Higashi-Hiroshima Hiroshima 739-8526

10. Japan

11. Institut Pluridisciplinaire de Recherche sur l’Environnement et les Matériaux

12. Universitéde Pau et des Pays de l’Adour

13. Pau 64000

14. France

15. Tianjin Normal University

16. Tianjin

Abstract

Two prototypical sulfamoyl nitrenes R₂NS(O)₂–N (R = H and Me) in the triplet state were generated via the closed-shell singlet state by passing a low-energy minimum energy crossing point (MECP).

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC03278E

Reference48 articles.

1. Inverting Steric Effects: Using “Attractive” Noncovalent Interactions To Direct Silver-Catalyzed Nitrene Transfer

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3. Trifluoromethanesulfonamides and Related Compounds

4. Sulfamic Acid and Its N- and O-Substituted Derivatives

5. Mapping the lipid-exposed regions in the Torpedo californica nicotinic acetylcholine receptor

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