Hydrogen versus tetrel bonds in complexes of 3-oxetanone with water and formaldehyde-Reference-Cited by-同舟云学术

Hydrogen versus tetrel bonds in complexes of 3-oxetanone with water and formaldehyde

Published:2021 Issue:12 Volume:23 Page:7295-7301
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Chen Junhua¹²³⁴⁵,Wang Hao¹²³⁴⁵,Kisiel Zbigniew⁶⁷⁸⁹¹⁰^ORCID,Gou Qian¹²³⁴⁵^ORCID,Caminati Walther¹¹¹²¹³¹⁴¹⁵^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Chongqing University

3. No. 55 Daxuecheng South Rd

4. Shapingba

5. China

6. Institute of Physics

7. Polish Academy of Sciences

8. Al. Lotników 32/46

9. Warszawa 02-668

10. Poland

11. Dipartimento di Chimica “G. Ciamician”

12. Università di Bologna

13. Via Selmi 2

14. Bologna I-40126

15. Italy

Abstract

The ability and preference of 3-oxetanone to form hydrogen or tetrel bonds have been investigated in its complexes with water and formaldehyde by using Fourier transform microwave spectroscopy complemented with quantum chemical calculations.

Funder

Natural Science Foundation of Chongqing

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

China Sponsorship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CP/D1CP00239B

Reference59 articles.

1. Oxetanes as Versatile Elements in Drug Discovery and Synthesis

2. Reactions of Oxetan-3-tert-butylsulfinimine for the Preparation of Substituted 3-Aminooxetanes

3. Passerini reactions for the efficient synthesis of 3,3-disubstituted oxetanes

4. Ring Expansion of 3-Oxetanone-Derived Spirocycles: Facile Synthesis of Saturated Nitrogen Heterocycles

5. Oxetanes: Recent Advances in Synthesis, Reactivity, and Medicinal Chemistry

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