Hindered Rotation in Diphenylmethane Derivatives. Electrostatic vs Charge-Transfer and Homoconjugative Aryl−Aryl Interactions-Reference-Cited by-同舟云学术

Hindered Rotation in Diphenylmethane Derivatives. Electrostatic vs Charge-Transfer and Homoconjugative Aryl−Aryl Interactions

Published:1998-02-01 Issue:4 Volume:120 Page:673-679
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Martínez A. García¹,Barcina J. Osío¹,Cerezo A. de Fresno¹,Rivas R. Gutiérrez¹

Affiliation:

1. Contribution from the Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense, Ciudad Universitaria, 28040 Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja971388%2B

Reference48 articles.

1. Arene—Arene Interactions: Electrostatic or Charge Transfer?

2. Polar Interactions between Stackedπ Systems in Fluorinated 1,8-Diarylnaphthalenes: Importance of Quadrupole Moments in Molecular Recognition

3. 7,7-Diphenylnorbornane: The first cofacial diphenylmethane derivative

4. Conformational properties of some o-substituted 1,1-diphenylethanes

5. The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroids

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