Relative Position and Relative Rotation in Supramolecular Systems through the Analysis of the Principal Axes of Inertia: Ferrocene/Cucurbit[7]uril and Ferrocenyl Azide/β-Cyclodextrin Case Studies-Reference-Cited by-同舟云学术

Relative Position and Relative Rotation in Supramolecular Systems through the Analysis of the Principal Axes of Inertia: Ferrocene/Cucurbit[7]uril and Ferrocenyl Azide/β-Cyclodextrin Case Studies

Published:2020-03-06 Issue:10 Volume:5 Page:5013-5025
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Anconi Cleber P. A.¹^ORCID

Affiliation:

1. Laboratório de Quı́mica Fundamental (LQF), Departamento de Quı́mica, Universidade Federal de Lavras, 37200-900 Lavras, MG, Brazil

Funder

Funda??o de Amparo ? Pesquisa do Estado de Minas Gerais

Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b03914

Reference60 articles.

1. Complexation of Ferrocene Derivatives by the Cucurbit[7]uril Host: A Comparative Study of the Cucurbituril and Cyclodextrin Host Families

2. Cucurbituril Homologues and Derivatives: New Opportunities in Supramolecular Chemistry

3. Electronic Structure, Molecular Electrostatic Potential, and NMR Chemical Shifts in Cucurbit[n]urils (n = 5−8), Ferrocene, and Their Complexes

4. Density-functional exchange-energy approximation with correct asymptotic behavior

5. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

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