X-ray Diffraction, FT-IR, and 13C CP/MAS NMR Structural Studies of Solvated and Desolvated C-Methylcalix[4]resorcinarene-Reference-Cited by-同舟云学术

X-ray Diffraction, FT-IR, and 13C CP/MAS NMR Structural Studies of Solvated and Desolvated C-Methylcalix[4]resorcinarene

Published:2010-07-26 Issue:32 Volume:114 Page:10311-10320
ISSN:1520-6106
Container-title:The Journal of Physical Chemistry B
language:en
Short-container-title:J. Phys. Chem. B

Author:

Kuzmicz Rafal¹,Kowalska Violetta¹,Domagała Sławomir¹,Stachowicz Marcin¹,Woźniak Krzysztof¹,Kolodziejski Waclaw¹

Affiliation:

1. Department of Inorganic and Analytical Chemistry, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, Warszawa 02-097, Poland, and Department of Chemistry, University of Warsaw, Pasteura 1, Warszawa 02-093, Poland

Publisher

American Chemical Society (ACS)

Subject

Materials Chemistry,Surfaces, Coatings and Films,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jp1015565

Reference80 articles.

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4. Structurally new macrocycles from the resorcinol-aldehyde condensation. Configurational and conformational analyses by means of dynamic NMR, NOE, and T1 experiments

5. Molecular recognition. 5. Molecular recognition of sugars via hydrogen-bonding interaction with a synthetic polyhydroxy macrocycle

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