Hydrogen bonding and dominant conformations of hydrated sugar analogue complexes using tetrahydrofurfuryl alcohol as the model sugar molecule-Reference-Cited by-同舟云学术

Hydrogen bonding and dominant conformations of hydrated sugar analogue complexes using tetrahydrofurfuryl alcohol as the model sugar molecule

Published:2018 Issue:10 Volume:20 Page:7351-7360
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Jin Shan¹²³⁴⁵,Hu Yongjun¹²³⁴⁵^ORCID,Wang Pengchao¹²³⁴⁵,Zhan Huaqi¹²³⁴⁵,Lu Qiao¹²³⁴⁵,Liu Fuyi⁶⁷⁸⁵,Sheng Liusi⁶⁷⁸⁵

Affiliation:

1. MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science

2. College of Biophotonics

3. South China Normal University

4. Guangzhou 510631

5. P. R. China

6. National Synchrotron Radiation Laboratory

7. University of Science and Technology of China

8. Hefei

Abstract

Water molecules, which serve as both hydrogen bond donors and acceptors, have been found to influence the conformational landscape of gas-phase phenyl-β-d-glucopyranoside.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CP/C7CP07935D

Reference81 articles.

1. L. Stryer , Biochemistry , W.H. Freeman and Company , New York , 4th edn, 1995

2. Sugars in the gas phase: the spectroscopy and structure of jet-cooled phenyl β-D-glucopyranoside

3. Hydrated Sugars in the Gas Phase: Spectroscopy and Conformation of Singly Hydrated Phenyl β-d-Glucopyranoside

4. Hydrogen Bonding and Cooperativity in Isolated and Hydrated Sugars: Mannose, Galactose, Glucose, and Lactose

5. Adding water to sugar: A spectroscopic and computational study of α- and β-phenylxyloside in the gas phase

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