Diastereoisomers of l-proline-linked trityl-nitroxide biradicals: synthesis and effect of chiral configurations on exchange interactions-Reference-Cited by-同舟云学术

Diastereoisomers of l-proline-linked trityl-nitroxide biradicals: synthesis and effect of chiral configurations on exchange interactions

Published:2018 Issue:19 Volume:9 Page:4381-4391
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Zhai Weixiang¹²³⁴⁵,Feng Yalan¹²³⁴⁵,Liu Huiqiang¹²³⁴⁵,Rockenbauer Antal⁶⁷⁸⁹¹⁰^ORCID,Mance Deni¹¹¹²¹³¹⁴¹⁵,Li Shaoyong¹²³⁴⁵,Song Yuguang¹²³⁴⁵,Baldus Marc¹¹¹²¹³¹⁴¹⁵^ORCID,Liu Yangping¹²³⁴⁵^ORCID

Affiliation:

1. Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics

2. School of Pharmacy

3. Tianjin Medical University

4. Tianjin 300070

5. P. R. China

6. Institute of Materials and Environmental Chemistry

7. Hungarian Academy of Sciences

8. Department of Physics

9. Budapest University of Technology and Economics

10. 1111 Budapest

11. NMR Spectroscopy

12. Bijvoet Center for Biomolecular Research

13. Utrecht University

14. 3584 CH Utrecht

15. The Netherlands

Abstract

The chiral configuration of the two radical parts is a crucial factor controlling the exchange interactions and DNP properties of trityl-nitroxide biradicals.

Funder

National Natural Science Foundation of China

Nederlandse Organisatie voor Wetenschappelijk Onderzoek

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/SC/C8SC00969D

Reference53 articles.

1. High Frequency Dynamic Nuclear Polarization

2. Dynamic Nuclear Polarization Surface Enhanced NMR Spectroscopy