Contrasting crystal packing arrangements in triiodide salts of radical cations of chiral bis(pyrrolo[3,4-d])tetrathiafulvalenes-Reference-Cited by-同舟云学术

Contrasting crystal packing arrangements in triiodide salts of radical cations of chiral bis(pyrrolo[3,4-d])tetrathiafulvalenes

Published:2015 Issue:38 Volume:17 Page:7354-7362
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Martin Lee¹²³,Yang Songjie¹²³,Brooks Andrew C.¹²³⁴⁵,Horton Peter N.⁵⁶⁷,Male Louise⁵⁶⁷,Moulfi Ourida¹²³,Harmand Lydie¹²³,Day Peter⁴⁵⁸,Clegg William⁹¹⁰¹¹,Harrington Ross W.⁹¹⁰¹¹,Wallis John D.¹²³

Affiliation:

1. School of Science and Technology

2. Nottingham Trent University

3. Nottingham NG11 8NS, UK

4. University College London

5. Department of Chemistry

6. University of Southampton

7. Southampton, UK

8. London WC1H 0AJ, UK

9. School of Chemistry

10. Newcastle University

11. Newcastle upon Tyne, UK

Abstract

Triiodides are arranged in head to tail pairs, infinite lines or a castellated arrangement in the radical cation salts of chiral bis(N(1-arylethyl))pyrrolo-tetrathiafulvalene salts.

Funder

Engineering and Physical Sciences Research Council

Royal Society

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CE/C5CE01430A

Reference51 articles.

1. Chiral metals? A chiral substrate for organic conductors and superconductors

2. Structures and Electrical Properties of Some New Organic Conductors Derived from the Donor Molecule TMET (S,S,S,S,-Bis(dimethylethylenedithio) tetrathiafulvalene)