Novel enantiopure bis(pyrrolo)tetrathiafulvalene donors exhibiting chiral crystal packing arrangements-Reference-Cited by-同舟云学术

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Novel enantiopure bis(pyrrolo)tetrathiafulvalene donors exhibiting chiral crystal packing arrangements

Published:2009 Issue:6 Volume:11 Page:993
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Yang Songjie,Brooks Andrew C.,Martin Lee,Day Peter,Li Hongchao,Horton Peter,Male Louise,Wallis John D.

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2009/CE/B822009N

Reference20 articles.

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

2. Electrical Magnetochiral Anisotropy

3. Magneto-chiral anisotropy in charge transport through single-walled carbon nanotubes

4. Synthetic strategies to chiral organosulfur donors related to bis(ethylenedithio)tetrathiafulvalene

5. Synthesis of bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) derivatives functionalised with two, four or eight hydroxyl groups

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1. Non-Symmetric Bispyrrolotetrathiafulvalene Building Blocks;Synthesis;2023-01-26

2. Enantiopure and racemic radical-cation salts of B(mandelate)₂⁻ and B(2-chloromandelate)₂⁻ anions with BEDT-TTF;Dalton Transactions;2022

3. Donor-Type Nickel–Dithiolene Complexes Fused with Bulky Cycloalkane Substituents and Their Application in Molecular Conductors;Crystals;2021-09-23

4. Modern History of Organic Conductors: An Overview;Crystals;2021-07-20

5. Main-Group-Based Electro- and Photoactive Chiral Materials;Chemical Reviews;2019-04-03

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