Literature DB >> 11317287

New Concepts in Tetrathiafulvalene Chemistry.

José L. Segura1, Nazario Martín.   

Abstract

Tetrathiafulvalene (TTF) and its derivatives were originally prepared as strong electron-donor molecules for the development of electrically conducting materials. This Review emphasizes how TTF and its derivatives offer new and in some cases little-exploited possibilities at the molecular to the supramolecular levels, as well as in macromolecular aspects. TTF is a well-established molecule whose interest goes beyond the field of materials chemistry to be considered an important building block in supramolecular chemistry, crystal engineering, and in systems able to operate as machines. At the molecular level, TTF is a readily available molecule which displays a strong electron-donor ability. However, its use as a catalyst for radical-polar crossover reactions, thus mimicking samarium iodide chemistry, has only recently been addressed. Important goals have been achieved in the use of TTF at the macromolecular level where TTF-containing oligomers, polymers, and dendrimers have allowed the preparation of new materials that integrate the unique properties of TTF with the processability and stability that macromolecules display. The TTF molecule has also been successfully used in the construction of redox-active supramolecular systems. Thus, chemical sensors and redox-switchable ligands have been prepared from TTF while molecular shuttles and molecular switches have been prepared from TTF-containing rotaxanes and catenanes. A large synthetic effort has been devoted to the preparation of the so-called organic ferromagnets, many of which are derived from TTF. The main task in these systems is the introduction of ferromagnetic coupling between the conduction electrons and localized electrons. TTF has also played a prominent role in molecular electronics where TTF-containing D-sigma-A molecules have allowed the preparation of the first confirmed unimolecular rectifier. Recently, it has been confirmed that TTF can display efficient nonlinear optic (NLO) responses in the second and third harmonic generation as well as a good thermal stability. These findings can be combined with the redox ability of TTF as an external stimuli to provide a promising strategy for the molecular engineering of switchable NLO materials. Fullerenes endowed with TTF exhibit outstanding photophysical properties leading to charge-separated (CS) states that show remarkable lifetimes.

Entities:  

Year:  2001        PMID: 11317287     DOI: 10.1002/1521-3773(20010417)40:8<1372::aid-anie1372>3.0.co;2-i

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  28 in total

1.  Dipole Moment and Polarizability of Tunable Intramolecular Charge Transfer States in Heterocyclic π-Conjugated Molecular Dyads Determined by Computational and Stark Spectroscopic Study.

Authors:  Egmont J Rohwer; Maryam Akbarimoosavi; Steven E Meckel; Xunshan Liu; Yan Geng; Latévi Max Lawson Daku; Andreas Hauser; Andrea Cannizzo; Silvio Decurtins; Robert J Stanley; Shi-Xia Liu; Thomas Feurer
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2018-04-10       Impact factor: 4.126

2.  4-Bromo-5-[(2-bromo-ethyl)-sulfanyl]-1,3-dithiole-2-thione.

Authors:  Jing-Jing Ding; Yong-Hua Zhang; Bang-Tun Zhao; Gui-Rong Qu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-09-16

3.  3-(2-Thioxo-1,3-dithiol-4-ylsulfan-yl)-propane-nitrile.

Authors:  Bang-Tun Zhao; Jing-Jing Ding; Gui-Rong Qu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-10-04

4.  Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine.

Authors:  Jean Garnier; Alan R Kennedy; Leonard E A Berlouis; Andrew T Turner; John A Murphy
Journal:  Beilstein J Org Chem       Date:  2010-07-05       Impact factor: 2.883

5.  Dimethyl 2-(1-benzyl-2-oxoindolin-3-yl-idene)-1,3-dithiole-4,5-dicarboxyl-ate.

Authors:  Ayoob Bazgir
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-01-22

Review 6.  Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF.

Authors:  Erdal Ertas; İlknur Demirtas; Turan Ozturk
Journal:  Beilstein J Org Chem       Date:  2015-03-27       Impact factor: 2.883

7.  Tetrathiafulvalene-based azine ligands for anion and metal cation coordination.

Authors:  Awatef Ayadi; Aziz El Alamy; Olivier Alévêque; Magali Allain; Nabil Zouari; Mohammed Bouachrine; Abdelkrim El-Ghayoury
Journal:  Beilstein J Org Chem       Date:  2015-08-07       Impact factor: 2.883

8.  Copper ion salts of arylthiotetrathiafulvalenes: synthesis, structure diversity and magnetic properties.

Authors:  Longfei Ma; Jibin Sun; Xiaofeng Lu; Shangxi Zhang; Hui Qi; Lei Liu; Yongliang Shao; Xiangfeng Shao
Journal:  Beilstein J Org Chem       Date:  2015-05-20       Impact factor: 2.883

9.  Synthesis and redox behavior of new ferrocene-pi-extended-dithiafulvalenes: an approach for anticipated organic conductors.

Authors:  Abdelwareth A O Sarhan; Omar F Mohammed; Taeko Izumi
Journal:  Beilstein J Org Chem       Date:  2009-02-19       Impact factor: 2.883

10.  Synthesis and electrochemical proprieties of novel unsymmetrical bis-tetrathiafulvalenes and electrical conductivity of their charge transfer complexes with tetracyanoquinodimethane (TCNQ).

Authors:  Tahar Abbaz; Amel Bendjeddou; Abdelkrim Gouasmia; Zine Regainia; Didier Villemin
Journal:  Int J Mol Sci       Date:  2012-06-25       Impact factor: 6.208

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.