том 69 издание 13 страницы 4492-4499

Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers

Тип публикацииJournal Article
Дата публикации2004-06-01
scimago Q2
wos Q1
БС1
SJR0.737
CiteScore6.1
Impact factor3.6
ISSN00223263, 15206904
Organic Chemistry
Краткое описание
A series of novel conjugated homo (16a,b) and heterodimers (20) of pi-extended tetrathiafulvalenes with p-quinodimethane structures (exTTFs) linked by a conjugative vinyl spacer have been prepared by olefination Wittig-Horner reaction from the corresponding quinones (14, 19) and phosphonates (15a,b). The redox properties, determined by cyclic voltammetry, reveal a strong donor character and the presence of only one four-electron oxidation wave to form the tetracation species at oxidation potential values quite similar to those found for the related monomers. Theoretical calculations (PM3) show a planar central stilbene moiety and highly distorted exTTF units. The electronic spectra support as well as the electrochemical data and theoretical calculation the lack of significant communication between the exTTF units.
Найдено 
Найдено 

Топ-30

Журналы

1
2
3
Chemistry - A European Journal
3 публикации, 13.04%
Chemical Communications
3 публикации, 13.04%
Tetrahedron Letters
2 публикации, 8.7%
Journal of Materials Chemistry A
2 публикации, 8.7%
Computational and Theoretical Chemistry
1 публикация, 4.35%
Materials Today Sustainability
1 публикация, 4.35%
Helvetica Chimica Acta
1 публикация, 4.35%
European Journal of Organic Chemistry
1 публикация, 4.35%
Journal of Heterocyclic Chemistry
1 публикация, 4.35%
Macromolecular Rapid Communications
1 публикация, 4.35%
Journal of the American Chemical Society
1 публикация, 4.35%
Journal of Organic Chemistry
1 публикация, 4.35%
Organometallics
1 публикация, 4.35%
Journal of Materials Chemistry C
1 публикация, 4.35%
Progress in Heterocyclic Chemistry
1 публикация, 4.35%
Russian Chemical Reviews
1 публикация, 4.35%
Batteries & Supercaps
1 публикация, 4.35%
1
2
3

Издатели

1
2
3
4
5
6
7
8
Wiley
8 публикаций, 34.78%
Royal Society of Chemistry (RSC)
6 публикаций, 26.09%
Elsevier
5 публикаций, 21.74%
American Chemical Society (ACS)
3 публикации, 13.04%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 4.35%
1
2
3
4
5
6
7
8
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
23
Поделиться
Цитировать
ГОСТ |
Цитировать
Díaz M. C. et al. Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers // Journal of Organic Chemistry. 2004. Vol. 69. No. 13. pp. 4492-4499.
ГОСТ со всеми авторами (до 50) Скопировать
Díaz M. C., Illescas B. M., Seoane C., Martin N. Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers // Journal of Organic Chemistry. 2004. Vol. 69. No. 13. pp. 4492-4499.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/jo049741z
UR - https://doi.org/10.1021/jo049741z
TI - Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers
T2 - Journal of Organic Chemistry
AU - Díaz, Marta C
AU - Illescas, Beatriz M.
AU - Seoane, Carlos
AU - Martin, Nazario
PY - 2004
DA - 2004/06/01
PB - American Chemical Society (ACS)
SP - 4492-4499
IS - 13
VL - 69
PMID - 15202907
SN - 0022-3263
SN - 1520-6904
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2004_Díaz,
author = {Marta C Díaz and Beatriz M. Illescas and Carlos Seoane and Nazario Martin},
title = {Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers},
journal = {Journal of Organic Chemistry},
year = {2004},
volume = {69},
publisher = {American Chemical Society (ACS)},
month = {jun},
url = {https://doi.org/10.1021/jo049741z},
number = {13},
pages = {4492--4499},
doi = {10.1021/jo049741z}
}
MLA
Цитировать
Díaz, Marta C., et al. “Synthesis and Electron-Donor Ability of the First Conjugated π-Extended Tetrathiafulvalene Dimers.” Journal of Organic Chemistry, vol. 69, no. 13, Jun. 2004, pp. 4492-4499. https://doi.org/10.1021/jo049741z.