Home / Publications / First examples of a covalent bond between gold and selenophene

First examples of a covalent bond between gold and selenophene

Alla Petrenko 1
Alla Petrenko
Sergey Belyakov 1
Sergey Belyakov
Pavel Arsenyan 1
Pavel Arsenyan
Published 2020-08-31
CommunicationVolume 30, Issue 5, 572-573
1
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Petrenko A., Belyakov S., Arsenyan P. First examples of a covalent bond between gold and selenophene // Mendeleev Communications. 2020. Vol. 30. No. 5. pp. 572-573.
GOST all authors (up to 50) Copy
Petrenko A., Belyakov S., Arsenyan P. First examples of a covalent bond between gold and selenophene // Mendeleev Communications. 2020. Vol. 30. No. 5. pp. 572-573.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2020.09.006
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.09.006
TI - First examples of a covalent bond between gold and selenophene
T2 - Mendeleev Communications
AU - Petrenko, Alla
AU - Belyakov, Sergey
AU - Arsenyan, Pavel
PY - 2020
DA - 2020/08/31
PB - Mendeleev Communications
SP - 572-573
IS - 5
VL - 30
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2020_Petrenko,
author = {Alla Petrenko and Sergey Belyakov and Pavel Arsenyan},
title = {First examples of a covalent bond between gold and selenophene},
journal = {Mendeleev Communications},
year = {2020},
volume = {30},
publisher = {Mendeleev Communications},
month = {Aug},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.09.006},
number = {5},
pages = {572--573},
doi = {10.1016/j.mencom.2020.09.006}
}
MLA
Cite this
MLA Copy
Petrenko, Alla, et al. “First examples of a covalent bond between gold and selenophene.” Mendeleev Communications, vol. 30, no. 5, Aug. 2020, pp. 572-573. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.09.006.

Keywords

gold compounds
organogold compounds
organoselenium compounds
selenophenes
X-ray

Abstract

2(3)-Dichloroauryl-3(2)-(pyridin-2-yl)benzo[b]selenophenes bearing covalent bond with gold(iii) were synthesized by the treatment of (pyridin-2-yl)benzoselenophenes with sodium tetrachloroaurate. Molecular structures were unambiguously confirmed by X-ray analysis.

References

1.
Gold(III) Complexes for Antitumor Applications: An Overview
Bertrand B., Williams M.R., Bochmann M.
Chemistry - A European Journal, 2018
3.
Cyclometalated Au III Complexes for Cysteine Arylation in Zinc Finger Protein Domains: towards Controlled Reductive Elimination
Wenzel M.N., Bonsignore R., Thomas S.R., Bourissou D., Barone G., Casini A.
Chemistry - A European Journal, 2019
4.
Luminescent Gold(I) Complexes of 1-Pyridyl-3-anthracenylchalcone Inducing Apoptosis in Colon Carcinoma Cells and Antivascular Effects
González J.J., Ortega E., Rothemund M., Gold M., Vicente C., de Haro C., Bautista D., Schobert R., Ruiz J.
Inorganic Chemistry, 2019
5.
Development of Catalysts and Ligands for Enantioselective Gold Catalysis
Wang Y., Lackner A.D., Toste F.D.
Accounts of Chemical Research, 2013
6.
Ligand Effects in Homogeneous Au Catalysis
Gorin D.J., Sherry B.D., Toste F.D.
Chemical Reviews, 2008
7.
Gold-Catalyzed Cycloisomerizations of Enynes: A Mechanistic Perspective
Jiménez-Núñez E., Echavarren A.M.
Chemical Reviews, 2008
8.
Gold-Catalyzed Organic Transformations
Li Z., Brouwer C., He C.
Chemical Reviews, 2008
9.
Yakushkin S.S., Nuzhdin A.L., Artiukha E.A., Plyusnin P.E., Bukhtiyarova G.A., Martyanov O.N.
Mendeleev Communications, 2018
10.
Gold and silver nanoparticle-catalyzed synthesis of heterocyclic compounds
Kaur R., Bariwal J., Voskressensky L.G., Van der Eycken E.V.
Chemistry of Heterocyclic Compounds, 2018
11.
Luminescent Organometallic Nanomaterials with Aggregation-Induced Emission
Shu T., Wang J., Su L., Zhang X.
Critical Reviews in Analytical Chemistry, 2018
12.
Luminescent phosphine gold(I) alkynyl complexes. Highlights from 2010 to 2018
13.
Semenova A.A., Tarasov A.B., Goodilin E.A.
Mendeleev Communications, 2019
14.
Aurophilicity and Photoluminescence of (6‐Diphenylpnicogenoacenaphth‐5‐yl)gold Compounds
Do T.G., Hupf E., Lork E., Kögel J.F., Mohr F., Brown A., Toyoda R., Sakamoto R., Nishihara H., Mebs S., Beckmann J.
European Journal of Inorganic Chemistry, 2019
15.
2,6-Diphenylbenzo[1,2-b:4,5-b‘]dichalcogenophenes:  A New Class of High-Performance Semiconductors for Organic Field-Effect Transistors
Takimiya K., Kunugi Y., Konda Y., Niihara N., Otsubo T.
Journal of the American Chemical Society, 2004
16.
Arsenyan P., Vasiljeva J., Belyakov S.
Mendeleev Communications, 2014
17.
Triplet Tellurophene-Based Acceptors for Organic Solar Cells
Yang L., Gu W., Lv L., Chen Y., Yang Y., Ye P., Wu J., Hong L., Peng A., Huang H.
Angewandte Chemie - International Edition, 2018
18.
Thiophene, Selenophene, and Tellurophene-based Three-Dimensional Organic Frameworks
Li P., Schon T.B., Seferos D.S.
Angewandte Chemie - International Edition, 2015
19.
Chulanova E.A., Semenov N.A., Pushkarevsky N.A., Gritsan N.P., Zibarev A.V.
Mendeleev Communications, 2018
20.
Efficient p-phenylene based OLEDs with mixed interfacial exciplex emission
Data P., Motyka R., Lapkowski M., Suwinski J., Jursenas S., Kreiza G., Miasojedovas A., Monkman A.P.
Electrochimica Acta, 2015
21.
Red fluorescent siloles with aggregation-enhanced emission characteristics
Chen B., Nie H., Hu R., Qin A., Zhao Z., Tang B.
Science China Chemistry, 2016
22.
Multipurpose selenophene containing conjugated polymers for optoelectronic applications
Onk I., Hizalan G., Cevher S.C., Hacioglu S.O., Toppare L., Cirpan A.
Journal of Macromolecular Science - Pure and Applied Chemistry, 2017
23.
Synthesis of fused chalcogenophenocarbazoles: towards dual emission resulting from hybridized local and charge-transfer states
Petrenko A., Bezvikonnyi O., Volyniuk D., Danyliv Y., Simokaitiene J., Belyakov S., Grazulevicius J.V., Arsenyan P.
New Journal of Chemistry, 2020
24.
Synthesis and Performance in OLEDs of Selenium-Containing Phosphorescent Emitters with Red Emission Color Deeper Than the Corresponding NTSC Standard.
Arsenyan P., Petrenko A., Leitonas K., Volyniuk D., Simokaitiene J., Klinavičius T., Skuodis E., Lee J., Gražulevičius J.V.
Inorganic Chemistry, 2019
25.
Benzoselenophenylpyridine platinum complexes: green versus red phosphorescence towards hybrid OLEDs
Petrenko A., Leitonas K., Volyniuk D., Baryshnikov G.V., Belyakov S., Minaev B.F., Ågren H., Durgaryan H., Gražulevičius J.V., Arsenyan P.
Dalton Transactions, 2020
27.
Suzuki–Miyaura coupling of arylboronic acids to gold(iii)
Maity A., Sulicz A.N., Deligonul N., Zeller M., Hunter A.D., Gray T.G.
Chemical Science, 2015
28.
Geminally Diaurated Gold(I) Aryls from Boronic Acids
Heckler J.E., Zeller M., Hunter A.D., Gray T.G.
Angewandte Chemie - International Edition, 2012