Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Ignacio Vargas-Baca"'
Autor:
Peter C. Ho, Patrick Szydlowski, Jocelyn Sinclair, Philip J. W. Elder, Joachim Kübel, Chris Gendy, Lucia Myongwon Lee, Hilary Jenkins, James F. Britten, Derek R. Morim, Ignacio Vargas-Baca
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-10 (2016)
Similarly to halogen bonding, the heavier chalcogens are capable of forming supramolecular links with electron rich sites. Here, the authors show that these forces can allow the formation of well-defined cyclic structures that are stable in solution
Externí odkaz:
https://doaj.org/article/cf1ebf0553e54ae4936f6e679632a9a1
Autor:
Nicholas R. Andreychuk, Balamurugan Vidjayacoumar, Jeffrey S. Price, Sophie Kervazo, Craig A. Peeples, David J. H. Emslie, Valérie Vallet, André S. P. Gomes, Florent Réal, Georg Schreckenbach, Paul W. Ayers, Ignacio Vargas-Baca, Hilary A. Jenkins, James F. Britten
Publikováno v:
Chemical Science
Chemical Science, 2022, 13, pp.13748-13763. ⟨10.1039/D2SC04302E⟩
Chemical Science, 2022, 13, pp.13748-13763. ⟨10.1039/D2SC04302E⟩
International audience; Reaction of [(XA2)U(CH2SiMe3)2] (1; XA2 = 4,5-bis(2,6-diisopropylanilido)-2,7-di-tert-butyl-9,9- dimethylxanthene) with 1 equivalent of [Ph3C][B(C6F5)4] in arene solvents afforded the arene-coordinated uranium alkyl cations, [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53fb3129a1422e8a56026912cc229467
https://doi.org/10.1039/d2sc04302e
https://doi.org/10.1039/d2sc04302e
Publikováno v:
Chalcogen Chemistry: Fundamentals and Applications ISBN: 9781839164224
The past two decades have witnessed a significant growth of interest in supramolecular interactions in which a group-16 atom acts as an electrophilic centre. This chapter provides an overview of the uses of chalcogen bonding interactions in supramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d22f048f251874eaf1e5064d28027ad
https://doi.org/10.1039/bk9781839167386-00494
https://doi.org/10.1039/bk9781839167386-00494
Publikováno v:
Inorganic Chemistry. 60:16726-16733
Formal substitution of the oxygen atom of an iso-tellurazole N-oxide with deprotonated (ortho, meta, and para)-hydroxyphenyl groups generated molecules that readily aggregate through Te···O chalcogen bonding (ChB) interactions. The molecules under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3935cdf895b416a1d06872a84fbd9f29
https://doi.org/10.1021/acs.inorgchem.1c02585
https://doi.org/10.1021/acs.inorgchem.1c02585
Autor:
Anton I. Smolentsev, Jens Beckmann, Alexey A. Dmitriev, Nina P. Gritsan, Ignacio Vargas-Baca, Andrey V. Zibarev, Nikolay A. Puskarevsky
Publikováno v:
Chemical Communications. 56:1113-1116
Reduction of 2,1,3-benzotelluradiazole (3) yielded a crystalline solid that features a trimeric dianion formally composed of two [3]˙− and one 3 bridged by unusually asymmetric Te⋯N chalcogen bonds. The solid is diamagnetic due to strong antifer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8a7c50e1045e1cd5e84077e45adf24
https://doi.org/10.1039/c9cc08110k
https://doi.org/10.1039/c9cc08110k
Publikováno v:
Inorganic chemistry. 60(21)
Formal substitution of the oxygen atom of an iso-tellurazole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b89c81866f4cdbc82fd87781af3b4de
https://pubmed.ncbi.nlm.nih.gov/34672560
https://pubmed.ncbi.nlm.nih.gov/34672560
Autor:
Faisal Adam Pani, Hilary A. Jenkins, Ignacio Vargas-Baca, Victoria B. Corless, James F. Britten, Allan He, Lucia Myongwon Lee, Helen Luu
Publikováno v:
Dalton Transactions. 48:12541-12548
The synthesis, and spectroscopic and structural characterization of bridged dicationic derivatives of benzo-2,1,3-selenadiazoles are reported. The chloride salt of [H4C6NSeN–CH2–CH2–NSeNC6H4]2+ crystallizes forming a macrocyclic structure in wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::261349396a6bb307b7e5a1efc5811de1
https://doi.org/10.1039/c9dt02311a
https://doi.org/10.1039/c9dt02311a
Autor:
Peter C. Ho, Shanel Sequeira, Alberto Cevallos, Robert Bui, James F. Britten, Ignacio Vargas-Baca
Publikováno v:
Dalton Transactions. 48:4879-4886
Pt(ii) and Rh(iii) readily form complexes with 3-methyl-5-aryl-1,2-tellurazole 2-oxides (L = (3-Me-5-Ar-1,2-C3HTe(NO)). The aryl group is either phenyl or 3,5-di-tert-butylphenyl, the latter case being a new derivative with enhanced solubility. The c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8c0215cf517c2bd81bb44cd652ecae4
https://doi.org/10.1039/c9dt00500e
https://doi.org/10.1039/c9dt00500e
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(42)
Chlorination of 3-methyl-5-phenyl-1,2-tellurazole-2-oxide yielded the λ4 Te dichloro derivative. Its crystal structure demonstrates that the heterocycle retains its ability to autoassociate by chalcogen bonding (ChB) forming macrocyclic tetramers. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fd3b43cdc9e78be4da4b0533cb07741
https://pubmed.ncbi.nlm.nih.gov/34018275
https://pubmed.ncbi.nlm.nih.gov/34018275
Publikováno v:
Organometallics. 37:3010-3023
Wilkinson’s manganese(I) ethylene hydride complex trans-[(dmpe)2MnH(C2H4)] (1) reacts as a source of a low-coordinate manganese(I) ethyl complex. This is illustrated in the reactivity of 1 toward a variety of reagents. Reactions of 1 with primary s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7175d9193226b895104a9cfcd6cca7a6
https://doi.org/10.1021/acs.organomet.8b00379
https://doi.org/10.1021/acs.organomet.8b00379