Antimony centre in three different roles: does donor strength or acceptor ability determine the bonding pattern?
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F24%3A39922153" target="_blank" >RIV/00216275:25310/24:39922153 - isvavai.cz</a>
Výsledek na webu
<a href="https://pubs.rsc.org/en/Content/ArticleLanding/2024/DT/D4DT02787F" target="_blank" >https://pubs.rsc.org/en/Content/ArticleLanding/2024/DT/D4DT02787F</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/d4dt02787f" target="_blank" >10.1039/d4dt02787f</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Antimony centre in three different roles: does donor strength or acceptor ability determine the bonding pattern?
Popis výsledku v původním jazyce
A set of antimony(iii) compounds containing a ligand (Ar) with a pendant guanidine function (where Ar = 2-[(Me2N)2C 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 N]C6H4) was prepared and characterized. This includes triorgano-Ar3Sb, diorgano-Ar2SbCl and monoorgano-ArSbCl2 compounds and they were characterized by 1H and 13C NMR spectroscopy and by single-crystal X-ray diffraction analysis (sc-XRD). The coordination capability of Ar3Sb and Ar2SbCl was examined in the reactions with either cis-[PdCl2(CH3CN)2] or PtCl2 and complexes cis-[(kappa 2-Sb,N-Ar3Sb)MCl2] (M = Pd 1, Pt 2) and [(kappa 3-N,Sb,N-Ar2SbCl)MCl2] (M = Pd 3, Pt 4) were isolated, while their structures were determined by sc-XRD. Notably, the ligands Ar3Sb and Ar2SbCl exhibit different coordination modes - bidentate and tridentate, respectively - and the antimony exhibits three distinct bonding modes in complexes 1-4, which were also subjected to theoretical studies. The guanidine substituted organostibines allowed remarkable coordination variability including three distinct modes of M & ctdot;Sb bonding (M = Pd or Pt), i.e. Sb -> M L-type and Z-type interactions involving M <- Sb donation and M -> Sb backdonation.
Název v anglickém jazyce
Antimony centre in three different roles: does donor strength or acceptor ability determine the bonding pattern?
Popis výsledku anglicky
A set of antimony(iii) compounds containing a ligand (Ar) with a pendant guanidine function (where Ar = 2-[(Me2N)2C 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 N]C6H4) was prepared and characterized. This includes triorgano-Ar3Sb, diorgano-Ar2SbCl and monoorgano-ArSbCl2 compounds and they were characterized by 1H and 13C NMR spectroscopy and by single-crystal X-ray diffraction analysis (sc-XRD). The coordination capability of Ar3Sb and Ar2SbCl was examined in the reactions with either cis-[PdCl2(CH3CN)2] or PtCl2 and complexes cis-[(kappa 2-Sb,N-Ar3Sb)MCl2] (M = Pd 1, Pt 2) and [(kappa 3-N,Sb,N-Ar2SbCl)MCl2] (M = Pd 3, Pt 4) were isolated, while their structures were determined by sc-XRD. Notably, the ligands Ar3Sb and Ar2SbCl exhibit different coordination modes - bidentate and tridentate, respectively - and the antimony exhibits three distinct bonding modes in complexes 1-4, which were also subjected to theoretical studies. The guanidine substituted organostibines allowed remarkable coordination variability including three distinct modes of M & ctdot;Sb bonding (M = Pd or Pt), i.e. Sb -> M L-type and Z-type interactions involving M <- Sb donation and M -> Sb backdonation.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10300 - Physical sciences
Návaznosti výsledku
Projekt
<a href="/cs/project/GA21-02964S" target="_blank" >GA21-02964S: Dusíkaté ligandy pro prvky nepřechodných kovů - objemnější, konjugovanější a reaktivnější</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2024
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Dalton Transactions
ISSN
1477-9226
e-ISSN
1477-9234
Svazek periodika
53
Číslo periodika v rámci svazku
43
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
6
Strana od-do
17721-17726
Kód UT WoS článku
001335205900001
EID výsledku v databázi Scopus
2-s2.0-85207367453