Electrochemical and Reactivity Studies of N→Sn Coordinated Distannynes
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F18%3A39913496" target="_blank" >RIV/00216275:25310/18:39913496 - isvavai.cz</a>
Výsledek na webu
<a href="http://dx.doi.org/10.1002/chem.201703960" target="_blank" >http://dx.doi.org/10.1002/chem.201703960</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/chem.201703960" target="_blank" >10.1002/chem.201703960</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Electrochemical and Reactivity Studies of N→Sn Coordinated Distannynes
Popis výsledku v původním jazyce
Studies are focused on the redox potentials of N -> Sn coordinated distannnynes {L1-3Sn}(2) (L-1 = 1, L-2 = 2 and L-3 = 3, in which L-1 is [C6H3-2,6-(Me2NCH2)(2)](-), L-2 is [C6H2-2,4-tBu(2)-6-(Et2NCH2)](-) and L-3 is [C6H2-2,4-tBu(2)-6-(DippN=CH)](-); Dipp = 2,6-diisopropylphenyl), containing the tin atom in oxidation state + I. Distannynes 1-3 were used as ligands for transition metals, and complexes [{(LSn)-Sn-1}(2)center dot Fe(CO)(4)] (4) and [{(LSn)-Sn-2}(2)center dot Fe(CO)(4)] (5) were prepared. The set of N -> Sn coordinated distannynes 1-5 was studied by cyclic voltammetry measurements and the oxidation potentials of tin atoms in 1-5 were determined. The redox potentials are influenced by either ligands L1-3 or Sn-I -> Fe coordination. Oxidation reactions of 1-3 were also studied. The reaction of 2 with (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) provided mixed organotin oxide {((LSnO)-Sn-2)(L-2) Sn(mu-O)}(2) (6) as a consequence of the instability of the expected {(LSn)-Sn-2 center dot TEMPO} complex. To support this proposed mechanism, the N -> Ge coordinated digermyne {(LGe)-Ge-2}(2) (7) was prepared. The reaction of 7 with TEMPO provided the expected complex {(LGe)-Ge-2 center dot TEMPO} (8).
Název v anglickém jazyce
Electrochemical and Reactivity Studies of N→Sn Coordinated Distannynes
Popis výsledku anglicky
Studies are focused on the redox potentials of N -> Sn coordinated distannnynes {L1-3Sn}(2) (L-1 = 1, L-2 = 2 and L-3 = 3, in which L-1 is [C6H3-2,6-(Me2NCH2)(2)](-), L-2 is [C6H2-2,4-tBu(2)-6-(Et2NCH2)](-) and L-3 is [C6H2-2,4-tBu(2)-6-(DippN=CH)](-); Dipp = 2,6-diisopropylphenyl), containing the tin atom in oxidation state + I. Distannynes 1-3 were used as ligands for transition metals, and complexes [{(LSn)-Sn-1}(2)center dot Fe(CO)(4)] (4) and [{(LSn)-Sn-2}(2)center dot Fe(CO)(4)] (5) were prepared. The set of N -> Sn coordinated distannynes 1-5 was studied by cyclic voltammetry measurements and the oxidation potentials of tin atoms in 1-5 were determined. The redox potentials are influenced by either ligands L1-3 or Sn-I -> Fe coordination. Oxidation reactions of 1-3 were also studied. The reaction of 2 with (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) provided mixed organotin oxide {((LSnO)-Sn-2)(L-2) Sn(mu-O)}(2) (6) as a consequence of the instability of the expected {(LSn)-Sn-2 center dot TEMPO} complex. To support this proposed mechanism, the N -> Ge coordinated digermyne {(LGe)-Ge-2}(2) (7) was prepared. The reaction of 7 with TEMPO provided the expected complex {(LGe)-Ge-2 center dot TEMPO} (8).
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10402 - Inorganic and nuclear chemistry
Návaznosti výsledku
Projekt
<a href="/cs/project/LM2015082" target="_blank" >LM2015082: Centrum materiálů a nanotechnologií</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Chemistry - A European Journal
ISSN
0947-6539
e-ISSN
—
Svazek periodika
24
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
DE - Spolková republika Německo
Počet stran výsledku
8
Strana od-do
1104-1111
Kód UT WoS článku
000427316700018
EID výsledku v databázi Scopus
2-s2.0-85038033404