Half-pseudoferrocene cations from nucleophilic addition of o-carboranyl anions to the [(eta(6)-mesitylene)(2)Fe](2+) dication

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F12%3A00382801" target="_blank" >RIV/61388980:_____/12:00382801 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1039/c2dt30181d" target="_blank" >http://dx.doi.org/10.1039/c2dt30181d</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c2dt30181d" target="_blank" >10.1039/c2dt30181d</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Half-pseudoferrocene cations from nucleophilic addition of o-carboranyl anions to the [(eta(6)-mesitylene)(2)Fe](2+) dication

Popis výsledku v původním jazyce

Reactions between the mesitylene (mes) dication [(eta(6)-mes)(2)Fe](2+) (1a) [(PF6-)(2) salt] and lithium o-carboranes Li[1-R-1,2-C2B10H11] (2) (R = H, 2a; Me, 2b; Ph, 2c) at low temperature (-60 degrees C, 1 h, followed by stirring for 2 h at r.t.) in THF resulted in a clean addition of the corresponding carborane anions to one of the unsubstituted arene sites in 1a, forming a series of orange monocations of general structure [(eta(5)-mes-exo-6-{2-R-1,2-C2B10H11})Fe(eta(6)-mes)]+ (3) (R = H, 3a; Me, 3b; Ph, 3c) which were isolated as PF6- salts (3PF(6)) in yields ranging 50-75%. Individual complexes were obtained on purification by LC or preparative TLC on a silica gel substrate, using MeCN-CH2Cl2 mixtures as the mobile phase. Interestingly, the room-temperature reaction between 2a (threefold excess) and 1a(PF6)(2) with a reverse order of addition of the reaction components yielded an orange salt [(eta(5)-mes-exo-6-{1,2-C2B10H11}) Fe(eta(6)-mes)](+)[closo-nido-H11B10C2-C2B10H12](-) (3

Název v anglickém jazyce

Half-pseudoferrocene cations from nucleophilic addition of o-carboranyl anions to the [(eta(6)-mesitylene)(2)Fe](2+) dication

Popis výsledku anglicky

Reactions between the mesitylene (mes) dication [(eta(6)-mes)(2)Fe](2+) (1a) [(PF6-)(2) salt] and lithium o-carboranes Li[1-R-1,2-C2B10H11] (2) (R = H, 2a; Me, 2b; Ph, 2c) at low temperature (-60 degrees C, 1 h, followed by stirring for 2 h at r.t.) in THF resulted in a clean addition of the corresponding carborane anions to one of the unsubstituted arene sites in 1a, forming a series of orange monocations of general structure [(eta(5)-mes-exo-6-{2-R-1,2-C2B10H11})Fe(eta(6)-mes)]+ (3) (R = H, 3a; Me, 3b; Ph, 3c) which were isolated as PF6- salts (3PF(6)) in yields ranging 50-75%. Individual complexes were obtained on purification by LC or preparative TLC on a silica gel substrate, using MeCN-CH2Cl2 mixtures as the mobile phase. Interestingly, the room-temperature reaction between 2a (threefold excess) and 1a(PF6)(2) with a reverse order of addition of the reaction components yielded an orange salt [(eta(5)-mes-exo-6-{1,2-C2B10H11}) Fe(eta(6)-mes)](+)[closo-nido-H11B10C2-C2B10H12](-) (3

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CA - Anorganická chemie

OECD FORD obor

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Projekt

<a href="/cs/project/GAP207%2F11%2F0705" target="_blank" >GAP207/11/0705: Arenové komplexy železa modikované karborany</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2012

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Dalton Transactions

ISSN

1477-9226

e-ISSN

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Svazek periodika

41

Číslo periodika v rámci svazku

23

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

5

Strana od-do

7151-7155

Kód UT WoS článku

000304487400034

EID výsledku v databázi Scopus

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