Germylenes and stannylenes stabilized within N2PE rings (E = Ge or Sn): combined experimental and theoretical study
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F16%3A39902107" target="_blank" >RIV/00216275:25310/16:39902107 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1039/c6dt01616b" target="_blank" >http://dx.doi.org/10.1039/c6dt01616b</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1039/c6dt01616b" target="_blank" >10.1039/c6dt01616b</a>
Alternative languages
Result language
angličtina
Original language name
Germylenes and stannylenes stabilized within N2PE rings (E = Ge or Sn): combined experimental and theoretical study
Original language description
The deprotonation of aminophosphanes PhP(NHR)(2) (R = t-Bu or Dip; Dip = 2,6-i-Pr2C6H3) and t-BuP (NHDip)(2) using n-BuLi gave, depending on the stoichiometry, both the dilithium compounds {[PhP(Nt-Bu) (2)]Li-2}(2) (1), [PhP(Nt-Bu)(NDip)]Li-2 center dot(Et2O) (3), [t-BuP(NDip)(2)]Li-2 center dot(Et2O)(2) (5) and [t-BuP(NDip)(2)]Li-2 center dot(tmeda)(2) (5a), and the monolithium compounds [PhP(NHt-Bu)(NR)]Li center dot(tmeda) (R = t-Bu 2, Dip 4) and [t-BuP (NHDip)(NDip)]Li center dot(tmeda) (6). Treatment of 1, 3 and 5 with GeCl2 center dot dioxane or SnCl2 in a 1 : 1 stoichiometric ratio gave the corresponding tetrylenes [PhP(Nt-Bu)(2)] E (E = Ge 7, Sn 10), [PhP(Nt-Bu)(NDip)] Ge (8) and [t-BuP(NDip)(2)] E (E = Ge 9, Sn 11). The heteroleptic germylene [Ph(H)P(Nt-Bu)(2)] GeCl (12) was obtained by the reaction of the monolithium compound [PhP(NHt-Bu)(Nt-Bu)]Li center dot(tmeda) (2) with GeCl2 center dot dioxane in a 1 : 1 stoichiometric ratio, as a result of a spontaneous NH -> PH tautomeric shift in the ligand backbone. In contrast, an analogous reaction with SnCl2 produced only stannylene 10 along with the PhP(NHt-Bu)(2) starting material, suggesting scrambling of the ligands rather than a NH -> PH tautomeric shift. Finally, heating 5a in solution led to P-C bond cleavage and formation of the bis(imino) phosphide [DipNPNDip] Li center dot(tmeda) (13). The reaction of 13 with GeCl2 center dot dioxane, SnCl2 or PbCl2 in a 2 : 1 stoichiometric ratio yielded the unprecedented tetrylenes [DipNPNDip](2)E (E = Ge 14, Sn 15 and Pb 16), in which the tetrylene center is incorporated within two N2PE rings. Treatment of the monolithium compound 2 with n-BuLi and K (or KC8) gave [t-BuNPNt-Bu]Li center dot(tmeda) (17) and{[t-BuNPNt-Bu] K(tmeda)}(2) (18), respectively.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CA - Inorganic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GAP207%2F12%2F0223" target="_blank" >GAP207/12/0223: Hybrid ligands for low valent metal centres stabilization/specific activation.</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Dalton Transactions
ISSN
1477-9226
e-ISSN
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Volume of the periodical
45
Issue of the periodical within the volume
25
Country of publishing house
GB - UNITED KINGDOM
Number of pages
12
Pages from-to
10343-10354
UT code for WoS article
000378392200029
EID of the result in the Scopus database
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