Double-C,N-chelated tri- and diorganotin(IV) fluorides
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F05%3A00002968" target="_blank" >RIV/00216275:25310/05:00002968 - isvavai.cz</a>
Alternative codes found
RIV/61389013:_____/05:00029540 RIV/00216208:11310/05:00008391 RIV/00216208:11310/05:8391
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Double-C,N-chelated tri- and diorganotin(IV) fluorides
Original language description
Attempts to fluorinate the compounds (L-CN)(SnPhCl)-Sn-2 (1), (L-CN)(2)SnCl2 (2), (L-CN)(2)SnBr2 (3), (L-CN)(2)SnI2 (4) and (LSnPhCl2)-Sn-CN (5), where LCN is {2-[(CH3)(2)NCH2]C6H4}(-), were made by four different methods. The fluorinated monomeric five-coordinated analogue of 1 was made by fluorination of I with KF/18-crown-6 ether and by metathetical fluorination with 10 ((LSnBu2F)-Sn-CN). The fluorinated monomeric six-coordinated analogue ((L-CN)(2)SnF2(7)) of diorganotin compounds 2-4 was made easily by all methods used in adequate yield. The fluorination of 5 by all methods did not lead to the monomeric product and phenyl group migrations were observed during the course of these reactions. The most clear is the reaction of 5 with two equivalents of 10 leading to, presumably, a fluorinated analogue of 5 having a trimeric structure, which reacts immediately with three equivalents of NH4F in methanol to give the complex compound NH4+[(LPhSnF3)-Ph-CN](-) in quantitative yield. Compoun
Czech name
Double-C,N-chelated tri- and diorganotin(IV) fluorides
Czech description
Attempts to fluorinate the compounds (L-CN)(SnPhCl)-Sn-2 (1), (L-CN)(2)SnCl2 (2), (L-CN)(2)SnBr2 (3), (L-CN)(2)SnI2 (4) and (LSnPhCl2)-Sn-CN (5), where LCN is {2-[(CH3)(2)NCH2]C6H4}(-), were made by four different methods. The fluorinated monomeric five-coordinated analogue of 1 was made by fluorination of I with KF/18-crown-6 ether and by metathetical fluorination with 10 ((LSnBu2F)-Sn-CN). The fluorinated monomeric six-coordinated analogue ((L-CN)(2)SnF2(7)) of diorganotin compounds 2-4 was made easily by all methods used in adequate yield. The fluorination of 5 by all methods did not lead to the monomeric product and phenyl group migrations were observed during the course of these reactions. The most clear is the reaction of 5 with two equivalents of 10 leading to, presumably, a fluorinated analogue of 5 having a trimeric structure, which reacts immediately with three equivalents of NH4F in methanol to give the complex compound NH4+[(LPhSnF3)-Ph-CN](-) in quantitative yield. Compoun
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CA - Inorganic chemistry
OECD FORD branch
—
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2005
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
JOURNAL OF FLUORINE CHEMISTRY
ISSN
0022-1139
e-ISSN
—
Volume of the periodical
—
Issue of the periodical within the volume
126
Country of publishing house
NL - THE KINGDOM OF THE NETHERLANDS
Number of pages
9
Pages from-to
1531-1538
UT code for WoS article
—
EID of the result in the Scopus database
—