A 1:2 reaction of Ph3SnOSnPh3 1 with RfCOOH 2 leads to the formation of [Ph2Sn(OH)OC(O)(Rf)]2 3, by means of a facile Sn-C bond cleavage process.
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http://dx.doi.org/10.1039/b212409b | DOI Listing |
Acta Crystallogr E Crystallogr Commun
September 2024
The title compound, [Sn(CH)Cl(CHN)], which was obtained by the reaction between 1,10-phenanthroline and phenyl-tin trichloride in methanol, exhibits intra-molecular hydrogen-bonding inter-actions involving the chlorine and hydrogen atoms. Crystal cohesion is ensured by inter-molecular C-H⋯Cl hydrogen bonds, as well as -⋯π and π-stacking inter-actions involving three different aromatic rings with centroid-centroid distances of 3.6605 (13), 3.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian, 350002, P. R. China.
Chem Commun (Camb)
November 2023
Department of Chemistry, University of California, One Shields Avenue, Davis, 95616, USA.
Thermal Sn-C cleavage in the diarylstannylene Sn(Ar) (Ar = CH-2,6-(CH-2,6-iPr)) was used to generate ˙Sn(Ar) and ˙Ar radicals for alkyne arylstannylation. The radical pair and RCCR' (R = H, R' = Ph; R = Ph, R' = Ph; R = H, R' = CH; R = H, R' = SiMe) in refluxing benzene generate the aryl vinyl stannylene complexes, ArSn{C(CH)-C(H)(Ar)} (1), ArSn{C(CH)-C(H)(CH)} (2) and ArSn{C(CH)-C(H)(Ar)} (3) respectively. For HCCSiMe, the known distannene {Sn(CCSiMe)Ar} (4) was also generated from this new method.
View Article and Find Full Text PDFJ Am Chem Soc
March 2023
Innovation Center for Chemical Sciences, Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.
Due to their intrinsic high reactivity, isolation of heavier analogues of carbynes remains a great challenge. Here, we report the synthesis and characterization of a neutral monosubstituted Sn(I) radical () supported by a sterically hindered hydrindacene ligand, which represents the first tin analogue of a free carbyne. Different from all Sn(I/III) species reported thus far, the presence of a sole Sn-C σ bond in renders the remaining two Sn 5p orbitals energetically almost degenerate, of which one is singly occupied and the other is empty.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
January 2023
Laboratoire de Chimie Minérale et Analytique (LACHIMIA), Département de Chimie, Faculté des Sciences et Techniques, Université Cheikh Anta Diop, Dakar, Senegal.
The title Sn complex, [Sn(CH)Cl(CHOP)], is a formal adduct between triphenyl phosphate (PhO)P=O and the stannane derivative chlorido-tri-phenyl-tin, SnPhCl. The structure refinement reveals that this mol-ecule displays the largest Sn-O bond length for compounds including the =O→SnPhCl fragment ( = P, S, C, or V), 2.6644 (17) Å.
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