4098-97-9Relevant articles and documents
Silane bridging luminescent material, preparation method and application thereof, and color developing agent
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Paragraph 0067; 0071-0073, (2020/07/13)
The invention relates to the technical field of detection, and discloses a silane bridging luminescent material, a preparation method and an application thereof, and a color developing agent, the silane bridging luminescent material has a structure repres
Conductive molecular silicon
Klausen, Rebekka S.,Widawsky, Jonathan R.,Steigerwald, Michael L.,Venkataraman, Latha,Nuckolls, Colin
supporting information; experimental part, p. 4541 - 4544 (2012/04/23)
Bulk silicon, the bedrock of information technology, consists of the deceptively simple electronic structure of just Si-Si σ bonds. Diamond has the same lattice structure as silicon, yet the two materials have dramatically different electronic properties. Here we report the specific synthesis and electrical characterization of a class of molecules, oligosilanes, that contain strongly interacting Si-Si σ bonds, the essential components of the bulk semiconductor. We used the scanning tunneling microscope-based break-junction technique to compare the single-molecule conductance of these oligosilanes to those of alkanes. We found that the molecular conductance decreases exponentially with increasing chain length with a decay constant β = 0.27 ± 0.01 A-1, comparable to that of a conjugated chain of C = C π bonds. This result demonstrates the profound implications of σ conjugation for the conductivity of silicon.
The preparation and analysis of the phenyldimethylsilyllithium reagent and its reaction with silyl enol ethers
Fleming, Ian,Roberts, Richard S.,Smith, Stephen C.
, p. 1209 - 1214 (2007/10/03)
Phenyldimethylsilyllithium is formed from lithium and phenyldimethylsilyl chloride by slow cleavage of the Si-Si bond of 1,1,2,2-tetramethyl-1,2-diphenyldisilane after the rapid formation of the disilane. 1,1,2,2-Tetramethyl-1,2-diphenyldisiloxane, produced from the silyl chloride by reaction with oxides and hydroxides on the lithium metal surface, is cleaved by dimethyl(phenyl)silyllithium to give lithium dimethyl(phenyl)silanoxide. Dimethyl(phenyl)silyllithium reacts with 1,2-dibromoethane to give dimethyl(phenyl)silyl bromide, which is so rapidly consumed by excess silyllithium reagent that it does not interfere with the double titration used to measure its concentration. Dimethyl(phenyl)silane, produced by protonation of the silyllithium reagent, is also consumed by the silyllithium reagent to give 1,1,2,2-tetramethyl-1,2-diphenyldisilane, which regenerates the silyllithium reagent, as long as lithium is still present. By-products in the preparation of dimethyl(phenyl)silyllithium include 1,3-diphenyl-1,1,2,2,3,3-hexamethyltrisilane, dimethyldiphenylsilane and 1,4-bis[dimethyl(phenyl)-silyl]benzene. Dimethyl(phenyl)silyllithium displaces the silyl group from the tert-butyldimethylsilyl enol ether of cyclohexanone to give the lithium enolate under relatively mild conditions.
