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[(N(C6H2{C(H)Ph2}2Me-2,6,4)(SiMe3))GeCl] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1338823-95-2

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1338823-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338823-95-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,8,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1338823-95:
(9*1)+(8*3)+(7*3)+(6*8)+(5*8)+(4*2)+(3*3)+(2*9)+(1*5)=182
182 % 10 = 2
So 1338823-95-2 is a valid CAS Registry Number.

1338823-95-2Upstream product

1338823-95-2Relevant academic research and scientific papers

Extremely bulky amido-group 14 element chloride complexes: Potential synthons for low oxidation state main group chemistry

Li, Jiaye,Stasch, Andreas,Schenk, Christian,Jones, Cameron

, p. 10448 - 10456 (2011/12/13)

The preparation of a series of extremely bulky secondary amines, Ar*N(H)SiR3 (Ar* = C6H2{C(H)Ph 2}2Me-2,6,4; R3 = Me3, MePh 2 or Ph3) is described. Their deprotonation with either LiBun, NaH or KH yields alkali metal amide complexes, several monomeric examples of which, [Li(L){N(SiMe3)(Ar*)}] (L = OEt2 or THF), [Na(THF)3{N(SiMe3)(Ar*)}] and [K(OEt2){N(SiPh3)(Ar*)], have been crystallographically characterised. Reactions of the lithium amides with germanium, tin or lead dichloride have yielded the first structurally characterised two-coordinate, monomeric amido germanium(ii) and tin(ii) chloride complexes, [{(SiR3)(Ar*)N}ECl] (E = Ge or Sn; R = Me or Ph), and a chloride bridged amido-lead(ii) dimer, [{[(SiMe3)(Ar*)N] Pb(μ-Cl)}2]. DFT calculations on [{(SiMe3)(Ar*)N} GeCl] show its HOMO to exhibit Ge lone pair character and its LUMO to encompass its Ge based p-orbital. A series of bulky amido silicon(iv) chloride complexes have also been prepared and several examples, [{(SiR3)(Ar*)N} SiCl3] (R3 = Me3, MePh2) and [{(SiMe3)(Ar*)N}SiHCl2], were crystallographically characterised. The sterically hindered group 14 complexes reported in this study hold significant potential as precursors for kinetically stabilised low oxidation state and/or low coordination number group 14 complexes.

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