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[(η5-C5Me5)Ru(dppe)(CCC[=C(CN)2]CH=C(CN)2)] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1346414-83-2

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1346414-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346414-83-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,4,1 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1346414-83:
(9*1)+(8*3)+(7*4)+(6*6)+(5*4)+(4*1)+(3*4)+(2*8)+(1*3)=152
152 % 10 = 2
So 1346414-83-2 is a valid CAS Registry Number.

1346414-83-2Downstream Products

1346414-83-2Relevant academic research and scientific papers

Substitution of tetracyanoethene by ethynyl-metal complexes gives tricyanovinylethynyl (tricyanobutenynyl) derivatives: Syntheses, protonation, and addition of metal-ligand fragments

Bruce, Michael I.,Fox, Mark A.,Low, Paul J.,Nicholson, Brian K.,Parker, Christian R.,Patalinghug, Wyona C.,Skelton, Brian W.,White, Allan H.

, p. 2639 - 2657 (2012/06/04)

A series of complexes containing the new tricyanovinylethynyl (3,4,4-tricyanobut-3-en-1-ynyl) ligand have been obtained by substitution of a CN group in tetracyanoethene upon reaction with the ethynyl complexes M(C≡CH)(PP)Cp′ (M = Ru, Os, (PP)Cp′ = (PPh3) 2Cp; M = Ru, PP = dppe, Cp′ = Cp, Cp*). The reactions proceed in higher yield as the metal environment becomes more sterically hindered, the normal [2 + 2]-cycloaddition/ring-opened product M{C[=C(CN) 2]CH=C(CN)2}(PP)Cp′ also being formed in some cases. The diynyl complex Ru(C≡CC≡CH)(dppe)Cp* reacts with tcne to give only the ring-opened adduct Ru{C≡CC[=C(CN)2]CH=C(CN) 2}(dppe)Cp*. Protonation (HBF4 or HPF6) of Ru{C≡CC(CN)=C(CN)2}(dppe)Cp* afforded the vinylidene cation [Ru{=C=CHC(CN)=C(CN)2}(dppe)Cp*]+. A second transition-metal fragment MLn (MLn = Ru(PPh 3)2Cp, M′(dppe)Cp* (M′ = Ru, Os), RuCl(dppe)2) can be added to the CN group trans to the metal center; electrochemical, spectroscopic, and computational studies indicate that there is little ground-state delocalization between the metal centers. In the case of the tricyanovinylethynyl derivatives, an intense MLCT (or ML-LCT) transition can be identified in the visible region, which is responsible for the intense blue to purple color of these species; the analogous transition in the vinylidene-based complexes is significantly blue-shifted. The X-ray crystallographically determined structures of several of these complexes are reported. The cations [{Cp*(dppe)Ru}{μ-(C/N)≡CC(CN)=C(CN) (≡C/N)}{M(dppe)Cp*}]+ (M = Ru, Os) show some C≡C/C≡N disorder (and associated Ru/Os disorder in the case of the heterometallic example) in the crystals.

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