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[bis(N-(2,6-diisopropylphenyl)iminobenzyl-κN,N')pyridine-κN]CoCl2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

301658-96-8

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301658-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 301658-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,6,5 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 301658-96:
(8*3)+(7*0)+(6*1)+(5*6)+(4*5)+(3*8)+(2*9)+(1*6)=128
128 % 10 = 8
So 301658-96-8 is a valid CAS Registry Number.

301658-96-8Relevant academic research and scientific papers

Chelate bis(imino)pyridine cobalt complexes: Synthesis, reduction, and evidence for the generation of ethene polymerization catalysts by Li+ cation activation

Kleigrewe, Nina,Steffen, Winfried,Bloemker, Tobias,Kehr, Gerald,Froehlich, Roland,Wibbeling, Birgit,Erker, Gerhard,Wasilke, Julia-Christina,Wu, Guang,Bazan, Guillermo C.

, p. 13955 - 13968 (2007/10/03)

Treatment of the bis(iminobenzyl)pyridine chelate Schiff-base ligand 8 (ligPh) with FeCl2 or CoCl2 yielded the corresponding (ligPh)MCl2 complexes 9 (Fe) and 10 (Co). The reaction of 10 with methyllithium or "butadiene-magnesium" resulted in reduction to give the corresponding (ligPh)Co(I)Cl product 11. Similarly, the bis(aryliminoethyl)pyridine ligand (ligMe) was reacted with CoCl2 to yield (ligMe)CoCl2 (12). Reduction to (ligMe)CoCl (13) was effected by treatment with "butadiene-magnesium". Complex 13 reacted with Li[B(C 6F5)4] in toluene followed by treatment with pyridine to yield [(ligMe)Co+-pyridine] (15). The reaction of the Co(II) complexes 10 or 12 with ca. 3 molar equiv of methyllithium gave the cobalt(I) complexes 16 and 17, respectively. Treatment of the (lig Me)CoCH3 (17) with Li[B(C6F5) 4] gave a low activity ethene polymerization catalyst. Likewise, complex 16 produced polyethylene (activity = 33 g(PE) mmol(cat)-1 h-1 bar-1 at room temperature) upon treatment with a stoichiometric amount of Li[B(C6F5)4]. A third ligand (ligOMe) was synthesized featuring methoxy groups in the ligand backbone (22). Coordination to FeCl2 and CoCl2 yielded the desired compounds 23 and 24. Reaction with MeLi gave (lig OMe)CoMe (25/26). Treatment of 25/26 with excess B(C 6F5)3 gave the η6-arene cation complex 27, where one Co-N linkage was cleaved. Activation of 25/26 with Li[B(C6F5)4] again gave a catalytically active species.

Generation of bis(iminoalkyl)pyridine cobalt(I) cations under metal alkyl free conditions that polymerize ethene

Steffen, Winfried,Bloemker, Tobias,Kleigrewe, Nina,Kehr, Gerald,Froehlich, Roland,Erker, Gerhard

, p. 1188 - 1189 (2007/10/03)

Treatment of the bis(iminoethyl)- or bis(iminobenzyl)pyridine cobalt dichlorides 3a,b with "butadiene-magnesium" (a, R = CH3) or methyllithium (b, R = Ph) yields the corresponding bis(iminoalkyl)pyridine cobalt(i) chloride complexes 7a,b. Chlor

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