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(1,8-bis(di-isopropylphosphino)naphthalene)nickel{η2-N2CH(2,6-dimesitylphenyl)} is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1597429-03-2

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1597429-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1597429-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,7,4,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1597429-03:
(9*1)+(8*5)+(7*9)+(6*7)+(5*4)+(4*2)+(3*9)+(2*0)+(1*3)=212
212 % 10 = 2
So 1597429-03-2 is a valid CAS Registry Number.

1597429-03-2Downstream Products

1597429-03-2Relevant academic research and scientific papers

Three-coordinate nickel carbene complexes and their one-electron oxidation products

Iluc, Vlad M.,Hillhouse, Gregory L.

, p. 6479 - 6488 (2014/05/20)

The synthesis and characterization of two new carbene complexes, (dtbpe)Ni-CH(dmp) (1; dtbpe = 1,2-bis(di-tert-butylphosphino)ethane; dmp = 2,6-dimesitylphenyl) and (dippn)Ni-CH(dmp) (2; dippn = 1,8-bis(di-iso- propylphosphino)naphthalene), are described. Complexes 1 and 2 were isolated by photolysis of the corresponding side-bound diazoalkane complexes, exemplified by (dtbpe)Ni{η2-N2CH(dmp)} (3). The carbene complexes feature Ni-C distances that are short and Ni-C-C angles at the carbene carbon that are intermediate between 120° and 180° (155.7(3)° and 152.3(3)°, respectively). The difference between the two carbenes became obvious when their reactivity toward 1-electron oxidizing agents was studied: the oxidation of 1 led to an internal rearrangement and the formation of a nickel(I) alkyl [{κ2-P,C-di-tert-butylphosphino-di-tert-butyl- PCH(dmp)ethane}Ni][BArF4] (4), while the oxidation of 2 allowed the isolation of an unrearranged product, formulated as the cationic nickel(III) carbene complex[(dippn)Ni-CH(dmp)][BArF4] (6). Both oxidations are chemically reversible and the respective reductions lead to the neutral carbene complexes, 1 and 2.

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