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OC5(C6H5)4NiP(C6H5)2CH2CH2P(C6H5)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75901-61-0

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75901-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75901-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,0 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75901-61:
(7*7)+(6*5)+(5*9)+(4*0)+(3*1)+(2*6)+(1*1)=140
140 % 10 = 0
So 75901-61-0 is a valid CAS Registry Number.

75901-61-0Downstream Products

75901-61-0Relevant academic research and scientific papers

ORGANIC CHEMISTRY OF SUBVALENT TRANSITION METAL COMPLEXES XI. OXIDATIVE ADDITIONS OF NICKEL(0) COMPLEXES TO CARBON-CARBON BONDS IN ALKYNES: NICKELIRENES AND NICKELOLES AS CATALYTIC CARRIERS IN THE OLIGOMERIZATION OF ALKYNES

Eisch, John J.,Galle, James E.,Aradi, Allen A.,Boleslawski, Marek P.

, p. 399 - 416 (1986)

The formation of 2,3,4,5-tetraphenylnickelole-bis(triphenylphosphine) (IIIa) and 2,3,4,5-tetraphenylnickelole-bis(1,2-diphenylphosphino)ethane (IIIb), either from (E,E)-1,2,3,4-tetraphenyl-1,3-butadien-1,4-ylidenedilithium (I) and the corresponding nickel(II) chloride-phosphine complexes (II) or from the reduction of η4-tetraphenylcyclobutadienenickel(II) bromide dimer (XII) in the presence of phosphines, proceeds in good yields.Nickelole IIIa displays physical and chemical properties consistent with its structure and is a catalyst for the trimerization of diphenylacetylene.Nickelole IIIb is a highly associated structure but in its chemical response to alkynes, HOAc, O2, Br2, NaAlEt2H2 and heat displays the properties of a nickelole, rather than a cyclobutadienenickel(0) complex.Attempts to generate IIIb photochemically from η4-1,5-cyclooctadiene(η4-tetraphenylcyclopentadienone)nickel and diphos failed, but it was shown that structural types, such as η4-tetraphenylcyclopentadienone(diphos)nickel (a model for the structure suggested by Hoberg and Richter for IIIb), are unstable.Oligomerizations of diphenylacetylene by bis(1,5-cyclooctadiene)nickel were retarded by conducting the reaction in THF or in the presence of diphos.This retardation permitted the interception of products (cis-stilbene and (E,E)-1,2,3,4-tetraphenyl-1,3-butadiene)diagnostic for the intermediacy of nickelirenes and nickeloles.Deuterium labeling verified the presence of carbo-nickel bonds.These trapping experiments, together with findings on the thermal behavior of nickeloles, are combined into a comprehensive view of the cyclotrimerization, cyclotetramerization and linear polymerization of alkynes by nickel(0).

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