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(N,N'-2,6-diisopropylphenyl-β-diketiminate)Nb(NtBu)(η6-C6D6) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1333381-52-4

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1333381-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333381-52-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,3,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1333381-52:
(9*1)+(8*3)+(7*3)+(6*3)+(5*3)+(4*8)+(3*1)+(2*5)+(1*2)=134
134 % 10 = 4
So 1333381-52-4 is a valid CAS Registry Number.

1333381-52-4Relevant academic research and scientific papers

Diniobium inverted sandwich complexes with μ-η6:η6-arene ligands: Synthesis, kinetics of formation, and electronic structure

Gianetti, Thomas L.,Nocton, Grégory,Minasian, Stefan G.,Tomson, Neil C.,Kilcoyne, A. L. David,Kozimor, Stosh A.,Shuh, David K.,Tyliszczak, Tolek,Bergman, Robert G.,Arnold, John

, p. 3224 - 3236 (2013/04/23)

Monometallic niobium arene complexes [Nb(BDI)(NtBu)(R-C6H5)] (2a: R = H and 2b: R = Me, BDI = N,N′-diisopropylbenzene-β-diketiminate) were synthesized and found to undergo slow conversion into the diniobium inverted arene sandwich complexes [[(BDI)Nb(NtBu)]2(μ-RC6H5)] (7a: R = H and 7b: R = Me) in solution. The kinetics of this reaction were followed by 1H NMR spectroscopy and are in agreement with a dissociative mechanism. Compounds 7a-b showed a lack of reactivity toward small molecules, even at elevated temperatures, which is unusual in the chemistry of inverted sandwich complexes. However, protonation of the BDI ligands occurred readily on treatment with [H(OEt2)][B(C6F5)4], resulting in the monoprotonated cationic inverted sandwich complex 8 [[(BDI#)Nb(NtBu)][(BDI)Nb(NtBu)](μ-C6H5)][B(C6F5)4] and the dicationic complex 9 [[(BDI#)Nb(NtBu)]2(μ-RC6H5)][B(C6F5)4]2 (BDI# = (ArNC(Me))2CH2). NMR, UV-vis, and X-ray absorption near-edge structure (XANES) spectroscopies were used to characterize this unique series of diamagnetic molecules as a means of determining how best to describe the Nb-arene interactions. The X-ray crystal structures, UV-vis spectra, arene 1H NMR chemical shifts, and large JCH coupling constants provide evidence for donation of electron density from the Nb d-orbitals into the antibonding π system of the arene ligands. However, Nb L3,2-edge XANES spectra and the lack of sp3 hybridization of the arene carbons indicate that the Nb → arene donation is not accompanied by an increase in Nb formal oxidation state and suggests that 4d2 electronic configurations are appropriate to describe the Nb atoms in all four complexes.

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