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[Rh2(N,N'-di-p-tolylformamidinate)2(pyrido[2,3-b]pyrazine)2(CF3COO)2] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

526191-29-7

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526191-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 526191-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,6,1,9 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 526191-29:
(8*5)+(7*2)+(6*6)+(5*1)+(4*9)+(3*1)+(2*2)+(1*9)=147
147 % 10 = 7
So 526191-29-7 is a valid CAS Registry Number.

526191-29-7Downstream Products

526191-29-7Relevant academic research and scientific papers

Synthesis and characterization of dirhodium(II,II) formamidinate complexes containing short-bite nitrogen ligands

Tresoldi, Giuseppe,Lo Schiavo, Sandra,Nicolò, Francesco,Cardiano, Paola,Piraino, Pasquale

, p. 190 - 196 (2003)

The Rh24+ complex [Rh2(form)2(O2CCF3)2 (H2O)2] (form=N,N′-di-p-tolylformamidinate anion) easily reacts with the short-bite ligand pyrido[2,3-b]pyrazine, molar ratio 1:2, yielding the complex [Rh2(form)2(pyrido[2,3-b]pyrazine)2 (O2CCF3)2] which has been characterized by conductivity measurements and IR and 1H NMR spectroscopy. The complex exhibits a lantern type structure with the two nitrogen ligands coordinated, in a cisoid arrangement, at the equatorial positions across the dirhodium unit while the axial sites are occupied by two monoligated trifluoroacetate groups. Conductivity and IR data show that in DMSO the complex undergoes dissociation of both the axial ligands leading to the species [Rh2(form)2(pyrido[2,3-b]pyrazine)2(DMSO) 2]2+. The parent compound reacts also with 2-chloro-5,7-dimethyl-1,8-naphtyridine and 2,7-dichloro-5-methyl-1,8-naphtyridine leading to [Rh2(form)2(O2CCF3) (C10H9N2O)(H2O)] and [Rh2(form)2(O2CCF3) (C9H6N2ClO)(H2O)], respectively, in which the dirhodium unit is supported by three different bridging ligands. Microanalysis, 1H NMR and X-ray data unambiguously show that the reaction proceeds, unexpectedly, with elimination of a trifluoroacetate group and the substitution of a chlorine atom of the naphtyridine ligands by oxygen.

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