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(η(5)-(3-(dimethylamino)propyl)cyclopentadienyl)Ru(dppm)H is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210367-33-2

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210367-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210367-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,3,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 210367-33:
(8*2)+(7*1)+(6*0)+(5*3)+(4*6)+(3*7)+(2*3)+(1*3)=92
92 % 10 = 2
So 210367-33-2 is a valid CAS Registry Number.

210367-33-2Relevant academic research and scientific papers

Intramolecular N-H?H-Ru proton-hydride interaction in ruthenium complexes with (2-(dimethylamino)ethyl)cyclopentadienyl and (3-(dimethylamino)propyl)cyclopentadienyl ligands. Hydrogenation of CO2 to formic acid via the N-H?H-Ru hydrogen-bonded complexes

Chu, Hei Shing,Lau, Chak Po,Wong, Kwok Yin,Wong, Wing Tak

, p. 2768 - 2777 (2008/10/08)

Addition of 1 equiv of HBF4 to (η5-C5H4(CH2) nNMez)RuH(dppm) (n = 2, 3) gave [(η5-C5H4(CH2) nNMe2H+)RuH(dppm)]BF4, in which the amine function was protonated. Relaxation time T1 measurements indicated the existence of an intramolecular N-H?H-Ru hydrogen-bonding interaction in these complexes. A spin saturation transfer study and H/D exchange experiment with [(η-C5H4(CH2)3NMe 2H+)RuH(dppm)]BF4 revealed fast exchange, probably via a dihydrogen complex intermediate, between the hydride ligand and N-H. An attempt to grow single crystals of [(η5-C5H4(CH2) 3NMe2H+)RuH(dppm)]BPh4 for X-ray study resulted in isolation of crystals of the complex, [(η5:η1-C5H4(CH 2)3NMe2)Ru(dppm)]-BPh4, with the chelating (3-(dimethylamino)propyl)cyclopentadienyl ligand. Exposure of [(η5:η1-C5H4(CH 2)3NMe2)Ru(dppm)]-BF4 to 60 atm of H2 at 60 °C gave [(η5-C5H4(CH2) 3-NMe2H+)RuH(dppm)]BF4 within 30 min. Reacting [(η5:η1-C5H4(CH 2)3NMe2)Ru(dppm)]BAr′4 (Ar′ = 3,5-(CF3)2C6H3) with Ph2SiH2 yielded [(η5-C5H4(CH2) 3NMe2H+)RuH(dppm)]BAr′4; it is proposed that hydrolysis of the η2-silane intermediate by adventitious moisture in the solvent affords an η2-dihydrogen species, and heterolytic cleavage of the dihydrogen ligand by the pendant amino group gives the final product. Heating solutions of [(η5:η1-C5H4(CH 2)n-NMe2)Ru(dppm)]BF4 under H2/CO2 (40 atm/40 atm) at 80 °C for 16 h gave formic acid in low yields (n = 2, TON = 6; n = 3, TON = 8). The formation of formic acid is best explained by a mechanism involving intramolecular heterolytic cleavage of the bound H2 to generate [(η5-C5H4(CH2) nNMe2H+)RuH(dppm)]BF4, followed by CO2 insertion into the Ru-H and then N-H protonation of the formato ligand. Carbon disulfide inserted into the Ru-H bond of [(η5-C5H4(CH2) 3NMe2H+)RuH(dppm)]BF4 to give [(η5-C5H4(CH2) 3NMe2H+)Ru(η 1-SCSH)-(dppm)]BF4.

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