Multifunctional phosphine based ligands, 1,1,1-tris(diphenylphosphinomethyl)ethane [CH3C(CH2 PPh2)3][P3] and 1,1,1-tris(diphenylphosphinomethyl)ethane trisulphide [CH3C(CH2P(S)Ph2)3][P3S3] have been introduced to stabilize Au(o)-nanoparticles having small core diameter and narrow size distribution. The Au(o)-nanoparticles were synthesized by the reduction of HAuCl4 precursor with NaBH4 in the presence of ligand P3 or P3S3 using two phases, one pot reaction at room temperature. The Au(o)-nanoparticles exhibit face centered cubic (fcc) lattice having different crystalline shape i.e., single crystallite stabilized by P3 while P3S3 forms decahedral shapes. Surface plasmon bands at -520 nm and TEM study indicate particle size below 2 and 4 nm for Au(o)-nanoparticles stabilized by P3 and P3S3 respectively, which are attributable to the stronger interaction of Au(o) (Soft) with P (Soft) than Au(o) (Soft) with S (less Softer than P). Au(o)-nanoparticles stabilized by P3S3 shows higher thermal stability than that of P3. The synthesized Au(o)-nanoparticles serve as an efficient catalyst for one-pot, three-component (A3) coupling of an aldehyde, an amine and an alkyne via C-H alkyne-activation to synthesize propargylamines (85-96%) without any additives and precaution to exclude air.
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http://dx.doi.org/10.1166/jnn.2013.7576 | DOI Listing |
J Nanosci Nanotechnol
July 2013
Materials Science Division, CSIR-North East Institute of Science and Technology, Jorhat 785 006, Assam, India.
Multifunctional phosphine based ligands, 1,1,1-tris(diphenylphosphinomethyl)ethane [CH3C(CH2 PPh2)3][P3] and 1,1,1-tris(diphenylphosphinomethyl)ethane trisulphide [CH3C(CH2P(S)Ph2)3][P3S3] have been introduced to stabilize Au(o)-nanoparticles having small core diameter and narrow size distribution. The Au(o)-nanoparticles were synthesized by the reduction of HAuCl4 precursor with NaBH4 in the presence of ligand P3 or P3S3 using two phases, one pot reaction at room temperature. The Au(o)-nanoparticles exhibit face centered cubic (fcc) lattice having different crystalline shape i.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
March 2009
Materials Science Division, North-East Institute of Science and Technology, Jorhat 785 006, Assam, India.
The polymeric ruthenium(II) carbonyl complex, [Ru(CO)(2)Cl(2)](n) reacts with 1,1,1-tris-(diphenylphosphinomethyl)ethane trichalcogenide ligands, [CH(3)C(CH(2)P(X)Ph(2))(3)], where X=Se(a), S(b) and O(c) in 1:1 (metal:ligand) molar ratio to afford hexa-coordinated complexes of the type eta(2)-(X,X)-[Ru(CO)(2)Cl(2)P(3)X(3)] (1a-c). The complexes 1a-c exhibit two equally intense nu(CO) bands in the range 1979-2060cm(-1) indicating cis-disposition of the two terminal carbonyl groups. The values of nu(CO) frequencies containing different ligands, in general, follow the order: P(3)O(3)>P(3)S(3)>P(3)Se(3) which may be explained in terms of 'Soft-Hard' (Ru(II)-O) and 'Soft-Soft' (Ru(II)-S/Se) interactions.
View Article and Find Full Text PDFFour acyl-arginyl-p-nitroanilides, nine acetyl-(or benzoyl)-aminoacyl-arginyl-p-nitroanilides and twelve acyl-(or free alpha-amino-)dipeptidyl-arginyl-p-nitroanilides were synthesized, and the kinetic parameters for tryptic hydrolysis of these substrates were determined in 100 mM Tris-HCl buffer, pH 8.0, containing 10 mM CaCl2 at 37 degrees C. Among the acyl-arginyl-p-nitroanilides, Octanoyl-Arg-pNA was hydrolyzed four times more rapidly by trypsin than the commonly used substrate Benzoyl-Arg-pNa.
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