New Water‐Soluble N‐Heterocyclic Carbene‐Palladium Complexes as Promising Anti‐Tumor Agents: Investigating DNA and Protein Interactions

2018 ◽  
Vol 3 (21) ◽  
pp. 5709-5716 ◽  
Author(s):  
Prachi S. Bangde ◽  
Dharmendra S. Prajapati ◽  
Prajakta P. Dandekar ◽  
Anant R. Kapdi
2007 ◽  
Vol 111 (46) ◽  
pp. 13325-13335 ◽  
Author(s):  
C. Theiss ◽  
I. Trostmann ◽  
S. Andree ◽  
F. J. Schmitt ◽  
T. Renger ◽  
...  

2019 ◽  
Vol 10 (16) ◽  
pp. 1988-1992 ◽  
Author(s):  
Camille Boucher-Jacobs ◽  
Bo Li ◽  
Charles M. Schroeder ◽  
Damien Guironnet

Water-soluble phosphinosulfonate palladium complexes were synthesized by coordination of a surfactant to the metal center.


2012 ◽  
Vol 2012 ◽  
pp. 1-13 ◽  
Author(s):  
Mala Nath ◽  
Sulaxna ◽  
Xueqing Song ◽  
George Eng

Di- and triorganotin(IV) derivatives of tyrosylalanine (H2Tyr-Ala) with general formula R2Sn(Tyr-Ala) (where R = Me, n-Bu, n-Oct, and Ph) and R3Sn(HTyr-Ala) (where R = Me and Ph) have been synthesized and structurally characterized in the solid state as well as in solution on the basis of various spectroscopic techniques, namely. FT-IR, multinuclear (1H, 13C and 119Sn) NMR and 119Sn Mössbauer. These investigations suggest that tyrosylalanine in R2Sn(Tyr-Ala) acts as dianionic tridentate ligand coordinating through carboxylate oxygen [–C(O)O−], amino (–NH2), and (CO)Npeptide- nitrogen, while in the case of R3Sn(HTyr-Ala), the ligand acts as monoanionic bidentate coordinating through –C(O)O− and –NH2, and the polyhedron around tin in R2Sn(Tyr-Ala) and R3Sn(HTyr-Ala) is a distorted trigonal-bipyramidal. Equilibrium (pH-metric) studies of the interaction of Me2Sn(IV)2+ and Me3Sn(IV)+ with dipeptides namely, tyrosylalanine (H2Tyr-Ala), glycyltyrosine (H2Gly-Tyr), and glycylisoleucine (H2Gly-Ile), in aqueous solution (I = 0.1 M KNO3, 298 K) have also been carried out. The concentration distribution of the various complex species in solution has been evaluated as a function of pH. It has been found that in these dipeptides, [–C(O)O−, N−, NH2] coordinated complexes are dominant in the neutral pH range with a trigonal-bipyramidal structure. The complex species formed are water soluble in the pH range 2.7–10.5. In all of the studied systems, no polymeric species have been detected in the experimental pH range. Beyond pH 8.0, significant amounts of hydroxo species, namely. Me3Sn(OH) and Me2Sn(OH)2, are formed.


Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6652
Author(s):  
Carla Gomes ◽  
Mariana Peixoto ◽  
Marta Pineiro

Metalloporphyrins are involved in many and diverse applications that require the preparation of these compounds in an efficient manner, which nowadays, also involves taking into consideration sustainability issues. In this context, we use ball milling mechanochemistry and sonochemistry for the rational development of synthetic strategies for the sustainable preparation of metalloporphyrins. Zinc, copper, cobalt and palladium complexes of hydrophobic porphyrins were obtained in high yields and under mechanical action with a moderate excess of the metal salt, without any solvent or additive. Sonochemistry prove to be a good alternative for the preparation of metal complexes of water-soluble porphyrins in good yields and short reaction times. Both strategies have good sustainability scores, close to the ideal values, which is useful in comparing and helping to choose the more adequate method.


2014 ◽  
Vol 356 (11-12) ◽  
pp. 2539-2546 ◽  
Author(s):  
Yan Wang ◽  
Xiaolong Yang ◽  
Chunyan Zhang ◽  
Jianqiang Yu ◽  
Jianhua Liu ◽  
...  

1997 ◽  
Vol 62 (2) ◽  
pp. 355-363 ◽  
Author(s):  
Jan Čermák ◽  
Magdalena Kvíčalová ◽  
Vratislav Blechta

New homoleptic nickel(0) and palladium(0) complexes with a water-soluble ligand, 1,3,5-triaza-7-phosphaadamantane, were prepared and characterized by 1H, 13C, and 31P NMR spectra. The complexes, together with the known analogous Ni(0) and Pd(0) complexes with tris(hydroxymethyl)phosphine, were found to be catalysts for buta-1,3-diene oligomerization or telomerization with water in an aqueous biphasic system without a cosolvent or a modifier. Tetrakis[tris(hydroxymethyl)phosphine]nickel (7) preferentially catalyzes oligomerization (both linear and cyclic) in the first example of a nickel-catalyzed buta-1,3-diene oligomerization in an aqueous biphasic system. Palladium complexes give telomers or linear oligomers in quantitative yields. In the case of the triazaphosphaadamantane complex 4, high selectivity to octadienyl ethers (87%) was observed. High values of metal leaching into the product phase in these reactions suggest an easy extraction of starting or intermediate metal complexes caused by the fact that both monomer and products are good ligands for the metal complexes in this particular case.


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