Density functional study on the effect of a new ladder-type structure with different substituent groups (R = H, CH3, OCH3and CN) for donor–acceptor copolymers

RSC Advances ◽  
2014 ◽  
Vol 4 (69) ◽  
pp. 36656 ◽  
Author(s):  
Zhiyong Fu ◽  
Wei Shen ◽  
Rongxing He ◽  
Xiaorui Liu ◽  
Pei Yu ◽  
...  
Keyword(s):  
Density Functional ◽  
Type Structure ◽  
Functional Study ◽  
Density Functional Study ◽  
Donor Acceptor

A Gas- and Condensed-Phase Density Functional Study of Donor−Acceptor Complexes of Sulfur Trioxide

2006 ◽  
Vol 110 (17) ◽  
pp. 5831-5838 ◽  
Author(s):  
Brian N. Ida ◽  
Peter S. Fudacz ◽  
Douglas H. Pulsifer ◽  
Jean M. Standard
Keyword(s):  
Condensed Phase ◽  
Sulfur Trioxide ◽  
Density Functional ◽  
Functional Study ◽  
Density Functional Study ◽  
Phase Density ◽  
Donor Acceptor

Density functional study on the effect of substituent group for the monomer of donor-acceptor copolymer

2010 ◽  
Vol 48 (20) ◽  
pp. 2099-2107 ◽  
Author(s):  
Lei Sun ◽  
Fu-Quan Bai ◽  
Zeng-Xia Zhao ◽  
Bao-Zhu Yang ◽  
Hong-Xing Zhang
Keyword(s):  
Density Functional ◽  
Functional Study ◽  
Density Functional Study ◽  
Substituent Group ◽  
Donor Acceptor

Molecular Structure and Bonding in Platinum-Picoline Anticancer Complex: Density Functional Study

2004 ◽  
Vol 69 (1) ◽  
pp. 63-72 ◽  
Author(s):  
Danuta Michalska ◽  
Rafał Wysokiński
Keyword(s):  
Molecular Structure ◽  
Steric Hindrance ◽  
Density Functional ◽  
Anticancer Agent ◽  
Basis Set ◽  
Functional Study ◽  
Molecular Plane ◽  
Density Functional Study ◽  
Donor Acceptor ◽  
Insight Into

Density functional study has been performed for a new anticancer agent, cis-[PtCl2(NH3)(2-picoline)] (1), AMD473, now clinically tested. The molecular structure, natural charges, orbital occupancies, vibrational frequencies and metal-ligand stretching force constants were calculated using the modified Perdew-Wang functional (mPW1PW) with the combined D95V(d,p) and LANL2DZ basis set. For comparison, analogous calculations were performed for: cis-[PtCl2(NH3)(3-picoline)] (2), cis-[PtCl2(NH3)(pyridine)] (3) and cisplatin. The interesting structural feature of 1 is almost perpendicular orientation of the 2-picoline ligand with respect to the molecular plane. In the remaining complexes, 2 and 3, the tilt of the pyridine ring is smaller. The position of the methyl group in 1 introduces steric hindrance to an axial approach of the Pt metal. The natural bond analysis (NBO) has provided detailed insight into the electronic donor-acceptor interactions within the platinum coordination sphere. The results clearly indicate that the Pt-N(py) bond is stronger than Pt-NH3 bond, and the Pt-Cl bond trans to 2-picoline is weaker than the cis Pt-Cl bond. Thus, both the trans effect of the 2-picoline ligand and a steric hindrance of Pt in 1 can be of key importance in the different mode of binding of this drug to DNA, in comparison with cisplatin.

Sign in / Sign up

Export Citation Format

Share Document