Biomedical subjects

M Elango

Publications and source records attributed to M Elango.

12 recordsLinked to original sources

PubMed2006

pKa prediction using group philicity.

Acid-base dissociation constants (pK(a) values) are important in understanding the chemical, environmental and toxicological properties of molecules. Though various methods have been developed to predict pK(a) by experimental and theoretical models, prediction of pK(a) is still complicated. Hence, a new approach for predicting pK(a) using the group philicity concept has been attempted. Presence of known functional groups in a molecule is utilized as the most important indicator to predict pK(a). The power of this descriptor in describing pK(a) for the series of carboxylic acids, various substituted phenols, anilines, phosphoric acids, and alcohols is probed. Results reveal that the group electrophilicity is suitable for effectively predicting the pK(a) values.

Journal Article↗

PubMed2006

Hydrogen peroxide clusters: the role of open book motif in cage and helical structures.

Hartree-Fock (HF) calculations using 6-31G*, 6-311++G(d,p), aug-cc-pVDZ, and aug-cc-pVTZ basis sets show that hydrogen peroxide molecular clusters tend to form hydrogen-bonded cyclic and cage structures along the lines expected of a molecule which can act as a proton donor as well as an acceptor. These results are reiterated by density functional theoretic (DFT) calculations with B3LYP parametrization and also by second-order Møller-Plesset perturbation (MP2) theory using 6-31G* and 6-311++G(d,p) basis sets. Trends in stabilization energies and geometrical parameters obtained at the HF level using 6-311++G(d,p), aug-cc-pVDZ, and aug-cc-pVTZ basis sets are similar to those obtained from HF/6-31G* calculation. In addition, the HF calculations suggest the formation of stable helical structures for larger clusters, provided the neighbors form an open book structure.

Algorithms↗

PubMed2005

Density functional theoretical investigation on influence of heterosubstitution and benzannelation on the thermal 6pi electrocyclization of cis-cyclononatetraene.

Thermal 6pi electrocyclization of cyclononatetraene (CNT), its hetero-substituted analogues, and its benzannelated derivatives have been investigated by using the B3LYP method employing 6-31G* and 6-311+G** basis sets. The results indicate that heterosubstitution and benzannelation influence the rate of cyclization. Nucleus independent chemical shifts (NICS), conceptual density functional theory (DFT) based reactivity descriptors, group electronegativity values, and barriers to planarity provide complementary evidence for the predicted rate of cyclization. The available experimental data are in good agreement with the computed values.

Journal Article↗

PubMed2005

Stability and reactivity of all-metal aromatic and antiaromatic systems in light of the principles of maximum hardness and minimum polarizability.

It is demonstrated that among various possible isomers of all-metal aromatic compounds such as Al(4)(2-) and their complexes the most stable isomer with the minimum energy is the hardest and the least polarizable. A similar situation is observed for different isomers of all-metal antiaromatic compounds such as Al(4)(4-) and their complexes. It is shown that linear Al(4)(4-) is energetically more stable than its cyclic isomer. The reaction energies associated with the complexation processes highlight the stability of those complexes. The difference in energy, hardness, and polarizability between a cyclic molecule and its linear counterpart convincingly shows that an aromatic molecule exhibits negative changes in energy and polarizability but positive changes in hardness as expected from the principles of minimum energy, minimum polarizability, and maximum hardness. Although the aromaticity of Al(4)(2-) is unequivocally established through this study, the antiaromaticity picture in the case of Al(4)(4-) is shown to be poorly understood;however, the present analysis sheds light on this controversy.

Journal Article↗

PubMed2005

Bowls, balls and sheets of boric acid clusters: the role of pentagon and hexagon motifs.

Ab initio calculations suggest the possibility of forming boric acid clusters in the laboratory. The most stable form of the boric acid dimer contains two hydrogen bonds, similar to the carboxylic acid dimers. Though the trimer and the tetramer form extensions of this geometry, the pentamer prefers a bowl shape. Any addition of boric acid molecules to this geometry leads to bowl-shaped structures with the 15-mer forming a (3/4)buckyball and the 20-mer a full-fledged buckyball. The hexamer, on the other hand, prefers to stay planar as a hexagon-centered rosette. Any further extension of this geometry leads to planar structures as long as a pentagon is not included.

Boric Acids↗

PubMed1996