Gopinadhanpillai Gopakumar

The Cinchona Primary Amine-Catalyzed Asymmetric Epoxidation and Hydroperoxidation of α,β-Unsaturated Carbonyl Compounds with Hydrogen Peroxide

Using cinchona alkaloid-derived primary amines as catalysts and aqueous hydrogen peroxide as the oxidant, we have developed highly enantioselective Weitz-Scheffer-type epoxidation and hydroperoxidation reactions of α,β-unsaturated carbonyl compounds (up to 99.5:0.5 er). In this article, we present our full studies on this family of reactions, employing acyclic enones, 5-15-membered cyclic enones, and α-branched enals as substrates. In addition to an expanded scope, synthetic applications of the products are presented. We also report detailed mechanistic investigations of the catalytic intermediates, structure-activity relationships of the cinchona amine catalyst, and rationalization of the absolute stereoselectivity by NMR spectroscopic studies and DFT calculations.

Polycationic Ligands in Gold Catalysis: Synthesis and Applications of Extremely π-Acidic Catalysts

Very often ligands are anionic or neutral species. Cationic ones are rare, and, when used, the positively charged groups are normally appended to the periphery of the ligand. Here, we describe a dicationic phosphine with no spacer between the phosphorus atom and the two positively charged groups. This structural feature makes its donor ability poorer than that of phosphites and only comparable to extremely toxic or pyrophoric compounds such as PF3 or P(CF3)3. By exploiting these properties, a new Au catalyst has been developed displaying a dramatically enhanced capacity to activate π-systems. This has been used to synthesize very sterically hindered and naturally occurring 4,5-disubstituted phenanthrenes. The present approach is expected to be applicable to the development and improvement of many other transition metal catalyzed transformations that benefit from extremely strong π-acceptor ligands. The mechanism of selected catalytic transformations has been explored by density functional calculations.

Complexation Behavior of the Tri-n-butyl Phosphate Ligand with Pu(IV) and Zr(IV): A Computational Study.

Tri-n-butyl phosphate (TBP), used as the extractant in nuclear fuel reprocessing, shows superior extraction abilities for Pu(IV) over a large number of fission products including Zr(IV). We have applied density functional theory (DFT) calculations to explain this selectivity by investigating differences in electronic structures of Pu(NO3)4·2TBP and Zr(NO3)4·2TBP complexes. On the basis of our quantum chemical calculations, we have established the lowest energy electronic states for both complexes; the quintet is the ground state for the former, whereas the latter exists in the singlet spin state. The calculated structural parameters for the optimized geometry of the plutonium complex are in agreement with the experimental results. Atoms in Molecules analysis revealed a considerable amount of ionic character to M-O{TBP} and M-O{NO3} bonds. Additionally, we have also investigated the extraction behavior of TBP for metal nitrates and have estimated the extraction energies to be -73.1 and -57.6 kcal/mol for Pu(IV) and Zr(IV), respectively. The large extraction energy of Pu(IV) system is in agreement with the observed selectivity in the extraction of Pu.

Bis- and Tris(pyrazolyl)borate/Methane-Stabilized PIII-Centered Cations

We report the synthesis of [H2 B(pz)2 PR](+) , [H2 C(pz)2 PR](+2) , [HB(pz)3 P](+2) , and [HC(pz)3 P](+3) (H2 B(pz)2 =bis(pyrazolyl)borate; H2 C(pz)2 =bis(pyrazolyl)methane; HB(pz)3 =tris(pyrazolyl)borate; HC(pz)3 =tris(pyrazolyl) methane; R=Ph, Cy or Et2 N) by reaction of the corresponding neutral or anionic ligands with chlorophosphines in the presence of TMSOTf. The structures of these compounds were determined by X-ray crystallographic analysis and the nature of their bonding was examined using density functional theory.

Jahn–Teller Distortion in Polyoligomeric Silsesquioxane (POSS) Cations

We investigated the symmetry breaking mechanism in cubic octa-tert-butyl silsesquioxane and octachloro silsesquioxane monocations (Si8O12(C(CH3)3)8(+) and Si8O12Cl8(+)) using density functional theory (DFT) and group theory. Under Oh symmetry, these ions possess (2)T2g and (2)Eg electronic states and undergo different symmetry breaking mechanisms. The ground states of Si8O12(C(CH3)3)8(+) and Si8O12Cl8(+) belong to the C3v and D4h point groups and are characterized by Jahn-Teller stabilization energies of 3959 and 1328 cm(-1), respectively, at the B3LYP/def2-SVP level of theory. The symmetry distortion mechanism in Si8O12Cl8(+) is Jahn-Teller type, whereas in Si8O12(C(CH3)3)8(+) the distortion is a combination of both Jahn-Teller and pseudo-Jahn-Teller effects. The distortion force acting in Si8O12(C(CH3)3)8(+) is mainly localized on one Si-(tert-butyl) group, while in Si8O12Cl8(+) it is distributed over the oxygen atoms. The main distortion forces acting on the Si8O12 core arise from the coupling between the electronic state and the vibrational modes, identified as 9t2g + 1eg + 3a2u for the Si8O12(C(CH3)3)8(+) and 1eg + 2eg for Si8O12Cl8(+).

Investigations of the Boron Buckyball B80: Bonding Analysis and Chemical Reactivity

The boron fullerene B80 is a spherical network of 80 boron atoms, which has a shape similar to the celebrated C60. The 80 Bs span two orbits: while the first contains 60 atoms localised on the vertices of a truncated icosahedron like C60, the second includes 20 extra B atoms capping the hexagons of the frame. Quantum chemical calculations showed that B80 is unusually stable and has interesting physical and chemical properties. Its geometry is slightly distorted from I h to T h symmetry. However, the boron buckyball is only observed in silico, so far the synthesis of this molecule is only a remote possibility. Using DFT at the B3LYP/SVP level, we have analyzed the chemical bonding in B80, the possibility of methyne substitution and the stability of endohedral boron buckyball complexes. A symmetry analysis revealed a perfect match between the occupied molecular orbitals in B80 and C60. The cap atoms transfer their electrons to the truncated icosahedral frame, and they contribute essentially to the formation of σ bonds. The frontier MOs have π character and are localised on the B60 truncated icosahedral frame. The boron cap atoms can be replaced by other chemical groups, such as methyne (CH), which are also able to introduce three electrons in the cage. Symmetrical substitutions of the boron cap atoms by methyne groups in T and T h symmetries revealed two stable endo methyne boron buckyballs, endo-\({\mathrm{B}}_{80-\mathrm{x}}\mathrm{{(CH)}_{x}}\), with x = 4, 8. The stability of these compounds seems to be due to the formation of six boron 4-centre bonding motifs in between the substituted hexagons. These localized bonding motifs are at the basis of the observed symmetry lowering, via a pseudo-Jahn-Teller effect. The methyne hydrogen atoms in the two endohedral fullerenes can be replaced by other atoms, which can lead to cubane or tetrahedral endohedral boron fullerenes. Theoretical study on encapsulated small bases molecules, tetrahedral and cubane like clusters of Group V atoms, showed that the boron buckyball is a hard acid and prefers hard bases like NH3 or N2H4, to form stables off-centred complexes with B80. Tetrahedral and cubane like clusters of this family are usually metastable in the encapsulated state, due to steric strain. The most favorable clusters are mixed tetrahedral and cubane clusters formed by nitrogen and phosphorus atoms such as \(\mathrm{{P}_{2}{N}_{2}@{B}_{80},\ {P}_{3}N@{B}_{80}}\) and P4N4@B80. The boron cap atoms act as electrophilic centres, which react with nucleophilic sites rich in electrons.