Clarissa O. da Silva

Polarimetry as a Tool for the Study of Solutions of Chiral Solutes

Optical rotation of aqueous solutions of D-levoglucosan was studied experimentally in the 0.03-4.0 mol L(-1) concentration range and a nonlinear concentration dependence of specific optical rotation (SR) was revealed. Discontinuities observed in the concentration plot of SR (at 0.1, 0.3, 0.5, 1.0, and 2.0 mol L(-1)) are well correlated with those found by static and dynamic light scattering and identify concentration ranges in which different solution domains (supramers) may exist. The average SR experimental value for a D-levoglucosan aqueous solution ([α]D(28) -58.5±8.7 deg dm(-1) cm(-3) g(-1)) was found to be in good agreement with values obtained by theoretical calculation (TD-DFT/GIAO) of SR for 15 different conformers revealed by conformational sampling at the PCM/B3LYP/6-311++G(2d,2p)//B3LYP/6-31+G(d,p) level, which were shown to be strongly affected by the solvation microenvironment (0, 1, 2, and 3 explicit solvent molecules considered) due to local geometrical changes induced in the solute molecule. This exceptionally high sensitivity of SR makes polarimetry a unique method capable of sensing changes in the structure of supramers detected in this study.

The (α-1,6) glycosidic bond of isomaltose: a tricky system for theoretical conformational studies

Stable conformations of beta-isomaltose (alpha-D-glucopyranosyl-(1-->6)-beta-D-glucose) in gas-phase and aqueous solution are investigated in this study using quantum mechanical calculations. Conformational maps are calculated at HF/6-31G(d,p) level and lower energy structures are sampled in the most stable regions. Entropic and thermal corrections are considered and the Boltzmann population is obtained for conformers that are representative of the 18 most stable regions found on the potential energy surface. B3LYP/6-31+G(d,p) and B3LYP/6-311+G(2d,2p) calculations are used in conformational samplings. Solvation effects are considered through the polarizable continuum model approach. Hydroxymethyl group orientations are investigated for the most stable conformers. The influence of electronic correlation and solvation on the glycosidic linkage preference (TG, GT, and GG) and hydroxymethyl group orientation (tg, gt, and gg) are discussed. Heteronuclear spin coupling constants ((3)J(C,H)) along the glycosidic linkage are calculated and comparison with other theoretical results and experiments is used to validate the obtained structures.

Specific rotation as a property to validate monosaccharide conformations

Specific rotation ([α](D)) values were calculated for the 15 conformations of xylopyranose that are the most stable in the gas phase and in aqueous solution. The effects of different theoretical descriptions and the medium on the geometry of the conformers and the [α](D) values are evaluated. Differences in [α](D) values found for the same conformer in all descriptions used were smaller than those found between any two different conformers in the same description. The difference between [α](D) values is prominent, even for two conformations that are distinguished from each other only by the orientation of one secondary hydroxyl group. This finding suggests that [α](D) values may potentially be used in the validation of monosaccharide conformations that are theoretically sampled.

Determinação teórica das conformações mais estáveis da trealose em solução aquosa

In this work the most abundant trehalose conformers for the isolated molecule as well as for the water solvated system are selected. The theoretical tecniques employed are ab initio calculations in the gas phase and in aqueous solution using the PCM model. A conformational map is built for the glycosidic angles (F and Y) and the search for the most abundant structures is explained. The final structures are validated by the agreement found between experimental and theoretical values for 3JH,C along the glycosidic linkage.

An Alternative Mechanism for the 1,4-Asymmetric Induction in the Stereoselective Addition of (R)-Pantolactone to 2-Phenylpropylketene

An alternative mechanism for the 1,4-assymmetric induction in the stereoselective addition of (R)-pantolactone to 2-phenylpropylketene was theoretically investigated. A mechanism involving an intermolecular proton transfer assisted by two amine molecules was proposed, which considered the active participation of the dimethylethylamine and its ion as proton transfer agents. In the first step, a neutral dimethylethylamine interacts with the seven-membered ring of the enol intermediate. A specific acid-base interaction is established between the hydroxyl group of the enol and the nitrogen atom of the dimethylethylamine. The neutral dimethylethylamine is basic enough to remove the proton. Another protonated dimethylethylamine is considered to donate its proton to the C=C double bond to give the desired products. The stereochemical outcome was defined by the way that the neutral and protonated dimethylethylamine approached to the enol. The diastereoisomeric ratio found is in good agreement with experiments [for (S, R) and (R, R) it is 99:1].

Conformational study of methylphosphocholine: a prototype for phospholipid headgroups in membranes.

Phospholipid bilayers constitute the largest structural component of cell membranes, in which choline phospholipids are abundant. In this study, through a theoretical sampling on a methylphosphocholine (MePC) potential energy surface, a set of conformers was selected as a prototype for the membrane phospholipid head. We performed a detailed conformational study of such a prototype, both as an isolated moiety and in a solvated system. We used the polarizable continuum model (PCM) to account for solvation effects. We used a quantum-mechanical methodology based on density functional theory (DFT) and the 6-31G(d,p) basis set for the calculations. Through this methodology we were able to obtain a set of conformations that presented a mirror-image pattern, in good agreement with the experimental geometric values for the different phosphocholine derivatives. Potential curves for the main parameters of the dihedral space of MePC were obtained and are provided to guide future force-field parameterizations.

Qual o destino dos programas 3 e 4? A pergunta que não quer calar...

O editorial desta revista, publicado em agosto ultimo, trouxe-me incontrolavel inquietacao. E muito mais por deixar de fora uma questao que considero central neste hemisferio, do que propriamente pelo sinistro futuro que prefigura caso mudancas nao ocorram (previsao de que compartilho). Trata-se de uma pergunta muito simples, e talvez exatamente por isto tenha passado despercebida a tantas cabecas muito mais experientes que a minha. Aqui vai, sem mais delongas: por que nao existem linhas de fomento, na CAPES, destinadas somente [...]