Bu-Ali Sina University

About: Bu-Ali Sina University is a education organization based out in Hamadan, Hamadān, Iran. It is known for research contribution in the topics: Catalysis & Adsorption. The organization has 4078 authors who have published 7969 publications receiving 122828 citations.

Cosmological evolution and statefinder diagnostic for new holographic dark energy model in non flat universe

Abstract: In this paper, the holographic dark energy model with new infrared cut-off proposed by Granda and Oliveros has been investigated in spatially non flat universe The dependency of the evolution of equation of state, deceleration parameter and cosmological evolution of Hubble parameter on the parameters of new HDE model are calculated Also, the statefinder parameters r and s in this model are derived and the evolutionary trajectories in s−r plane are plotted We show that the evolutionary trajectories are dependent on the model parameters of new HDE model Eventually, in the light of SNe + BAO + OHD + CMB observational data, we plot the evolutionary trajectories in s−r and q−r planes for best fit values of the parameters of new HDE model

Stereoelectronic power of oxygen in control of chemical reactivity: the anomeric effect is not alone

Abstract: Although carbon is the central element of organic chemistry, oxygen is the central element of stereoelectronic control in organic chemistry. Generally, a molecule with a C–O bond has both a strong donor (a lone pair) and a strong acceptor (e.g., a σ*C–O orbital), a combination that provides opportunities to influence chemical transformations at both ends of the electron demand spectrum. Oxygen is a stereoelectronic chameleon that adapts to the varying situations in radical, cationic, anionic, and metal-mediated transformations. Arguably, the most historically important stereoelectronic effect is the anomeric effect (AE), i.e., the axial preference of acceptor groups at the anomeric position of sugars. Although AE is generally attributed to hyperconjugative interactions of σ-acceptors with a lone pair at oxygen (negative hyperconjugation), recent literature reports suggested alternative explanations. In this context, it is timely to evaluate the fundamental connections between the AE and a broad variety of O-functional groups. Such connections illustrate the general role of hyperconjugation with oxygen lone pairs in reactivity. Lessons from the AE can be used as the conceptual framework for organizing disjointed observations into a logical body of knowledge. In contrast, neglect of hyperconjugation can be deeply misleading as it removes the stereoelectronic cornerstone on which, as we show in this review, the chemistry of organic oxygen functionalities is largely based. As negative hyperconjugation releases the “underutilized” stereoelectronic power of unshared electrons (the lone pairs) for the stabilization of a developing positive charge, the role of orbital interactions increases when the electronic demand is high and molecules distort from their equilibrium geometries. From this perspective, hyperconjugative anomeric interactions play a unique role in guiding reaction design. In this manuscript, we discuss the reactivity of organic O-functionalities, outline variations in the possible hyperconjugative patterns, and showcase the vast implications of AE for the structure and reactivity. On our journey through a variety of O-containing organic functional groups, from textbook to exotic, we will illustrate how this knowledge can predict chemical reactivity and unlock new useful synthetic transformations.