Debashis Chakraborty

Bio: Debashis Chakraborty is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Polymerization & Ring-opening polymerization. The author has an hindex of 30, co-authored 112 publications receiving 2178 citations. Previous affiliations of Debashis Chakraborty include Colorado State University & University of Göttingen.

Salen Complexes of Zirconium and Hafnium: Synthesis, Structural Characterization, Controlled Hydrolysis, and Solvent-Free Ring-Opening Polymerization of Cyclic Esters and Lactides

Abstract: Dinuclear salen compounds of zirconium and hafnium are efficient initiators for the solvent-free ring-opening polymerization of cyclic ester monomers and lactides. There is a correlation between the theoretical and experimental number-average molecular weights (Mn's) in these polymerizations. Polymerization of β-butyrolactone gives poly(3-hydroxybutyrate) with a good Mn and molecular weight distribution.

Decolorization and degradation of methyl orange by Bacillus stratosphericus SCA1007

Abstract: The present study deals with complete decolorization and degradation of sulfonated azo dye (Methyl orange) by Bacillus stratosphericus SCA1007. These classes of dyes are difficult to degrade by conventional treatment methods. To overcome this problem, an environment friendly and efficient method was developed to degrade this recalcitrant dye. Bacillus stratosphericus SCA1007 could carry out complete decolorization of Methyl orange in a wide range up to 150 mg/L of dye concentration, at temperature 35 °C and pH 7 under static condition along with yeast extract in minimal salt media. This is the first study demonstrating complete decolorization of Methyl orange by Bacillus stratosphericus SCA1007 under optimized conditions within 12 h of incubation. The degradation of dye was studied by UV-vis and FTIR. Toxicity studies were performed on Escherichia coli and Vigna radiata to confirm the non-toxic nature of the degraded products.

Controlled ring-opening polymerization of lactide and glycolide.

Abstract: 23 Stereocontrol of Lactide ROP 6164 231 Isotactic Polylactides 6164 232 Syndiotactic Polylactides 6166 233 Heterotactic Polylactides 6166 3 Anionic Polymerization 6166 4 Nucleophilic Polymerization 6168 41 Mechanistic Considerations 6168 42 Catalysts 6169 421 Enzymes 6169 422 Organocatalysts 6169 43 Stereocontrol of Lactide ROP 6170 44 Depolymerization 6170 5 Cationic Polymerization 6170 6 Conclusion and Perspectives 6171 7 Acknowledgments 6173 8 References and Notes 6173

π-Bonding and the Lone Pair Effect in Multiple Bonds Involving Heavier Main Group Elements: Developments in the New Millennium

Abstract: This review is essentially an update of one entitled “πBonding and The Lone Pair Effect in Multiple Bonds Between Heavier Main Group Elements” which was published more than 10 years ago in this journal.1 The coverage of that survey was focused on the synthesis, structure, and bonding of stable compounds2 of heavier main group elements that correspond to the skeletal drawings reproduced in Tables 1 and 2. A row of numbers is listed at the bottom of each column in these tables. This refers to the number of stable complexes from each class that are currently known. The numbers in parentheses refer to the number of stable species that were known at the time of the previous review. Clearly, many of the compound classes listed have undergone considerable expansion although some remain stubbornly rare. The most significant developments for each class will be discussed in detail under the respective sections. As will be seen, there are also a limited number of multiple bonded heavier main group species that do not fit neatly in the classifications in Tables 1 and 2. However, to keep the review to a manageable length, the limits and exclusions, which parallel those used earlier, are summarized as follows: (i) discussion is mainly confined to compounds where experimental data on stable, isolated species have been obtained, (ii) stable compounds having multiple bonding between heavier main group elements and transition metals are not generally discussed, (iii) compounds in which a multiple bonded heavier main group element is incorporated within a ring are generally not covered, and (iv) hypervalent main group compounds that may incorporate faux multiple bonding are generally excluded. Such compounds are distinguished from those in Tables 1 and 2 in that they apparently require the use of more than four valence bonding orbitals at one or more of the bonded atoms. The remainder of this review is organized in a similar manner to that of the previous one wherein the compounds to be discussed are classified according to those summarized in Tables 1 and 2. The key unifying feature of almost all molecules discussed in this review is that they are generally stabilized by the use of bulky substituents which block associative or various decomposition pathways.3 Since the previous review was published in 1999, several review articles that cover parts of the subject matter have appeared.4