This biographical article is written like a résumé .(March 2021) |
Kumar Biradha | |
---|---|
Born | 15 June 1968 54) India | (age
Alma mater | D.N.R. College, Andhra University; University of Hyderabad; Saint Mary's University, Canada; Nagoya University. |
Spouse | Satyasri Biradha |
Scientific career | |
Fields | Supramolecular chemistry, Crystal Engineering |
Institutions | Indian Institute of Technology, Kharagpur |
Doctoral advisor | Gautam Radhakrishna Desiraju |
Website | www |
Kumar Biradha is a researcher in the field of crystal engineering. He was born on 15 June 1968 in Relangi, Andhra Pradesh. He is a professor at the Department of Chemistry, Indian Institute of Technology, Kharagpur, [1] and a member of Editorial Advisory board of Crystal Growth & Design , an American Chemical Society Journal. [2] [3]
Biradha completed his secondary and higher secondary education from TMP High School, Relangi, and SVSS Govt. Junior College, Attili, respectively. He obtained his bachelor's degree from DNR College, Bhimavaram, and soon after that he joined University of Hyderabad to complete his M.Sc. in chemistry in 1991. Subsequently, he earned his Ph.D. in structural chemistry from the same university under the guidance of Professor Gautam Radhakrishna Desiraju in 1996. [4] From there he moved to Canada to work as postdoctoral fellow in the laboratory of Mike Zaworotko at Saint Mary's University, Canada in 1997. There he worked on designing various clay-like and zeolite-like architectures by using strong hydrogen bonds and coordination bonds. [5] In the next year he received the prestigious JSPS fellowship to work with Makoto Fujita at IMS, Okazaki, Japan, and Nagoya University, where he expertized on coordination networks and dynamic porous coordination polymers. [6] [7] There he also appointed as an assistant professor and Researcher up to March 2002. Finally he moved back to India and joined the Chemistry Department at IIT Kharagpur as an assistant professor in 2002 and became a professor in 2014. [8]
Biradha's research group aims at synthesizing multi-functional supramolecular materials with the use of distinct crystal engineering strategies. [9] Web of Science has listed over 200 of the published scientific articles by him [10] on Cocrystal, gels, organic polymers, coordination polymers, metal-organic frameworks and covalent organic framework and their potential applications in the fields of electrocatalysis, [11] molecular sensing, solid state [2+2] photo-dimerizations and polymerizations, [12] gas adsorption, inclusion materials, semiconductivity, luminescence, and isomeric hydrocarbon separation. [13] For such significant contributions in science, Biradha featured among 'Top 2% Global scientist' in a study by Stanford Analyst Group [14] under the category of 'Inorganic and Nuclear chemistry'. [15]
A coordination polymer is an inorganic or organometallic polymer structure containing metal cation centers linked by ligands. More formally a coordination polymer is a coordination compound with repeating coordination entities extending in 1, 2, or 3 dimensions.
Crystal engineering studies the design and synthesis of solid-state structures with desired properties through deliberate control of intermolecular interactions. It is an interdisciplinary academic field, bridging solid-state and supramolecular chemistry.
A halogen bond occurs when there is evidence of a net attractive interaction between an electrophilic region associated with a halogen atom in a molecular entity and a nucleophilic region in another, or the same, molecular entity. Like a hydrogen bond, the result is not a formal chemical bond, but rather a strong electrostatic attraction. Mathematically, the interaction can be decomposed in two terms: one describing an electrostatic, orbital-mixing charge-transfer and another describing electron-cloud dispersion. Halogen bonds find application in supramolecular chemistry; drug design and biochemistry; crystal engineering and liquid crystals; and organic catalysis.
Thalappil Pradeep is an institute professor and professor of chemistry in the Department of Chemistry at the Indian Institute of Technology Madras. He is also the Deepak Parekh Chair Professor. In 2020 he received the Padma Shri award for his distinguished work in the field of Science and Technology. He has received the Nikkei Asia Prize (2020), The World Academy of Sciences (TWAS) prize (2018), and the Shanti Swarup Bhatnagar Prize for Science and Technology in 2008 by Council of Scientific and Industrial Research.
4,4′-Bipyridine (abbreviated to 4,4′-bipy or 4,4′-bpy) is an organic compound with the formula (C5H4N)2. It is one of several isomers of bipyridine. It is a colorless solid that is soluble in organic solvents. is mainly used as a precursor to N,N′-dimethyl-4,4′-bipyridinium [(C5H4NCH3)2]2+, known as paraquat.
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Covalent organic frameworks (COFs) are a class of materials that form two- or three-dimensional structures through reactions between organic precursors resulting in strong, covalent bonds to afford porous, stable, and crystalline materials. COFs emerged as a field from the overarching domain of organic materials as researchers optimized both synthetic control and precursor selection. These improvements to coordination chemistry enabled non-porous and amorphous organic materials such as organic polymers to advance into the construction of porous, crystalline materials with rigid structures that granted exceptional material stability in a wide range of solvents and conditions. Through the development of reticular chemistry, precise synthetic control was achieved and resulted in ordered, nano-porous structures with highly preferential structural orientation and properties which could be synergistically enhanced and amplified. With judicious selection of COF secondary building units (SBUs), or precursors, the final structure could be predetermined, and modified with exceptional control enabling fine-tuning of emergent properties. This level of control facilitates the COF material to be designed, synthesized, and utilized in various applications, many times with metrics on scale or surpassing that of the current state-of-the-art approaches.
Rajendra Mishra (1919–1979) was an Indian Professor and education pioneer known for being the one of the founders of the first of the Indian Institutes of Technology (IIT) at IIT Kharagpur, in 1951. He helped establish the institute’s infrastructure, pioneered the engineering disciplines of mechanical, production, and industrial engineering, and launched the study of management science in India. His contributions were unprecedented when he forged a relationship between industry and academia through collaborative programmes. He brought his rich industrial experience to the educational system of IIT Kharagpur and embraced the best engineering and management practices from the US and Europe to build the foundation for a world-class engineering university over a time span of 27 years in India.
Coordination cages are three-dimensional ordered structures in solution that act as hosts in host–guest chemistry. They are self-assembled in solution from organometallic precursors, and often rely solely on noncovalent interactions rather than covalent bonds. Coordinate bonds are useful in such supramolecular self-assembly because of their versatile geometries. However, there is controversy over calling coordinate bonds noncovalent, as they are typically strong bonds and have covalent character. The combination of a coordination cage and a guest is a type of inclusion compound. Coordination complexes can be used as "nano-laboratories" for synthesis, and to isolate interesting intermediates. The inclusion complexes of a guest inside a coordination cage show intriguing chemistry as well; often, the properties of the cage will change depending on the guest. Coordination complexes are molecular moieties, so they are distinct from clathrates and metal-organic frameworks.
A two-dimensional polymer (2DP) is a sheet-like monomolecular macromolecule consisting of laterally connected repeat units with end groups along all edges. This recent definition of 2DP is based on Hermann Staudinger's polymer concept from the 1920s. According to this, covalent long chain molecules ("Makromoleküle") do exist and are composed of a sequence of linearly connected repeat units and end groups at both termini.
Ayyappanpillai Ajayaghosh is a research scientist/academician in the domain of interdisciplinary chemistry, and the former Director of the National Institute for Interdisciplinary Science and Technology. He is known for his studies on supramolecular assemblies, organogels, photoresponsive materials, chemosensory and security materials systems and is an elected fellow of all the three major Indian science academies viz. the National Academy of Sciences, India, Indian National Science Academy and the Indian Academy of Sciences as well as The World Academy of Sciences. The Council of Scientific and Industrial Research, the apex agency of the Government of India for scientific research, awarded him the Shanti Swarup Bhatnagar Prize for Science and Technology, one of the highest Indian science awards for his contributions to Chemical Sciences in 2007. He is the first chemist to receive the Infosys Science Prize for physical sciences, awarded by the Infosys Science Foundation. He received the TWAS Prize of The World Academy of Sciences in 2013 and the Goyal prize in 2019.
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Suman Chakraborty is Professor at the Indian Institute of Technology Kharagpur and Sir J. C. Bose National Fellow ,. He has served as the Dean, Research and Development, Associate Dean and the Head of the School of Medical Science and Technology of the Institute. He has also been Institute/ National Academy of Engineering Chair Professor. He joined the Institute in 2002 as Assistant Professor and has been a Full Professor since 2008.
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Some metal-organic frameworks (MOF) display large structural changes as a response to external stimuli, and such modifications of their structure can, in turn, lead to drastic changes in their physical and chemical properties. Such stimuli-responsive MOFs are generally referred to as a flexible metal-organic frameworks. They can also be called dynamic metal-organic framework, stimuli-responsive MOFs, multi-functional MOFs, or soft porous crystals.
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Topochemical polymerization is a polymerization method performed by monomers aligned in the crystal state. In this process, the monomers are crystallised and polymerised under external stimuli such as heat, light, or pressure. Compared to traditional polymerisation, the movement of monomers was confined by the crystal lattice in topochemical polymerisation, giving rise to polymers with high crystallinity, tacticity, and purity. Topochemical polymerisation can also be used to synthesise unique polymers such as polydiacetylene that are otherwise hard to prepare.
Crystalline sponges are series of organometallic networks developed by Japanese chemist Makoto Fujita. The organic small molecules are absorbed into the void space of the crystalline sponges. Since the organometallic network of crystalline sponges can interact with the small molecule substrates via non-covalent interactions, the absorption can be selective. That is, the crystalline sponge can enrich certain molecules from a mixture.
Sulfidostannates, or thiostannates are chemical compounds containing anions composed of tin linked with sulfur. They can be considered as stannates with sulfur substituting for oxygen. Related compounds include the thiosilicates, and thiogermanates, and by varying the chalcogen: selenostannates, and tellurostannates. Oxothiostannates have oxygen in addition to sulfur. Thiostannates can be classed as chalcogenidometalates, thiometallates, chalcogenidotetrelates, thiotetrelates, and chalcogenidostannates. Tin is almost always in the +4 oxidation state in thiostannates, although a couple of mixed sulfides in the +2 state are known,