Resume VIVEK SRIVASTAVA, PhD. (Chemistry) Mobile: 07737933821 : E-Mail: viveksrivastava.job@gmail.com CURRENT EMPLOYMENT PROFILE Associated with NIIT University, Neemrana, Rajasthan, as Assistant Professor, Basic Science: Chemistry from 10th July 2012. PREVIOUS EMPLOYMENT (Total Experience: More than 4.5 years) Department of Chemistry, AISECT University, Bhopal. Assistant Professor Chemistry 16th Aug 11 – 2nd July 12 Dept. of Applied Sciences and Humanities, College of Engineering, Teerthankar Mahaveer University, Moradabad. Assistant Professor Chemistry 4th Aug 09 – 6th Aug 10 School of Chemistry and Biochemistry, Thapar University, Patiala. Lecturer-Chemistry 3rd Aug 03– 29th April 06 EDUCATION Post Doc (Chemistry), Laboratory of Molecular Catalysis, Universidade Fedral Do Rio Grande Do Sul, Brazil. Time Period: 10th Aug 2010-12th Aug 2011 (1 Year PostDoc). Ph.D. (Chemistry) from University of Rennes-1, Rennes, France in 2009, PhD titled: Montmorillonite Organic-Inorganic Hybrids derived from Amino acids: Preparation and Use for Heterogeneous Catalysis Time Period: 1st May 2006- 07th July 2009 (3 Year) M.Sc. (Chemistry) from H.N.B. Garahwal University, Srinagar, Uttaranchal in 2003. B.Sc. (Medical) from H.N.B. Garahwal University, Srinagar, Uttaranchal in 2001. AWARDS AND HONOURS a. Felicitated with Ph. D. Fellowship at Indo-French Centre for the Promotion of Advanced Research (IFCPAR), New Delhi and Paris in 2009. b. TWAS- 2009 Postdoctoral Fellowship. c. DST –FAST TRACK Project for 3 years (2013-16) Sponsored Project DST FAST Track: “Ru-immobilized MNPs immobilized on TiO2 will be used for the hydrogenation of carbon dioxide.” Grant Money Rs.2236000: 3 years (started from Dec 2013) PAPER PUBLISHED 1. 2. 3. 4. 5. Vivek Srivastava , "Ionic Liquid Immobilized Palladium Nanoparticle - Graphene Hybrid as Active Catalyst for Heck Reaction " Letters in Organic Chemistry, 12 (2015), 67-72. Praveenkumar Upadhyay, Vivek Srivastava, “Ruthenium nanoparticles intercalated montmorillonite clay for solvent free alkene hydrogenation reaction” RSC Advances 5 740-745, 2014. Vivek Srivastava, “Ru-exchanged MMT Clay with Functionalized Ionic Liquid for Selective Hydrogenation of CO 2 to Formic acid” Catalysis Letters 144, (12) 2221-2226, 2014. Vivek Srivastava, “In Situ Generation of Ru Nanoparticles to Catalyze CO2 Hydrogenation to Formic Acid” Catalysis Letters 144 (10), 1745-1750, 2014. Vivek Srivastava, “Recyclable hydrotalcite clay catalysed Baylis–Hillman reaction” Journal of Chemical Sciences 125 (5), 1207-1212, 2013. 1 Resume 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. Vivek Srivastava, “PEG-Solvent System for L-proline Catalyzed Wieland - Miescher Ketone Synthesis” Current Organocatalysis 1 (1) 2-6, 2014. Vivek Srivastava, “Recyclable L-proline organocatalyst for Wieland–Miescher ketone synthesis”, Journal of Chemical Sciences 125, 1523, 2013. Vivek Srivastava, “An Improved Protocol for Dihydropyrimidines Synthesis” National Academy Science Letters 35 (5), 493-495, 2013. Vivek Srivastava, “An Improved Protocol for Biginelli Reaction” Green and Sustainable Chemistry 3 (2A), 38-40, 2013. Vivek Srivastava, “Ionic-Liquid-Mediated MacMillan’s Catalyst for Diels-Alder Reaction”, Journal of Chemistry, 2013, Article ID 954094, 1-5, 2012. Vivek Srivastava, “An Improved Protocol for the Preparation of New 1, 2, 3 Triazolium Based Ionic Liquids and their Application as solvent for Aldol reaction”, Asymmetric Organocatalysis, 2012, 1, 2. Vivek Srivastava, “Comparison of Supported and Unsupported Proline Derivatives in Asymmetric Aminocatalytic Transformations”, Asymmetric Organocatalysis 1 (1), 8-23, 2012. Vivek Srivastava, “An Improved Protocol for the Aldehyde Olefination Reaction Using (bmim) (NTf 2) as Reaction Medium”, Journal of Chemistry, 2012, 2013, 1. Vivek Srivastava, “Clays: Types and Applications”, Bulletin of the Catalysis Society of India, 2012, 11, 33. (Review article). Vivek Srivastava, “Ionic liquid mediated recyclable Sulphonamide based Organocatalysis for Aldol reaction”, Central European Journal of Chemistry, 2010, 8(2), 269. Vivek Srivastava, Kevin Gaubert, Mathieu Pucheault, Michel Vaultier, “Organic-inorganic hybrid material for enantioselective organocatalysis” ChemCatChem 1(1) 2009 94 – 98. Vasundhara Singh, Varinder Sapehiyia, Vivek Srivastava, “A facile synthesis of biologically active multifunctional Dihydropyrimidinones using ZrO2-pillared clay” Catalysis Communications 2005, 6(1), 57-60. BOOK CHAPTER 1. Alina M. Balu, Antonio Pineda, Juan M. Campelo, Adela I. Carrillo, Noemi Linares, Javier Garcia-Martinez, Elena Serrano, Rafael Luque, Antonio A. Romero, Vivek Srivastava, Supported Pd nanoparticles: synthesis and catalytic applications, Palladium: Compounds, Production and Applications, NovaPublishers, San Diego, USA, 2011 (https://www.novapublishers.com/catalog/product_info.php?products_id=17720) SYMPOSIUM / CONFERENCES 1 “Ruthenium nanoparticles exchanged montmorillonite claycatalyzed Selective alkene hydrogenation” Praveenkumar Upadhyay, Vivek Srivastava, Second International Conference on Nanostructured Materials and Nanocomposites (ICNM 2014)”, 19-21 December 2014 at Mahatma Gandhi University, Kottayam, Kerala, India. 2 “Ionic Liquid Mediated Recyclable Sulphonimide based Organocatalysis for Aldol reaction”, Vivek Srivastava, Neelam Verma, 3rd International IUPAC Conference on Green Chemistry, Canada, 2010. 3 “Recyclable MacMillan Catalyst for Diels Alder Reaction in Ionic Liquid”, Vivek Srivastava, 3rd International IUPAC Conference on Green Chemistry, Canada, 2010. 4 "Improved Protocol for the Aldehyde Olifination Reaction using [bmim][NTf2] as Reaction Medium " Vivek Srivastava, 2nd Asia Pacific Conference on Ionic Liquids and Green Processes Dalian, China, 2010. 5 “Green Protocol for Recyclable Sulphonimide based Organocatalysis for Aldol reaction”, Vivek Srivastava, Neelam Verma, 2nd National Conference on Recent Advances in Chemical & Environmental Sciences (RACES-2010), Patiala, India, 2010. 2 Resume 6 “Ionic Liquid Mediated MacMillan Catalyst for Diels Alder Reaction”, Vivek Srivastava, 2nd National Conference on Recent Advances in Chemical & Environmental Sciences (RACES-2010), Patiala, India, 2010. 7 “Organic-inorganic hybrid materials as heterogeneous catalysts for Asymmetric Aldol Reaction” Vivek Srivastava, Mathieu Pucheault, Vasundhara Singh, Michel Vaultier, 12th National Symposium in Chemistry and 4th CRSI-RSC Symposium in Chemistry, IICT, Hyderabad, 2010. 8 "Design of hybrid task specific onium salt (TSILs)-inorganic matrixes as novel nancomposites for catalysis and synthesis "Vivek Srivastava, Rajni Ratti, Vasundhara Singh, Michel Vaultier, Seminar, Indo-French Center for Organic Synthesis (IFCOS), Dinard, France, 2007. 9 “New Task Specific Ionic Liquid for Conversion of alkyl halide to alkyl azide and for Ugi reaction”, Vivek Srivastava, Sukhbir Kaur, Varinder Sapehiyia, G. L. Kad, Vasundhara Singh, 8 th National Symposium in Chemistry, Indian Institute of Technology, Mumbai, 2006. 10 “Ultrasonically activated oxidation of various mono- and dimethyl-ethers of hydroquinones to quinones catalyzed by CAN-cation exchanged K-10 clay in aqueous media”, Vivek Srivastava, Vasundhara Singh, Varinder Sapehiyia, G. L. Kad, 7th National Symposium in Chemistry, IACS, Kolkata, 2005. 11 “Immobilized functionalised Organic-Clay porous catalysts for Heck and Suzuki reaction”, Vivek Srivastava, Vasundhara Singh, Michel Vaultier, 3rd International Conference of Materials for advanced technologies (ICMRT), Singapore, 2005. Editorial/Review work 1. Ms. Ref. No.: JCOU-D-14-00082 Title: The Kinetics of Carbon Dioxide and Propylene Oxide Copolymerization Catalyzed by Binary Catalyst System: Journal of CO2 Utilization 2. Ms. Ref. No.: JCOU-D-14-00088 Title: DMF and mesoporous Zn/SBA-15 as synergistic catalysts for the cycloaddition of CO2 to propylene oxide : Journal of CO2 Utilization 3. Manuscript: ICBE2886 Title: Study on the Dynamic Change of Index Components during the Growth of Honeysuckle 4. The 3rd International Conference on Biomedical Engineering and Biotechnology(ICBEB 2014) 5. Ms. Ref. No.: BSP-COCAT-2014-24 Title: Enantioselective Desymmetrizations Promoted by Bifunctional Organocatalysts Current Organocatalysis (Bentham Science Publishers) 6. Ms. Ref. No.: BSP-COCAT-2014-24 Submission Title: Enantioselective Desymmetrizations Promoted by Bifunctional Organocatalysts: Current Organocatalysis (Bentham Science Publishers) 7. Journal: Industrial & Engineering Chemistry Research Manuscript ID : ie-2014-00440w Title : "Novel DABCO based ionic liquids: green and efficient catalysts with dual catalytic roles for aqueous Knoevenagel condensation" Editorial Board: 1. Journal of Catalysis, Hindawi Publication Corporation. 2. Indian Journal of Materials Sciences, Hindawi Publication Corporation. 3. Journal of Chemistry, Hindawi Publication Corporation. 4. Working as Technical Program Committee member of 3rd Conference on Catalysis (ICC 2015) will be held from June 12th -14th , 2015 in Suzhou, China. IT SKILLS Conversant with Windows, Office Automation, Mestrec, Chem-Office, Sci-Finder and Internet Application. BEYOND ACADEMIA Secured 1st position in Essay Competition conducted by Nobel Prize Centennial 1901-2001 Commeration (2002), Nanital. Stood 2nd in Working Science Model on National Science Day 2005 conducted by Thapar Institute of Engineering & Technology, Patiala. Certified National Cadet Core (NCC ‘B’). PERSONAL DETAILS Date of Birth : 11th March 1981 Address 3 : C-1/103, Ashiana, Moradabad Resume REFERENCES Name Designation Organization/Institute Mailing Address Telephone Alternate Telephone Fax Email Referee 1 Dr. Karine PHILIPPOT Professor Laboratoire de Chimie de Coordination du CNRS, UPR 8241 205, route de Narbonne, 31077 TOULOUSE cedex 04 Cedex - FRANCE Referee 2 Dr. René GREE Professor Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes 1 Avenue du Général Leclerc 35042 - Rennes Cedex - FRANCE + 33 (0)5 61 33 31 82 Tél.: +33 (0)2 23 23 57 15 | NA NA +33 (0)5 61 55 30 03 Fax.: +33 (0)2 23 23 69 78 karine.philippot@lcc- rene.gree@univtoulouse.fr rennes1.fr 4 Referee 3 (PhD Guide) Dr. Michel Vaultier CNRS Emérite Institut des Sciences Moléculaires Bâtiment A11, Université de Bordeaux 1, 33405 Cedex - FRANCE +33 (0)5 40 00 67 33 NA +33 (0)5 40 00 66 32 michel.vaultier@univrennes1.fr Resume Research Plan My research group is working on the sensible design and development of Catalysts for sustainable processes, which are of primary importance to enable the present and future worldwide production of chemicals while avoiding negative consequences for the environment. State-of-the-art High Pressure Experimentation techniques are employed in the study of the catalytic systems with the aim of promoting scientific research that is fundamental in nature and applied in perspective. We are applying a wide range of synthetic, spectroscopic, and reaction engineering tools to understand the chemical reactions of molecules on catalytic surfaces. Our strong emphasis is placed on the nanoscale fabrication of catalysts by controlling and manipulating the structure of the material. Research projects in my group mainly aimed at addressing current issues associated with alternative energy, renewable chemicals, carbon sequestration and novel catalyst design. Short Term research Plan The design and synthesis of organic-inorganic hybrid composite catalysts is highly desirable in industrial applications. A large number of active homogeneous catalysts, particularly organometallic complexes are currently developed to catalyze several important organic reactions. Nevertheless, supported catalysts are preferable due to operational simplicity; ease of separation and recyclability as well as to limit quantities of waste and by-products generated in the process. While the concept of biphasic catalysis has been around for many years, only few industrial biphasic processes are in operation. This is partly due to the fact that separation of the product from the catalyst phase is rarely perfect, and that catalyst immobilization is seldom completely efficient. Both factors lead to levels of catalyst loss and leaching of active species that cannot be sustained from an economic and/or sustainable perspective. Furthermore, not all catalysts are sufficiently stable for extensive reuses, and the rapid deactivation of many homogeneous catalysts represents a major problem. Considering 2-3 years frame work of my research plan I want to develop multifunctional nanomaterials as catalysts for the synthesis of high added-value chemicals. The major objectives in catalysis are to achive higher efficiencies/selectivities and atom/energy economies, to improve the green credentials of chemical processes. Well-defined metal nanoparticles will be prepared by an organometallic way and immobilized in ionic liquids specially designed. The obtained hybrid TSILs/MNPs will be deposited on inorganic supports for recycling concerns. The catalytic performances of these nanomaterials will be investigated in the synthesis of added-value chemicals including 1) biologically active molecules via multistep processes and 2) fuels/platform molecules via the selective hydrogenation of CO2. Long Term research Plan At a time when the developing world is making huge progress in the production of chemicals, it is imperative that the Indian chemical community strives to stay ahead. This can be achieved by improving the efficiency of chemical processes. My long term research plan aims to provide a platform for the development of new modified chemical processes using the applications of nano-technology along with the unique features of ionic liquids in continuous flow reactor. The major application of this work will be in the high-value-added sector of the chemical industry such as pharmaceutical, fine chemicals, cosmetics, fragrances and flavorings. The combination of flow chemistry with solid-supported catalysts allows the advantages inherent to both technologies to be added together. Thus, the physical immobilization of the catalyst in a packed-bed reactor allows it to be submitted constantly to the reaction conditions, avoiding possible degradation of the catalyst during operations other than the reaction itself (washing, drying, storage, etc.). This frequently leads to a significant extension of the catalyst’s lifetime. In addition, any further processing for the separation of the catalyst from the reaction mixture is no longer needed. The combined effect of these factors is an improvement in the catalyst productivity, with a corresponding reduction in the cost of any given process. The projects under long term research plan will be well focused on the development and the designing of novel nanomaterial via deposition / immobilization / stabilization of various transition metal nanoparticles (e.g. Fe, Co, Pd, Cu, Ru) on task-specific ionic liquids (TSILs) as environmentally compatible supports. Unlike conventionally synthesized nanoparticles, supports offer stabilization (additional stability to nanoparticles) 5 Resume and control (controllable particle size and potentially shapes) as well as the improved material reusability required for tedious organic transformation process and biologically active molecule synthesis. Teaching Statement During my academic career, I’ve had both amazing teachers who have inspired my interest in and respect for their subject and other teachers who have made learning an unbearable chore. Although a cheerful and energetic lecturer is always appreciated, the difference between these two types of teacher may have nothing to do with the friendliness or disposition of the person. I believe what makes a great teacher is the ability to present information in an organized and intuitive sequence, and the art of relating one’s excitement about this information in a way that students can relate it to their own experiences. In chemistry, teachers face the particular challenge of presenting subject material that is often far removed from the tangible experiences of the students. In my career as a teacher I hope to capture my students’ interests by not only sharing my knowledge, but showing them why it is interesting and relevant. For example, the topic of thermodynamics can perhaps seem abstract. However if a student can apply thermodynamics to their experiences, for example understanding why diamonds are said to be “forever”, then the topic becomes tangible, and naturally more interesting. One of my goals as a teacher is to relate my excitement about science to my students by showing them how it is important to their everyday life. The most important step toward bridging experience and abstract scientific principles can also be accomplished through classroom demonstrations and hands-on laboratory sessions. These components are fundamental to learning in science and I believe should be incorporated as much as possible. Learning is accomplished much better through active doing and seeing, than by passively sitting through a lecture. I have learned through my experience with students that showing them chemistry in action is much more valuable and more exciting than telling them about it. I believe that since science is logical and systematic, when it is presented in an organized fashion that is conducive to learning, students are much more capable of grasping the otherwise difficult material. It is my goal as a teacher to be organized and thorough in my lectures so that students have the best chance of grasping the material. I believe the most important thing I can do to help my students learn is to come to every class with enough creative preparation and organization so that I may present an engaging, coherent and intuitive lecture. This foundation will allow me to translate my excitement and interest in the subjects that I teach in order to promote student learning and interest in the sciences. I hereby declare that I have carefully read and understood the instructions, and that the entries in this form as well as in attached sheets are true to the best of my knowledge and belief. Date: Jan 13th 2015 Place: Neemrana (Signature of Applicant) 6