プロフィール詳細

プロジェクトを作成

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Dr. Moumita B.に依頼

United States

Inorganic Chemist | Organometallic Chemist | Analytical Chemist | Metal Organic Frameworks | Science Writer

プロフィール概要

Synthetic organometallic and electroanalytical chemist with strong leadership, project management and interpersonal skills- • 6+ years of experience in synthesizing organometallic complexes for solar energy harvesting under photo and electrochemical conditions • 2+ years of applying electroanalytical techniques to optimize the reactivity and selectivity of electrocatalysts • Multiple project management under minimal supervision using effective multi-tasking and time management skills • Recruited and mentored undergraduate researchers and guided them in preparing manuscripts and grant applications • Collaborated with peers in spearheading two distinct research projects, in parallel, in a newly established lab that resulted in a new grant approval and manuscript preparation • Prompt troubleshooting skill in maintaining various chromatography instruments • Excellent communication skill in popularizing science in an exciting and generalized manner for undergraduates (https://chembites.org/author/moukol2011/) and preparing SOPs and grant application TECHNICAL SKILLS NMR IR UV/VIS GC/MS ICP-MS IC PXRD SEM TEM XPS TGA Cyclic Voltammetry Controlled Potential Electrolysis Chemdraw Origin DFT

専門分野

• ★ Inorganic Chemistry
• ★ Renewable Energy
• ☆ Catalysis
• ☆ Materials Science & Engineering
• ☆ Spectroscopy
• ☆ NMR Spectroscopy
• ☆ Electrochemistry
• ☆ Photochemistry
• ☆ Technical & Scientific Writing

サービス

• Writing
• Research
• Consulting
• Data & AI
• Product Development

Writing Clinical Trial Documentation, Technical Writing, Newswriting

Research Market Research, Feasibility Study, Fact Checking, Gray Literature Search, Systematic Literature Review, Secondary Data Collection

Consulting Scientific and Technical Consulting

Data & AI Statistical Analysis, Data Visualization

Product Development Formulation

職務経験

PhD

University of Utah

7月 2014 - 現在

学歴

Master

Jadavpur University

6月 2010 - 7月 2012

認定資格

• 認定資格の詳細は未入力です。

出版物

JOURNAL ARTICLE

(2020). Toward Combined Carbon Capture and Recycling: Addition of an Amine Alters Product Selectivity from CO to Formic Acid in Manganese Catalyzed Reduction of CO2 . Journal of the American Chemical Society. American Chemical Society ({ACS})

(2020). Electrochemical Reduction of Carbamates and Carbamic Acids: Implications for Combined Carbon Capture and Electrochemical CO2 Recycling . Journal of The Electrochemical Society. 167. (8). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 086507. The Electrochemical Society

(2020). The role of leached Zr in the photocatalytic reduction of CO2 to formate by derivatives of UiO-66 metal organic frameworks . Dalton Transactions. 49. (15). Microsoft.AspNetCore.Mvc.Localization.LocalizedHtmlString 4751--4757. Royal Society of Chemistry ({RSC})

(2020). Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst . Chemical Communications. Royal Society of Chemistry ({RSC})

Ni(II) catalyzed bromination of aryl C–H bonds Moumita Bhattacharya, David B. Cluff, Siddhartha Das, Ni(II) catalyzed bromination of aryl C–H bonds, Inorganica Chimica Acta, Volume 423, Part A, 2014, Pages 238-241, ISSN 0020-1693, https://doi.org/10.1016/j.ica.2014.08.012. (http://www.sciencedirect.com/science/article/pii/S0020169314005118) Abstract: Bromination of unactivated aromatic C–H bonds without directing and/or chelating groups was achieved by employing an air stable N-heterocyclic Ni(II) complex. PhI(OAC)2 and N-bromosuccinimide have been used as the oxidizing agent and the bromine source, respectively. Yields for bromination are as high as >99%, especially in presence of electron-withdrawing groups like –NO2 and –CF3. This is a rare report on C–H bond activation with Ni(II) where, instead of homo C–C coupling, reductive elimination to form C-halogen could be achieved. Keywords: Ni(II); C–H activation; Functionalization . Inorganica Chimica Acta.