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Iwao Ojima (born June 5, 1945, in Japan) is a Japanese-American chemist and university distinguished professor at the State University of New York at Stony Brook (Stony Brook University). [1] He has been widely recognized for his seminal contributions to a range of chemical research at the multifaceted interfaces of chemical synthesis and life ...
Karena Chapman is an Australian chemist who is the Joseph W Lauher & Frank W Fowler Endowed Chair in Materials Chemistry at Stony Brook University. Her research considers the use of high energy X-rays to better understand the structure property relationships of energy materials.
Southwest Baptist University (SBU) is a private Baptist university in Bolivar, Missouri. It is affiliated with the Missouri Baptist Convention , which is part of the Southern Baptist Convention . In 2023, it had a total enrollment of 2,168 students enrolled.
Hsiao's laboratory at Stony Brook University aims to understand the structural, morphological development and manipulation of complex polymer systems during preparation and processing in real time at both molecular and nanoscopic scales. [1] [5] [7] [8] [9]
Brookhaven National Laboratory (BNL) is a United States Department of Energy national laboratory located in Upton, New York, a hamlet of the Town of Brookhaven.It was formally established in 1947 at the site of Camp Upton, a former U.S. Army base on Long Island.
The 3D COF called COF-300 [23] and the 2D COF named TpOMe-DAQ [24] are good examples of this chemistry. When 1,3,5-triformylphloroglucinol (TFP) is used as one of the SBUs, two complementary tautomerizations occur (an enol to keto and an imine to enamine) which result in a β-ketoenamine moiety [ 25 ] as depicted in the DAAQ-TFP [ 26 ] framework.
Nancy Sarah Goroff (born February 18, 1968) is an American organic chemist who formerly served as chair of the chemistry department at Stony Brook University. [1] Her research investigates conjugated organic molecules, including polymers, halocarbons and buckyballs.
The formation of the quinoline product is influenced by the interaction of both steric and electronic effects.In a recent study, Sloop [8] investigated how substituents would influence the regioselectivity of the product as well as the rate of reaction during the rate-determining step in a modified Combes pathway, which produced trifluoromethylquinoline as the product.