Results 291 to 300 of about 5,249,633 (346)

Polymerase Synthesis of Hypermodified DNA Displaying a Combination of Thiol, Hydroxyl, Carboxylate, and Imidazole Functional Groups in the Major Groove. [PDF]

Chemistry
Kaiser L, Ondruš M, Poštová Slavětínská L, Raindlová V, Hocek M.   +4 more
europepmc   +1 more source

Phenolic Composition, Functional Groups, In Vitro Bioactivities, and Techno-Functional Properties of Whole and Composite Bioprocessed Flours From Cowpea, Sorghum and Orange-Fleshed Sweet Potato. [PDF]

J Food Sci
Kewuyemi YO, Chinma CE, Kesa H, Adebo OA.   +3 more
europepmc   +1 more source

Regulating the Structure and Optical Properties of Graphitic Carbon Nitride by Tuning Edge Aromatic Functional Groups. [PDF]

ACS Omega
He J, Guo H, Guo Y, Lan Y, Li X, Li Y, Ju H.   +6 more
europepmc   +1 more source

Machine-Learning Approach to Identify Organic Functional Groups from FT-IR and NMR Spectral Data. [PDF]

ACS Omega
Lee G, Shim H, Cho J, Choi SI.
europepmc   +1 more source

Surveying Phase Modifier Functional Groups for Applications to Ln(III) Separations. [PDF]

ACS Omega
Peroutka AA, Servis MJ, Shafer JC.
europepmc   +1 more source

Modulating the oxygen affinity of porphyrins with metals, ligands, and functional groups: A DFT study. [PDF]

J Comput Chem
Ovalle S, Malardier-Jugroot C.
europepmc   +1 more source

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Functional group analysis

Analytical Chemistry, 1972
Analytical methods for functional group analysis are reviewed. Literature reviewed is from the period of December 1983 through November 1985 and presents methods for determining the following compounds: acids, acid halides, active hydrogen, alcohols, aldehydes, ketones, amides, amines, amino acids, anhydrides, aromatic hydrocarbons, azo compounds ...
W T, Smith, J M, Patterson
openaire   +3 more sources

Functional Group Basis Sets

Journal of Chemical Theory and Computation, 2005
The electronic properties of molecular functional groups (methyl, benzyl, etc.) are generally conserved across different molecules. However, atomic basis sets use the same electronic variational space on an element regardless of the functional group it is in.
Benjamin G, Janesko, David, Yaron
openaire   +2 more sources

A Photobasic Functional Group

Journal of the American Chemical Society, 2015
Controlling chemical reactivity using light is a longstanding practice within organic chemistry, yet little has been done to modulate the basicity of compounds. Reported herein is a triazabutadiene that is rendered basic upon photoisomerization. The pH of an aqueous solution containing the water-soluble triazabutadiene can be adjusted with 350 nm light.
Jie, He, Flora W, Kimani, John C, Jewett
openaire   +2 more sources