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Azide Ionic Liquids for Safe, Green, and Highly‐Efficient Azidation Reactions to Produce Azide Polymers

Angewandte Chemie, 2023
AbstractAzide compounds are widely used and especially, polymers bearing pendant azide groups are highly desired in numerous fields. However, harsh reaction conditions are always mandatory to achieve full azidation, causing severe side reactions and degradation of the polymers.
Chi Zhang   +8 more
openaire   +2 more sources

The Azide Process

1994
Hydrazine hydrate (1.67 ml = 1.72 g, 34 mmol) is added to a solution of N-benzyloxycarbonyl-S-benzyl-l-cysteinyl-l-seryl-l-histidine methyl ester [1, 2] (5.84 g, 10 mmol) in methanol [3] (50 ml) and the reaction mixture is kept at room temperature for 3 days [4].
Miklos Bodanszky, Agnes Bodanszky
openaire   +2 more sources

The azidation of starch

Carbohydrate Polymers, 2006
Starch is an inexpensive commodity that has been used for non-food purposes for many years. Some of these uses include cross-linked starches that are synthesized with a variety of multifunctional reagents. One unexplored possibility is the use of azides for cross-linking.
Gregory M. Glenn   +7 more
openaire   +2 more sources

Binary Zinc Azides

Chemistry – A European Journal, 2016
AbstractPure, solvent‐free Zn(N3)2 was prepared by reaction of diethyl zinc and hydrazoic acid in aprotic solvents. The single‐crystal structure determination, along with the comprehensive characterization of α‐Zn(N3)2 and two metastable polymorphs, could be achieved for the first time.
Alexander Villinger, Axel Schulz
openaire   +4 more sources

Structure of azide methemoglobin

Journal of Molecular Biology, 1979
Abstract We have compared the structures of horse azide methemoglobin and methemoglobin (MetHb) at 2.8 A resolution by X-ray difference Fourier analysis. Of four low-spin liganded Hb derivatives (nitric oxide Hb, carbon monoxide Hb, cyanide MetHb, and azide MetHb), azide MetHb is closest in structure to MetHb.
James F. Deatherage   +2 more
openaire   +3 more sources

Sensitized photodecomposition of phenyl azide and α-naphthyl azide

J. Chem. Soc., Faraday Trans. 2, 1972
The photodecomposition of phenyl azide and α-naphthyl azide can be induced by triplet sensitizers (aromatic ketones) and by singlet sensitizers (aromatic hydrocarbons). From a comparison of transfer rates with sensitizer energies, and from the spectra and the oxidation potentials of the azides, it appears that two different mechanisms may operate ...
L. J. Leyshon, A. Reiser
openaire   +2 more sources

Synthesis of Glycosyl Azides by the Addition of Phenylselenenyl Azide to Glycals

Journal of Carbohydrate Chemistry, 1994
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Roderick S. Davis   +2 more
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Azide

Mutation Research/Reviews in Genetic Toxicology, 1978
A, Kleinhofs, W M, Owais, R A, Nilan
openaire   +2 more sources

Glycosyl Fluorides and Azides

1962
Publisher Summary This chapter discusses glycosyl fluorides and their derivatives and glycosyl azides and carbohydrates containing fluorine at nonglycosidic carbon atoms. Poly- O -acetylglycosyl halides of the carbohydrates investigate the proportionality relations that exist between the optical rotations and the diameters of the respective halogen ...
Almuth Klemer, Fritz Micheel
openaire   +2 more sources

Mobility of the azide group in aromatic azides

Journal of Applied Spectroscopy, 1976
A. V. Oleinik   +2 more
openaire   +2 more sources

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