THE CHARACTERIZATION OF TRI-O-TOSYL SUCROSE

1959 ◽  
Vol 37 (3) ◽  
pp. 575-578 ◽  
Author(s):  
P. D. Bragg ◽  
J. K. N. Jones
Keyword(s):  
Hydroxyl Groups ◽  
Primary Hydroxyl

Tri-O-tosyl sucrose was synthesized by the action of p-tolylsulphonyl chloride upon sucrose in pyridine, and the tosyl groups were shown by methylation to be mainly (84%) located on the three primary hydroxyl groups.

Synthesis and characterization of α-butyl-ω-{3-[(2,2- dihydroxymethyl)-propionyloxy]}propyl polydimethyl siloxane

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Meng Zhang ◽  
Yuanjuan Wu ◽  
Qingsi Zhang ◽  
Tianduo Li
Keyword(s):  
Ring Opening ◽  
Ring Opening Polymerization ◽  
Synthesis And Characterization ◽  
Hydroxyl Groups ◽  
Single Chain ◽  
Polydimethyl Siloxane ◽  
Primary Hydroxyl ◽  
Anionic Ring

AbstractA novel polydimethylsiloxane containing two primary hydroxyl groups at one single chain end was synthesized by five-step reactions which included esterification, hydroxyl protection, anionic ring-opening polymerization, hydrosilylation and deprotection. The prepared compounds in each step were characterized. The results showed that at each step synthesis was successfully carried out and objective products could be achieved.

The Preparation and Characterization of Starch Oxidized by Nitric Acid and its Properties of Calcium Complexing Capacity

2013 ◽  
Vol 652-654 ◽  
pp. 1593-1596 ◽  
Author(s):  
Xue Chuan Wang ◽  
Fei Hu Li ◽  
Tao Tao Qiang
Keyword(s):  
Nitric Acid ◽  
Carboxylic Acids ◽  
Hydroxyl Groups ◽  
Oxidized Starch ◽  
Complexing Capacity ◽  
Primary Hydroxyl ◽  
Ft Ir

The primary hydroxyl groups of Starch Oxidized by nitric acid to the corresponding carboxylic acids has been investigated. The structure of the Oxidized-Starch(OS) was characterized by FT-IR, 1HNMR and GPC. The predicated product was obtained from the results. Its application in calcium complexing capacity has been discussed. The calcium complexing capacity of OS may up to 119.39 mg/g. The data confirmed that the starch oxidized by nitric acid had excellent capacity of calcium complexing.

scholarly journals Synthesis, Fabrication, and Characterization of Functionalized Polydiacetylene Containing Cellulose Nanofibrous Composites for Colorimetric Sensing of Organophosphate Compounds

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1869
Author(s):  
A K M Mashud Alam ◽  
Donovan Jenks ◽  
George A. Kraus ◽  
Chunhui Xiang
Keyword(s):  
Solid State ◽  
Hydroxyl Groups ◽  
Colorimetric Sensing ◽  
Electrospinning Technique ◽  
Hazardous Chemical ◽  
Tensile Tester ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Landmark Study

Organophosphate (OP) compounds, a family of highly hazardous chemical compounds included in nerve agents and pesticides, have been linked to more than 250,000 annual deaths connected to various chronic diseases. However, a solid-state sensing system that is able to be integrated into a clothing system is rare in the literature. This study aims to develop a nanofiber-based solid-state polymeric material as a soft sensor to detect OP compounds present in the environment. Esters of polydiacetylene were synthesized and incorporated into a cellulose acetate nanocomposite fibrous assembly developed with an electrospinning technique, which was then hydrolyzed to generate more hydroxyl groups for OP binding. Scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), Instron® tensile tester, contact angle analyzer, and UV–Vis spectroscopy were employed for characterizations. Upon hydrolysis, polydiacetylene esters in the cellulosic fiber matrix were found unaffected by hydrolysis treatment, which made the composites suitable for OP sensing. Furthermore, the nanofibrous (NF) composites exhibited tensile properties suitable to be used as a textile material. Finally, the NF composites exhibited colorimetric sensing of OP, which is visible to the naked eye. This research is a landmark study toward the development of OP sensing in a protective clothing system.

scholarly journals Synthesis and Characterizations of Dipeptide Derivative of Gentamicin

2019 ◽  
Vol 28 (2) ◽  
pp. 73-82
Author(s):  
Oun D. Khudair ◽  
Diar A. Fatih
Keyword(s):  
Acid Chloride ◽  
Solution Method ◽  
Hydroxyl Group ◽  
Hydroxyl Groups ◽  
Free Hydroxyl ◽  
Ester Linkage ◽  
Amine Groups ◽  
Conventional Solution ◽  
Dipeptide Derivative

Abstract       The target derivative are gentamicin linked with L-Val- L-Ala by an ester linkage. These were synthesized by esterification method, which included the reaction of -OH hydroxyl group on (carbon No.5) of gentamicin with the acid chloride of the corresponding dipeptide, The preparation of new derivative of gentamicin involved protected the primary & secondary amine groups of Gentamicin, by Ethylchloroformate (ECF) to give N-carbomethoxy Gentamicin which was used for further chemical synthesis involving the free hydroxyl groups. Then prepared dipeptide (L-Val- L-Ala) by conventional solution method in present DCC & HoBt then reacted with thionyl chloride to prepared acid chloride of dipeptides, then after, linked by ester linkage to N-protection gentamicin in present pyridine as base, finally deportation the amino group of synthesized compound by using TFAA in present anisole. The characterization of the titled compounds were performed utilizing FTIR spectroscopy, CHNS elemental analysis, and by measurements of their physical properties.  

Synthesis and Characterization of an Alendronate-Chitosan Conjugate

2011 ◽  
Vol 140 ◽  
pp. 53-57 ◽  
Author(s):  
Xiao Hong Shao ◽  
Ji Qing Xu ◽  
Yan Peng Jiao ◽  
Chang Ren Zhou
Keyword(s):  
Drug Delivery ◽  
Drug Delivery System ◽  
Synthesis And Characterization ◽  
Hydroxyl Groups ◽  
Amino Groups ◽  
H Nmr ◽  
Ft Ir ◽  
Novel Drug Delivery System ◽  
Novel Drug

The biomineral-binding alendronate-chitosan conjugate (Scheme 1) was developed as a novel drug delivery system. Alendronate was conjugated to the hydroxyl groups of chitosan, thereby maintaining the amino groups of chitosan intact. By means of FT-IR and 1H NMR, the characterization was conducted to confirm the successful synthesis of alendronate-chitosan conjugate.

scholarly journals Characterization of Ionic Liquid Lignins Isolated from Spruce Wood with 1-Butyl-3-methylimidazolium Acetate and Methyl Sulfate and Their Binary Mixtures with DMSO

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2479 ◽  
Author(s):  
Artyom V. Belesov ◽  
Anton V. Ladesov ◽  
Ilya I. Pikovskoi ◽  
Anna V. Faleva ◽  
Dmitry S. Kosyakov
Keyword(s):  
Ionic Liquids ◽  
Binary Mixtures ◽  
Plant Biomass ◽  
High Resolution Mass Spectrometry ◽  
Covalent Binding ◽  
Structural Features ◽  
Size Exclusion ◽  
Hydroxyl Groups ◽  
Spruce Wood

Ionic liquids (ILs) based on 1-butyl-3-methylimidazolium (bmim) cation have proved to be promising solvents for the fractionation of plant biomass with the production of cellulose and lignin. This study deals with the characterization of lignins isolated from coniferous (spruce) wood using [bmim]OAc and [bmim]MeSO4 ionic liquids and their binary mixtures with DMSO (80:20). Molecular weight distributions, functional composition, and structural features of IL lignins were studied by size-exclusion chromatography, NMR spectroscopy (1D and 2D) and atmospheric pressure photoionization high-resolution mass spectrometry. It was shown that the interaction of ILs with lignin leads to significant chemical changes in the biopolymer; a decrease in the degree of polymerization and in the content of free phenolic hydroxyl groups due to alkylation, the disappearance (in the case of [bmim]OAc) of carbonyl groups and a significant destruction of β-O-4 bonds. The chemical reactions between lignin and 1-butyl-3-methylidazolium cation with covalent binding of ionic liquids or products of their decomposition is evidenced by the presence of a large number of nitrogen-containing oligomers in IL lignins.

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