Results 51 to 60 of about 74,679 (236)

Bulk Polymerization Kinetics of Hydroxy Terminated Polybutadiene and Toluene Diisocyanate with Infrared Spectroscopy

open access: yesIndonesian Journal of Chemistry, 2018
A study on bulk polymerization kinetics of HTPB (Hydroxy Terminated Polybutadiene) and TDI (Toluene Diisocyanate) with infrared (IR) spectroscopy has been conducted.
Heri Budi Wibowo   +2 more
doaj   +1 more source

Synthesis and crystal structure of [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](isocyanato-κN)gold(I)

open access: yesActa Crystallographica Section E: Crystallographic Communications
The title complex, [Au(NCO)(C27H36N2)], was synthesized by ligand metathesis from [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]gold(I) chloride and sodium cyanate in anhydrous tetrahydrofuran and crystallized from toluene at 233 K in the ...
Abolghasem Bakhoda
doaj   +1 more source

Developing an Efficient and General Strategy for Immobilization of Small Molecules onto Microarrays Using Isocyanate Chemistry

open access: yesSensors, 2016
Small-molecule microarray (SMM) is an effective platform for identifying lead compounds from large collections of small molecules in drug discovery, and efficient immobilization of molecular compounds is a pre-requisite for the success of such a platform.
Chenggang Zhu   +8 more
doaj   +1 more source

Anomeric Amide Enabled Divergent Synthesis of Unsymmetrical Ureas, Carbamates, Thioesters, and Amides From Aldehydes

open access: yesAngewandte Chemie International Edition, EarlyView.
An anomeric amide‐enabled divergent aldehyde functionalization sequence provides one‐pot access to unsymmetrical ureas, carbamates, thiocarbamates, thioesters, and amides. Key to this transformation is the formation of N‐Boc‐hydroxamate intermediates, which serve as platforms for orthogonal activation via Lossen‐type rearrangements, single‐electron ...
Jasper L. Tyler   +6 more
wiley   +1 more source

Supramolecular protection of isocyanates from water by encapsulation within hydrophobic crystalline pillar[n]arene macrocycles

open access: yesNature Communications
The high reactivity of isocyanate groups not only makes them excellent precursors for polyurethanes and polyureas, but it also leads to their degradation through reactions with atmospheric moisture. Conventionally, blocking reagents containing alcohol or
Kiichi Yasuzawa   +8 more
doaj   +1 more source

Determination of phenylurethane and isocyanate groups in isocyanates

open access: yes, 2020
Reactions of phenylurethane and isocyanate groups of arylisocyanates with secondary amines are studied by IR spectrometry and potentiometric titration. It is found that the rate of the reaction between isocyanate groups and diethylamine is nearly independent of the solvent nature.
Evtushenko Yu.M.   +2 more
openaire   +1 more source

Thermal Black‐Infused Polyurethane Rigid Foams: Novel Formulations Toward Higher‐Performance and More Sustainable Insulation

open access: yesJournal of Applied Polymer Science, EarlyView.
Thermal black improves polyurethane foam structure and stability. It helps the foam rise smoothly while promoting the formation of smaller, more uniform cells. The foam keeps its strength and insulation performance while reducing shrinkage. Its clean production and easy processing make it a sustainable, cost‐effective option for high‐performance ...
Mihaela Mihai   +3 more
wiley   +1 more source

Rapid Determination of Residues and Migration of Seven Isocyanate Compounds in Food Composite Packaging Bags by Ultra-high Performance Convergence Chromatography [PDF]

open access: yesShipin Kexue
An ultra-high performance convergence chromatography (UPC2) method was developed to rapidly determine the residues and migration of seven isocyanate compounds in food composite packaging bags.
QIU Yue, LI Genrong, YU Qiuling, TAN Chaolan, LU Jiali, ZHANG Qing
doaj   +1 more source

isocyanates [PDF]

open access: yes, 2014
Citation: 'isocyanates' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.I03269 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

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