181725-37-1Relevant academic research and scientific papers
Functionalized biodegradable triclosan monomers and oligomers for controlled release
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Page/Page column 52, (2011/11/13)
This invention relates to the discovery of functionalized triclosan monomers and oligomers that, when incorporated into a substrate of, or applied as part of a coating to, medical devices and/or consumer products may extend the duration of antimicrobial properties to the medical devices and/or consumer products.
FUNCTIONALIZED BIODEGRADABLE TRICLOSAN MONOMERS AND OLIGOMERS FOR CONTROLLED RELEASE
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, (2009/05/29)
This invention relates to the discovery of functionalized triclosan monomers and oligomers that, when incorporated into a substrate of, or applied as part of a coating to, medical devices and/or consumer products may extend the duration of antimicrobial properties to the medical devices and/or consumer products.
Structure-reactivity relationship in interlocked molecular compounds and in their supramolecular model complexes
Asakawa, Masumi,Brown, Christopher L.,Menzer, Stephan,Raymo, Fran?isco M.,Stoddart, J. Fraser,Williams, David J.
, p. 2614 - 2627 (2007/10/03)
Examination of the pseudorotaxane-like geometries adopted in the solid state by a series of 1:1 complexes revealed significant differences in the hydrogen bonding interactions between oxygen atoms in some hydroquinone-based guests carrying polyether/polye
Syntheses of ligands containing two and three 2,2'-(bisamino)diphenyl ether units designed for molecular self-assembly on lithiation
Ashton, Peter R.,H?rner, Bernd,Kocian, Oldrich,Menzer, Stephan,White, Andrew J. P.,Stoddart, J. Fraser,Williams, David J.
, p. 930 - 940 (2007/10/03)
The syntheses of polyamines containing two or three 2,2'-(bisamino)diphenyl ether units linked together, designed for self-assembly following lithiation, are reported. The X-ray crystal structures of two of the bis[2,2'-(bisamido)diphenyl ethers] are described. The ligand, which is linked by an ethylene glycol spacer, exhibits a coiled conformation constrained by intramolecular hydrogen bonds and supplemented by [CH-π] interactions. The ligand, which is linked by a more rigid bridge, containing a paraphenylene unit, displays a stretched conformation stabilised by intramolecular hydrogen bonds and intramolecular T-type aromatic-aromatic edge-to-face interactions.
