Sentence examples for moiety is linked from inspiring English sources
An intramolecular charge transfer (ICT) fluorescent probe, in which the thiourea derivative moiety is linked to the fluorescent 4- dimethylamino) benzamide, has been designed and synthesized.
We report on the synthesis of some novel liquid crystalline polyacetylenes derived from monosubstituted acetylenic monomers where the acetylenic moiety is linked through a short spacer (one or three methylene units and an ether bridge) to a biphenyl mesogenic core.
O(11) – H(11) group of cation moiety is linked through hydrogen bonding to O 8) of the carbonyl group of anion and O(10) – H(10) of cation moiety is also linked through hydrogen bonding to O 9) of the carbonyl group of anion.
Steven et al. [26, 27] define a CGC as "a complex in which a π-bonded moiety is linked to one of the other ligands on the same metal centre in such a way that the angle measured between the centroid of the π-system and the additional ligand is smaller than the comparable unbridged complex".
The TFO moiety is linked in 5' through a scissile S-S bond to 4,5',8-trimethylpsoralen and in 3' to biotin TEG.
This anchor moiety is linked to the hemopexin-like domain by a 35 45 amino acid long hydrophilic linker, or stem.
This moiety was linked to C-2 as indicated by HMBC correlations from the anomeric proton (δ H 4.44) to C-2 (δ C 72.6).
A pro-drug (labeled 1) where naloxone and the indolequinone moiety were linked through a carbonate bond was rapidly hydrolyzed in phosphate buffered saline.
The piperidinyl moiety was linked to C-16 through C-16 C-17 C-16 C-17 C-16 C-17ations from H-16 to C-17 and C-22 and 1H-1H COSY correlation of H-16/H-17 (Fig. 1).
In a continuing study of hybrid compounds containing the α-bromoacryloyl moiety as potential anticancer drugs, we synthesized a novel series of hybrids 4a h, in which this moiety was linked to a 1,5-diaryl-1,4-pentadien-3-one system.
A series of N-aryl heteroarylisopropanolamines in which an indole or a 3-arylpyrrole moiety was linked to an aryl group through an isopropanolamine linker, were designed and synthesized as potential anti-HIV-1-PR agents.
