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We examined the potential of a series of aromatic moieties with different electron-donating ability to alter SWCNT electronic properties.
These ligands are derived from d-glucosamine and contain several substituents in the biphenyl moieties, with different steric and electronic properties.
Three new organic small molecules (TPA-DTBT, TPA-DTBT-TH and TPA-DTBT-CAO) containing triphenylamine (TPA) and 4,7-bis(thiophen-2-yl benzo[1,2,5]thiadiazole thiophen-2-yl benzo[1,2,5]thiadiazoleal thiophen-2-yl benzo[1,2,5]thiadiazole
Ten 1-phenyl-1H-pyrazolo[3,4-b]pyridine 1-phenyl-1H-pyrazolo[3,4-b]pyridine 1-phenyl-1H-pyrazolo[3,4-b]pyridine 1-phenyl-1H-pyrazolo[3,4-b]pyridine 1-phenyl-1H-pyrazolo[3,4-b]pyridineederivativeslasmodium falconnected
In our effort to develop potent anti-hyperglycemic agents with potential agonistic activities toward PPARγ and SUR, three novel series of quinoxaline derivatives bearing sulfonylurea or sulfonylthiourea moieties with different linkers were designed and synthesized.
Three novel organic sensitizers were molecularly designed and synthesized based on triphenylamine (TPA), as the core donor (DTPA), linked to one, two or three carbazole (DCarb) moieties with different number of anchoring groups (AG) to generate: DTPA-π-DCarb-A (DE1), DTPA π-DCarb-A 2 (DTPA π-DCarb-A 2-DTPA π-DCarb-A 2.
Similar(53)
The ferrocenyl moiety with different spacer groups acts as donor and 1,3,5-triazine as acceptor.
Three cholesterol derivatives containing an azobenzene moiety with different polarities were designed and synthesized (AB lipids 1 to 3).
The designed compounds possess the previously described exigencies for optimal anti-parasite activity, the 5-ethenylbenzofuroxanyl moiety with different substituents.
A series of novel novolac epoxy resins containing naphthalene moiety with different molecular weights were synthesized via condensation of bisphenol A and 1-naphthaldehyde, followed by epoxidation with epichlorohydrin.
To further understand the structure-function relationship of these Fe(II -form selectII -formP inhibitorselectivees of catechol derivatives was designed and synthesized by replaceMetAPof the thinhibitorsthiophene moiety with different five-membered and seriesmbered heterofycatechol
Related(20)
sections with different
fractions with different
portions with different
segments with different
groups with different
moieties with distinct
clusters with different
periods with different
moieties with various
pieces with different
sides with different
cartons with different
moieties with differing
moieties with varying
sizes with different
moieties with chiral
moieties with hydroxyl
moieties with secondary
moieties with hydrophobic
moieties with sulfur-containing
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