Journal ArticleDOI
Synthesis and photophysical properties of chiral dendrimers with quinoline surface group via click chemistry
Perumal Rajakumar,Rathinam Raja +1 more
TLDR
In this paper, the synthesis of chiral dendrimers containing quinoline as surface group and 1 2,3-triazole as branching unit is described, and the photophysical properties indicate an increase in the molar extinction coefficient and fluorescence intensity and a decrease in quantum yield and lifetime as the generation of the dendromer increases.About:
This article is published in Tetrahedron Letters.The article was published on 2010-08-18. It has received 24 citations till now. The article focuses on the topics: Dendrimer & Quinoline.read more
Citations
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Journal ArticleDOI
Dendritic effects: dependency of dendritic nano-periodic property patterns on critical nanoscale design parameters (CNDPs)
TL;DR: Dendritic effects as the authors now know them can be viewed as collections of “mini nano-periodic property patterns” that may ultimately be used to frame and define a broader encompassing Mendeelev-like system for the a priori prediction of dendritic polymer properties.
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Copper in dendrimer synthesis and applications of copper–dendrimer systems in catalysis: a concise overview
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Synthesis and DSSC application of novel dendrimers with benzothiazole and triazole units
TL;DR: In this paper, the authors showed that the presence of more number of benzothiazole and triazole units increases the molar absorption coefficient and alters the fluorescence as well as electrochemical behaviors in the dendrimers.
Journal ArticleDOI
Synthesis, crystal structure, ABTS radical-scavenging activity, antimicrobial and docking studies of some novel quinoline derivatives
Sumaiya Tabassum,T.H. Suresha Kumara,Jerry P. Jasinski,Sean P. Millikan,Hemmige S. Yathirajan,P. S. Sujan Ganapathy,H.B.V. Sowmya,Sunil S. More,Gopalpur Nagendrappa,Manpreet Kaur,Gilish Jose +10 more
TL;DR: In this article, a series of 9 2-chloroquinolin-3-yl ester derivatives have been synthesized via a two-step protocol from 2-Chloroquinoline 3-carbaldehyde.
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Synthesis of chiral core based triazole dendrimers with m-terphenyl surface unit and their antibacterial studies
TL;DR: S-BINOL based chiral dendrimers with m-terphenyl at the surface and triazole as the bridging unit with antibacterial activity against Shigella dysenteriae, Staphylococcus aureus and Serratia marcescen are synthesized by a convergent synthetic strategy through the 'click' chemistry approach.
References
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Journal ArticleDOI
Click Chemistry: Diverse Chemical Function from a Few Good Reactions.
TL;DR: In this paper, a set of powerful, highly reliable, and selective reactions for the rapid synthesis of useful new compounds and combinatorial libraries through heteroatom links (C-X-C), an approach called click chemistry is defined, enabled, and constrained by a handful of nearly perfect "springloaded" reactions.
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Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides.
TL;DR: A novel regiospecific copper(I)-catalyzed 1,3-dipolar cycloaddition of terminal alkynes to azides on solid-phase is reported, and the X-ray structure of 2-azido-2-methylpropanoic acid has been solved, to yield structural information on the 1, 3-dipoles entering the reaction.
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Dendrimers in biomedical applications--reflections on the field.
Sonke Svenson,Donald A. Tomalia +1 more
TL;DR: The reflections on biomedical applications of dendrimers given in this review clearly demonstrate the potential of this new fourth major class of polymer architecture and indeed substantiate the high hopes for the future of dendedrimers.
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Bioconjugation by Copper(I)-Catalyzed Azide-Alkyne [3 + 2] Cycloaddition
TL;DR: The copper-catalyzed cycloaddition reaction between azides and alkynes functions efficiently in aqueous solution in the presence of a tris(triazolyl)amine ligand to make rapid and reliable covalent connections to micromolar concentrations of protein decorated with either of the reactive moieties.
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Functional polymers and dendrimers: reactivity, molecular architecture, and interfacial energy
TL;DR: The interaction of polymers with their environment depends largely on the functional groups they carry and the placement of functional groups at polymer chain ends or in well-defined segments can determine the ultimate properties.