De novo synthesis of gem-dialkyl chlorophyll analogues for probing and emulating our green world
about
Strong Coupling of Localized Surface Plasmons to Excitons in Light-Harvesting Complexes.Bioconjugatable, PEGylated Hydroporphyrins for Photochemistry and Photomedicine. Narrow-Band, Red-Emitting Chlorins.Modifications of Porphyrins and Hydroporphyrins for Their Solubilization in Aqueous Media.Photophysical Characterization of the Naturally Occurring Dioxobacteriochlorin Tolyporphin A and Synthetic Oxobacteriochlorin Analogues.Design and engineering of water-soluble light-harvesting protein maquettes.Furan- and Thiophene-Based Auxochromes Red-shift Chlorin Absorptions and Enable Oxidative Chlorin Polymerizations.Synthesis and Spectral Properties of meso-Arylbacteriochlorins, Including Insights into Essential Motifs of their Hydrodipyrrin Precursors.Quantitation of Tolyporphins, Diverse Tetrapyrrole Secondary Metabolites with Chlorophyll-Like Absorption, from a Filamentous Cyanobacterium-Microbial Community.Chlorophyll-Inspired Red-Region Fluorophores: Building Block Synthesis and Studies in Aqueous Media.Amphiphilic BODIPY-Hydroporphyrin Energy Transfer Arrays with Broadly Tunable Absorption and Deep Red/Near-Infrared Emission in Aqueous Micelles.Assembling Porphyrins into Extended Network Structures by Employing Aromatic Dicarboxylates: Synthesis, Metal Exchange, and Heterogeneous Catalytic Studies.β-Alkyloxazolochlorins: Revisiting the Ozonation of Octaalkylporphyrins, and Beyond.Oxidations of chromene-annulated chlorins.Tolyporphin-An Unusual Green Chlorin-like Dioxobacteriochlorin.NIR bacteriochlorin chromophores accessed by Heck and Sonogashira cross-coupling reactions on a tetrabromobacteriochlorin derivative.Synthesis of tailored hydrodipyrrins and their examination in directed routes to bacteriochlorins and tetradehydrocorrinsCharacterization of Hydroporphyrins Covalently Attached to Si(100)Synthesis, photophysics and electronic structure of oxobacteriochlorinsSynthesis and photophysical characteristics of 2,3,12,13-tetraalkylbacteriochlorinsPhotophysical comparisons of PEGylated porphyrins, chlorins and bacteriochlorins in waterPanchromatic chromophore–tetrapyrrole light-harvesting arrays constructed from Bodipy, perylene, terrylene, porphyrin, chlorin, and bacteriochlorin building blocksCopper-Porphyrin-Metal-Organic Frameworks as Oxidative Heterogeneous CatalystsAn easily accessible and recyclable copper nanoparticle catalyst for the solvent-free synthesis of dipyrromethanes and aromatic amines
P2860
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P2860
De novo synthesis of gem-dialkyl chlorophyll analogues for probing and emulating our green world
description
2015 nî lūn-bûn
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2015 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
name
De novo synthesis of gem-dialk ...... and emulating our green world
@ast
De novo synthesis of gem-dialk ...... and emulating our green world
@en
De novo synthesis of gem-dialk ...... and emulating our green world
@nl
type
label
De novo synthesis of gem-dialk ...... and emulating our green world
@ast
De novo synthesis of gem-dialk ...... and emulating our green world
@en
De novo synthesis of gem-dialk ...... and emulating our green world
@nl
prefLabel
De novo synthesis of gem-dialk ...... and emulating our green world
@ast
De novo synthesis of gem-dialk ...... and emulating our green world
@en
De novo synthesis of gem-dialk ...... and emulating our green world
@nl
P2860
P3181
P1433
P1476
De novo synthesis of gem-dialk ...... and emulating our green world
@en
P2093
Jonathan S. Lindsey
P2860
P304
P3181
P356
10.1021/ACS.CHEMREV.5B00065
P407
P577
2015-07-08T00:00:00Z