Works (4)
Updated: July 5th, 2023 15:54
2015 journal article
Photophysical Properties and Electronic Structure of Chlorin-Imides: Bridging the Gap between Chlorins and Bacteriochlorins
JOURNAL OF PHYSICAL CHEMISTRY B, 119(24), 7503–7515.
Contributors: K. Faries *, J. Diers *, J. Springer*, E. Yang*, M. Ptaszek n, n, M. Krayer n, M. Taniguchi n
MeSH headings : Electrons; Fluorescence; Imides / chemistry; Molecular Structure; Photochemical Processes; Porphyrins / chemistry; Quantum Theory
TL;DR:
The photophysical properties of a set of six chlorin-imides and nine synthetic chlorin analogues that extend the absorption deeper into these key spectral regions of the solar spectrum and help bridge the gap between typical chlorins and bacteriochlorins are reported.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
7. Affordable and Clean Energy
(OpenAlex)
Sources: Web Of Science, NC State University Libraries, ORCID
Added: August 6, 2018
2010 journal article
De Novo Synthesis of Long-Wavelength Absorbing Chlorin-13,15-dicarboximides
JOURNAL OF ORGANIC CHEMISTRY, 75(5), 1659–1673.
TL;DR:
The synthetic versatility of the de novo route complements the existing semisynthetic route from chlorophylls and should enable fundamental spectroscopic studies and photochemical applications.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
6. Clean Water and Sanitation
(OpenAlex)
Sources: Web Of Science, NC State University Libraries
Added: August 6, 2018
2009 journal article
Regioselective Bromination Tactics in the de Novo Synthesis of Chlorophyll b Analogues
JOURNAL OF ORGANIC CHEMISTRY, 74(9), 3237–3247.
Contributors: C. Muthiah n, n, M. Taniguchi n , M. Ptaszek n & J. Lindsey n
MeSH headings : Chlorophyll / chemical synthesis; Chlorophyll / chemistry; Halogenation; Porphyrins / chemistry; Spectrum Analysis; Stereoisomerism; Substrate Specificity
TL;DR:
Taken together, the facile access to chlorins and 13(1)-oxophorbines bearing substituents at distinct sites should enable fundamental spectroscopic studies and diverse applications.
(via Semantic Scholar)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, NC State University Libraries, ORCID
Added: August 6, 2018
2007 review
Design and synthesis of manganese porphyrins with tailored lipophilicity: Investigation of redox properties and superoxide dismutase activity
[Review of ]. BIOORGANIC & MEDICINAL CHEMISTRY, 15(22), 7066–7086.
author keywords: porphyrin; porphodimethene; manganese; lipophilic; amphipathic; cyclic voltammetry; superoxide dismutase
MeSH headings : Catalysis; Cytochromes c / chemistry; Drug Design; Electrochemistry; Electron Transport; Enzyme Activation / drug effects; Lipid Bilayers / chemistry; Manganese / chemistry; Metalloporphyrins / chemical synthesis; Metalloporphyrins / chemistry; Molecular Structure; Oxidation-Reduction; Solubility; Stereoisomerism; Structure-Activity Relationship; Superoxide Dismutase / chemistry; Superoxides / chemistry
TL;DR:
Thirteen new manganese porphyrins and two porphodimethenes bearing one to three different substituents at the meso positions in a variety of architectures have been synthesized, and the superoxide dismutase activity of the compounds has been examined.
(via Semantic Scholar)
open access via europepmc.org (repository)
UN Sustainable Development Goal Categories
3. Good Health and Well-being
(Web of Science)
Sources: Web Of Science, NC State University Libraries
Added: August 6, 2018
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