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AuthorMengele, Alexanderdc.contributor.author
AuthorRau, Svendc.contributor.author
Date of accession2021-12-09T09:21:25Zdc.date.accessioned
Available in OPARU since2021-12-09T09:21:25Zdc.date.available
Date of first publication2017-05-25dc.date.issued
AbstractDue to the limited amount of fossil energy carriers, the storage of solar energy in chemical bonds using artificial photosynthesis has been under intensive investigation within the last decades. As the understanding of the underlying working principle of these complex systems continuously grows, more focus will be placed on a catalyst design for highly selective product formation. Recent reports have shown that multifunctional photocatalysts can operate with high chemoselectivity, forming different catalysis products under appropriate reaction conditions. Within this context [(bpy)Rh(Cp*)X]n+-based catalysts are highly relevant examples for a detailed understanding of product selectivity in artificial photosynthesis since the identification of a number of possible reaction intermediates has already been achieved.dc.description.abstract
Languageendc.language.iso
PublisherUniversität Ulmdc.publisher
LicenseCC BY 4.0 Internationaldc.rights
Link to license texthttps://creativecommons.org/licenses/by/4.0/dc.rights.uri
Keywordartificial photosynthesisdc.subject
Keywordproduct selectivitydc.subject
Keywordreaction mechanismdc.subject
Dewey Decimal GroupDDC 540 / Chemistry & allied sciencesdc.subject.ddc
LCSHReaction mechanisms (Chemistry)dc.subject.lcsh
TitleProduct selectivity in homogeneous artificial photosynthesis using [(bpy)Rh(Cp*)X]n+-based catalystsdc.title
Resource typeWissenschaftlicher Artikeldc.type
SWORD Date2020-01-28T13:27:08Zdc.date.updated
VersionpublishedVersiondc.description.version
DOIhttp://dx.doi.org/10.18725/OPARU-40293dc.identifier.doi
URNhttp://nbn-resolving.de/urn:nbn:de:bsz:289-oparu-40369-5dc.identifier.urn
GNDRhodiumdc.subject.gnd
FacultyFakultät für Naturwissenschaftenuulm.affiliationGeneral
InstitutionInstitut für Anorganische Chemie I (Materialien und Katalyse)uulm.affiliationSpecific
Peer reviewjauulm.peerReview
DCMI TypeTextuulm.typeDCMI
CategoryPublikationenuulm.category
DOI of original publication10.3390/inorganics5020035dc.relation1.doi
Source - Title of sourceInorganicssource.title
Source - Place of publicationMDPIsource.publisher
Source - Volume5source.volume
Source - Issue2source.issue
Source - Year2017source.year
Source - Article number35source.articleNumber
Source - eISSN2304-6740source.identifier.eissn
Bibliographyuulmuulm.bibliographie


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