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dc.contributor.authorKomreddy, Venugopal R.
dc.contributor.authorRillema, D. Paul
dc.contributor.authorNguyen, Huy A.
dc.contributor.authorCruz, Arvin
dc.contributor.authorMoore, Curtis E.
dc.contributor.authorSenaratne, Nilmini
dc.contributor.authorKadel, Lava R.
dc.contributor.authorEichhorn, David M.
dc.identifier.citationKomReddy, Venugopal; Rillema, D.; Nguyen, Huy; Cruz, Arvin; Moore, Curtis; Senaratne, Nilmini; Kadel, Lava; Eichhorn, David From Abstracts of Papers, 255th ACS National Meeting & Exposition, New Orleans, LA, United States, March 18-22, 2018 (2018), INOR-870en_US
dc.descriptionClick on the URI to access the article (may not be free).en_US
dc.description.abstractGeneral synthetic methods have been devised to prep. derivatized mixed-​ring heterocyclic and antenna carotene ligands with nitrogen donor atoms. Synthetic methods involve prepn. of intermediate compds. in route to arom. heterocyclic products with bidentate and monodentate coordination sites. Coupling reactions resulted in formation of the mixed-​ring heterocycles whereas condensation reactions of carotene aldehydes with org. mols. lacking beta hydrogen atoms formed ligands with either pyridine and​/or cyanide linkages. Further, condensation reactions have been used to prep. uracil​/multidentate ligand motifs. The ligands were characterized by elemental analyses, NMR and single x-​ray diffraction methods. These ligands are being used to prep. organometallic complexes for solar energy and therapeutic purposes.en_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.ispartofseriesAbstracts of Papers of the American Chemical Society;v.255
dc.titleDerivatized mixed-ring heterocyclic and antenna carotene ligandsen_US
dc.rights.holder© 2018 American Chemical Society. All Rights Reserved.en_US

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