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Multimetallic complexes supported by ligands with Pyridine6-​X3 donor sets

De Ruiter, Graham and Agapie, Theodor (2014) Multimetallic complexes supported by ligands with Pyridine6-​X3 donor sets. In: 248th American Chemical Society National Meeting & Exposition, August 10-14, 2014, San Francisco, CA. http://resolver.caltech.edu/CaltechAUTHORS:20140812-110442326

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Abstract

The biochem. processing of a wide variety of gasses including, H_2, N_2, CO_2, CO and NO_x requires complex machinery. Anaerobic metalloenzymes are highly specialized in such transformations, and often employ multi-metal cooperativity. A bio-inspired approach to tackle energy related problems involving CO_2 and N_2, for instance, is appealing. However controlling the assembly of multiple metals into a single organized framework remains a challenge. Recently we demonstrated that a multidentate ligands can support clusters that mimic the structural topol. of the oxygen evolving complex (OEC) in photosystem II (PSII).[2] This ligand framework consisting of a 1, 3,5-triarylbenzene core decorated with dipyridyl-alc. moieties supports a large variety of metal clusters.] Towards expanding the scope of our previously prepd. clusters, we utilized N/S donors or all N-type donors in new ligand designs. The coordination modes with first-row transition metals and the reactivity of these multimetallic complexes will be discussed.


Item Type:Conference or Workshop Item (Paper)
Related URLs:
URLURL TypeDescription
http://www.acs.org/content/acs/en/meetings/fall-2014.htmlOrganizationConference Website
ORCID:
AuthorORCID
Agapie, Theodor0000-0002-9692-7614
Additional Information:© 2014 American Chemical Society.
Record Number:CaltechAUTHORS:20140812-110442326
Persistent URL:http://resolver.caltech.edu/CaltechAUTHORS:20140812-110442326
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:48378
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:12 Aug 2014 18:33
Last Modified:05 May 2017 20:22

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