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Synthesis

Trinity University

Publication Year

Articles 1 - 3 of 3

Full-Text Articles in Chemistry

Cucurbit[8]Uril Rotaxanes, Vijayakumar Ramalingam, Adam R. Urbach Sep 2011

Cucurbit[8]Uril Rotaxanes, Vijayakumar Ramalingam, Adam R. Urbach

Chemistry Faculty Research

The synthesis of [2]rotaxanes, each comprising a viologen core threaded through a cucurbit[8]uril (Q8, Figure 1) macrocycle and stoppered by tetraphenylmethane groups, and their binding to second guests as inclusion complexes in organic and aqueous media are described. Stoppering was observed to have little effect on binding. Chemical modification of the threaded guest was used to control solubility and binding characteristics, thus demonstrating a novel approach to making artificial receptors with readily modifiable properties.


Antiaromatic Dianions: Dianions Of Dixanthylidene By Reduction And Attempted Excited-State Deprotonation, Mary Black, Clifford Woodford, Nancy S. Mills Jan 2011

Antiaromatic Dianions: Dianions Of Dixanthylidene By Reduction And Attempted Excited-State Deprotonation, Mary Black, Clifford Woodford, Nancy S. Mills

Chemistry Faculty Research

Reduction of dixanthylidene with potassium or lithium resulted in formation of the antiaromatic dianion in high yield. Attempts to form the dianion by excited-state deprotonation of dixanthene with n-butyllithium/TMEDA resulted in formation of the tetraanion from deprotonation ortho to the oxygen. Orientation of the sp3 hydrogens presumably allows preferential deprotonation of the xanthene rings.


Air And Water Free Solid-Phase Synthesis Of Thiol Stabilized Au Nanoparticles With Anchored, Recyclable Dendrimer Templates, John D. Gilbertson, G. Vijayaraghavan, K. J. Stevenson, Bert D. Chandler Jan 2007

Air And Water Free Solid-Phase Synthesis Of Thiol Stabilized Au Nanoparticles With Anchored, Recyclable Dendrimer Templates, John D. Gilbertson, G. Vijayaraghavan, K. J. Stevenson, Bert D. Chandler

Chemistry Faculty Research

Solid-phase synthetic templates for Au nanoparticles were developed using Merrifield resins and polyamidoamine (PAMAM) dendrimers. This synthetic scheme affords the opportunity to prepare metal nanoparticles in the absence of air and water, and it does not necessitate phase transfer agents that can be difficult to remove in subsequent steps. Amine-terminated generation 5 PAMAM (G5NH2) dendrimers were grafted to anhydride functionalized polystyrene resin beads and alkylated with 1,2-epoxydodecane to produce G5C12anch. The anchored dendrimers bound both CoII and AuIII salts from toluene solutions at ratios comparable to those of solution phase alkyl-terminated PAMAM dendrimers. The encapsulated AuIII salts could be reduced …