Redox active metal-sulfide clusters and computer-assisted instructional lessons on transition metal chemistry
Gammon, Steven Drew
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Permalink
https://hdl.handle.net/2142/20930
Description
Title
Redox active metal-sulfide clusters and computer-assisted instructional lessons on transition metal chemistry
Author(s)
Gammon, Steven Drew
Issue Date
1989
Doctoral Committee Chair(s)
Smith, Stanley
Department of Study
Chemistry
Discipline
Chemistry
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Chemistry, Inorganic
Education, Teacher Training
Education, Technology of
Language
eng
Abstract
The chemical education research was focused on the design and implementation of a series of interactive videodisc chemistry lessons. These lessons were designed to give first year chemistry students an appreciation of some of the structural and electronic issues of coordination chemistry. This software uses IBM personal computers, Pioneer and Sony videodisc players, both touch and non-touch screens, and a local area network. The programming was done in Microsoft QuickBASIC. The videodisc was used in these lessons as a means for the students to observe real reactions of some transition metal complexes. The videodisc was also used to present a unique teaching approach to complementary colors and d orbital splitting of octahedral complexes.
The synthetic inorganic chemistry research involved the synthesis and characterization of a series of charge transfer salts using metal sulfide clusters and TCNQ. The goal of the research was to design a group of salts to be the organometallic analogs of (TTF)(TCNQ) and demonstrate metallic conductivity.
The metal sulfide clusters were cubanes of the formula (RCp)$\sb4$M$\sb2$M$\sp\prime\sb2$S$\sb4$ (R = H, Cp; M = Cr, V; M$\sp\prime$ = Cr,V) and the cluster (RCp)$\sb5$V$\sb5$S$\sb6$ (R = H, Cp). All of the above clusters were examined by cyclic voltammetry and were found to have a 0/+1 oxidation wave at about 0 mV (Ag/AgCl). This oxidation made them suitable for reaction with TCNQ. Upon reaction with TCNQ, we found that these clusters formed both 1:1 (cluster:TCNQ) and 1:2 charge transfer salts with TCNQ. These compounds were semiconductors with band gaps in the range of 0.24-0.75 eV. IR and structural studies of both the 1:1 and 1:2 indicated that the TCNQ had undergone a Peierls distortion and was dimerized.
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