<!--This file created 4/30/97 12:38 PM by Claris Home Page version 1.0--><HTML><HEAD>   <TITLE>CHEMISTRY -- Dr Cammarata</TITLE>   <META NAME=GENERATOR CONTENT="Claris Home Page 1.0">   <X-SAS-WINDOW TOP=66 BOTTOM=480 LEFT=8 RIGHT=538></HEAD><BODY><H1 ALIGN=CENTER>Auburn University - Chemistry</H1><H1 ALIGN=CENTER>Dr. Vince Cammarata - Research</H1><P ALIGN=CENTER>&nbsp;</P><P><IMG SRC="Vince1.jpg" WIDTH=198 HEIGHT=252 X-SAS-UseImageWidthX-SAS-UseImageHeight ALIGN=bottom></P><H2>Vince Cammarata, Ph.D. - Massachusetts Institute of Technology -1989 B.S. CalTech- 1983</H2><P>My research centers on making and understanding the physicalproperties of materials applicable to nanomolecular devices. Thechallenge lies in assembling molecules on surfaces and understandingthe behavior of 1-, 2- and thin 3-dimensional (1-, 2- and thin 3-D)materials. The ultimate goal is to build surface structures withspecial optical and electronic properties, such as the ability toconvert electrons to photons through electrochemiluminescence (ECL)</P><P>Thin 3-D layered materials are formed by stacking simpler pieces,i.e. 2-D monolayers or the electrosynthesis of surface boundpolymers. The monolayer approach uses an interface to align andorient individual molecules into close-packed single molecule thicklayers. These macromolecular layers are stacked using a combinationof evaporation, self-assembly and/or Langmuir-Blodgett techniques.While most researchers have used saturated hydrocarbons to producemonolayers, my research has shown the ability of rigid rod aromaticmolecules to form close packed monolayers.</P><P>These molecules by virtue of their low ionization potentials andhigh electron affinities have very unusual condensed phase propertiessuch as strong near infrared absorptions (NIR). The study of NIR(4,000-10,000 cm-l) absorbing films can be justified by theirimportance to optoelectronic applications of inexpensivesemiconductor lasers. New areas of research include films composed ofinorganic complexes having polyaromatic ligands and poly aromaticheterocycles. Our objective here is to establish the criterianecessary to form new, organized 2-D materials, with the specificemphasis on the role of molecular size and shape on orientation andmolecular packing in 2-dimensions.</P><P>The second method uses electrochemistry to produce polymer films<I>in situ</I>.. The oxidative coupling of aromatic amine monomersleads to polymeric materials that are oxidatively reversible,semiconductive and have intense vibrant color changes. We use thisknowledge to design devices like thin layer batteries, photovoltaics,frequency doublers and electrochromic windows.</P><P>Click here to see an <A HREF="DNTD.html">ELECTROCHROMIC WINDOW</A>based on DNTD polymers</P><P>&nbsp;</P><P>Recent Publications:</P><P>Balasubramanian, K.K.; Cammarata, V. "Langmuir-Schaefer Films ofDistyrylphenanthrolines and Rhenium Tricarbonyl Chloride Complexes:Headgroup Influence on Anisotropy" Langmuir, 1996, 12, 4882.</P><P>Wang, L.; Cammarata, V.; "Electropolymers Based on Diphenylamine:¹-Stacking in Cationic Benzidine Units" Thin Solid Films, 1996,284-285, 297.</P><P>Balasubramanian, K.K.; Cammarata, V.; "Polymerization andCharacterization of Distyryl Bipyridines in Solution andLangmuir-Schaefer Films: Effect of Preorganization" Langmuir, 1996,12, 2035.</P><P>Wang, L.; Goodloe, G.W.; Stallman, B.J.; Cammarata, V.;"Synthesis, Electroxidation and Char-acterization ofBis(diphenylamine)naphthalene Diimide" Chem. Mater., 1996, 8, 1175.</P><P><HR></P><P ALIGN=CENTER>[<B><A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/index.html">CHEMISTRY</A></B>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/degrees.html">DEGREES</A>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/classes.html">CLASSES</A>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/faculty.html">FACULTY</A>]<BR>[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/staff.html">STAFF</A>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/research.html">RESEARCH</A>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/schedule.html">SCHEDULE</A>]-[<A HREF="http://www.auburn.edu/academic/science_math/chemistry/docs/current.html">CURRENT</A>]</P><P><HR></P><P ALIGN=CENTER><FONT SIZE=2>Last Updated: 30 April 1997 --Maintained by Vince Cammarata(</FONT><FONT SIZE=2><A HREF="mailto:cammavi@mail.auburn.edu">cammavi@mail.auburn.edu</A></FONT><FONT SIZE=2>)</FONT></P><P><HR></P></BODY></HTML>