Tammy Munsch


Email: tmunsch@purdue.edu

Office: BRWN B125B            Office Phone:  765-494-7359
Lab: BRWN B125B 
                Lab Phone:  765-494-7359

 

Education:

Ph.D. Student, Purdue University, West Lafayette, IN    2001-Present

B.S. in Chemistry, Kansas State University, Manhattan, KS    2001

 

Awards:

Bilsland Dissertation Fellowship  2005-2006

Herbert C. Brown Organic Research Award    2005

ACS Division of Organic Chemistry Graduate Fellowship    2004-2005

Robert R. Squires Scholar     2003-2004

Kansas State University Basic Cancer Research Award    2000, 2001

NSF-Research Experience for Undergraduates, University of Nebraska-Lincoln    2000

Phi Lambda Upsilon (PLU) Travis Miller Senior Award    2001

PLU Junior Award    2000

 

Current Research

Flowing Afterglow Studies of Triradicals and Nitrene Radicals

 

 

 

 

 

 

 

 


Mass spectrometry can be used to study the structure, energetics, and reactivity of reactive intermediates, such as biradicals and triradicals.  My research has focused on the reactivity and thermochemistry of organic triradicals, as well as reactivity studies of distonic diradical anions using flowing afterglow-triple quadrupole mass spectrometry.  More specifically, I have determined the thermochemical properties of 5-dehydro-1,3-quinodimethane (DMX), 3 an organic triradical with an “open-shell” doublet ground state.  Although low-spin, open-shell states can occur in molecules containing transition metals, the ground states of organic molecules are rarely of this type.  Organic biradicals can have open-shell singlet ground states, depending on the orbital structure, but DMX is the first example of an organic triradical with an open-shell doublet ground state. In addition, I characterized the electronic structure of its corresponding biradical anion (DMX-)2 by using chemical reactivity studies.

Currently, I am investigating the thermochemical properties of the dehydrophenylnitrenes.  Calculations carried out by Bettinger and Sander (JACS, 2003, 125, 9726) predict quartet ground states for the o- and p-dehydrophenylnitrenes, whereas m-dehydrophenylnitrene is predicted to have a doublet ground state.  In this project, we are working to develop an approach to experimentally assess the electronic ground states of these triradicals.

 

 Publications

1)  Munsch, Tamara E.; Wenthold, Paul G.; "Organic Gas-Phase Ion Chemistry" Annu. Rep. Prog. Chem., Sect. B, 2004, 100, 377-405.

2)  Munsch, Tamara E.; Slipchenko, Lyudmila V.; Krylov, Anna I.; Wenthold, Paul G. "Reactivity and Structure of the 5-Dehydro-m-xylylene Anion" J. Org. Chem. 2004, 69,  5735-5741.

3)  Slipchenko, Lyudmila V.; Munsch, Tamara E.; Wenthold, Paul G.; Krylov, Anna I. "5-Dehydro-1,3-quinodimethane: A Hydrocarbon with an Open Shell Doublet State" Angew. Chem. Int. Ed. Eng., 2004, 43, 742-745.

4)  Munsch, Tamara E.; Wenthold, Paul G. "Organic Gas-Phase Ion Chemistry" Annu. Rep. Prog. Chem., Sect. B, 2003, (99), 420-446.

5)  Warmuth, R.; Munsch, T. E.; Stalker, R. A.; Li B.; Beatty, A. "Enantioselective synthesis of benzocyclic a,a-dialkyl-amino acids: new insight into the solvent dependent stereoselectivity of TMSCN addition to phenylglycinol derived imines"  Tetrahedron, 2001, 57, 6383-6397.

6)  Stalker, R. A.; Munsch, T. E.; Tran, J. D.; Nie, X.; Warmuth, R.; Beatty, A.; Aakeröy, C. B.  "Asymmetric Synthesis of two new Conformationally Constrained Lysine Derivatives" Tetrahedron, 2002, 58, 4837-4849.