JB Carroll.
I use chemistry to support aerospace
Lead Finishes Engineer and Former Lead Analytical Engineer. Using chemistry to solve problems and develop solutions for aerospace.
Lead Finishes Engineer and Former Lead Analytical Engineer. Using chemistry to solve problems and develop solutions for aerospace.


Worked as a scientist supporting primarily LC/MS method development and also other chromatography for non-routine, challenging matrices and analytes. Typical tasks include method development, reverse-engineering, quantification, etc. across consumer products, pharmaceuticals, and food, amongst other industries. Additionally worked with FTIR, ICP/OES, NMR, SEM, and wet chemical methods.
Graduated Summa Cum Laude with an Honors Certificate from the Pierre Lacled Honors College.
Extracurricular Activities
Authors: James B. Carroll, Janet Wilking
Organometallics 32 (6): 1905-1912 (2013)
Several 2,5-diaryl-1,1-dimethyl-3,4-diphenylsiloles (with aryl = p-cyanophenyl (1), m,p-bis(methylthio)phenyl (2), p-N,N-dimethylaminophenyl (3), 2,2′-bipyridin-6-yl (4)) were synthesized and characterized by UV–vis, fluorescence, and NMR spectroscopy, along with crystal structure determinations for 1 and 2. Compounds 1–4 in methylene chloride were combined with 1–10 equiv of M(ClO4)2 (M = Ni, Cu, Hg) in methanol, and the resulting solutions were monitored by UV–vis and fluorescence spectroscopy.
Authors: Teresa Bandrowsky, James B. Carroll, Janet Wilking
Organometallics 30 (13): 3559-3569 (2011)
A series of 2,3,4,5-tetraphenylgermoles with different 1,1-substituents have been prepared, and their UV–vis absorption and fluorescence spectral profiles in solution were determined. A thin-layer chromatography based method was used to measure their solid-state luminescence.
Authors: Stephan Germann, Nigam P. Rath, Teresa Bandrowsky, James B Carroll, Janet Wilking, et. al
Journal of Organometallic Chemistry 1041 : 123849 (2025)
DOI: 10.1016/j.jorganchem.2025.123849
A series of luminescent 3,6-disubstituted-alkynyl(aryl)-9,9-diphenylsilafluorenes and -germafluorenes have been synthesized from the lithium-halogen exchange reaction of 5,5’-dibromo-2,2’-diodo-1,1’-biphenyl followed by a ring closure reaction with Ph2ECl2 (E =Si, Ge). A subsequent Pd-catalyzed Sonogashira coupling reaction with a terminal p-substituted(aryl)alkyne afforded the 3,6-bis(alkynyl)aryl-9,9-diphenylsila- and germafluorenes.
US12441749B2
Inventors: Janet Braddock-Wilking, Teresa Lynn Bandrowsky, James Bryan Carroll
Assignee: University of Missouri St. Louis
Date Issued: May 03, 2022
The present disclosure provides a new series of compounds exhibiting high fluorescence quantum yields in the solid state.