Hi, my name is

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.

JB Carroll profile image

About Me

JB Carroll profile picture
I am a Materials and Processes (M&P) Engineer focused on finishes and corrosion control in aerospace. I have a PhD in chemistry, with a strong interest in applying chemical principles in unique ways to develop solutions for challenging problems. I am currently working as an M&P Engineer at Boeing in Saint Louis. My Areas of Expertise:
  • Material Analysis
  • Light Metal Inorganic Finishes
  • Corrosion Control
  • Sealants
  • Coatings
  • AI in Spec Support

Experience

Lead Finishes Engineer - Boeing
Sep 2023 - present
I am currently working as lead M&P Finishes Engineer on 777X program at Boeing in Saint Louis. I support the program with sealant, coatings, and corrosion control questions, as well as assist in drawing reviews. I also support the vast majority of programs on-site with emergent issues.
Lead Analytical Chemistry Engineer
May 2015 - Sep 2023
I supported all programs at Boeing STL site as well as sites across the enterprise and outside Boeing with analytical chemistry work, leading a lab of 3-5 engineers solving difficult problems for our customers. Expertise with GC/MS, IC, ICP/OES, FTIR (ATR,Microscope), as well as experiment design and data interpretation support.
Oct 2013 - May 2015

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.

  • Developed two standard analytical methods (SAMs) for future analysts.

Education

Doctorate of Chemistry
University of Missouri - Saint Louis
Ph.D. Thesis: Siloles Bearing Coordination-Active 2,5-Substituents: Synthesis, Reactivity, Structural and Spectral Properties.
Bachelor of Science in Chemistry
University of Missouri - Saint Louis
GPA: 3.9 out of 4.0

Graduated Summa Cum Laude with an Honors Certificate from the Pierre Lacled Honors College.

Extracurricular Activities

  • SGA Representative for 2 years
  • Chemistry Club, Pierre Laclede Honors College Student Association

Publications and Patents

Selected works from my research and innovation career.

Peer-Reviewed Papers

Featured Synthesis of 2,5-Substituted Siloles and Optical Study of Interactions with Mercury(II), Copper(II), and Nickel(II) Cations

Authors: James B. Carroll, Janet Wilking

Organometallics 32 (6): 1905-1912 (2013)

DOI: 10.1021/om400022f

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.

Synthesis, Characterization, and Crystal Structures of 1,1-Disubstituted-2,3,4,5-tetraphenylgermoles That Exhibit Aggregation-Induced Emission

Authors: Teresa Bandrowsky, James B. Carroll, Janet Wilking

Organometallics 30 (13): 3559-3569 (2011)

DOI: 10.1021/om200259n

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.

Synthesis and Characterization of 3,6-bis(alkynylaryl)-9,9-diphenyl Substituted Silafluorenes and Germafluorenes

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.

Patents

Featured Cyclic germanium compounds and applications thereof

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.

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