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Dive into the research topics where T. Spencer Bailey is active.

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Featured researches published by T. Spencer Bailey.


Journal of the American Chemical Society | 2014

Understanding Hydrogen Sulfide Storage: Probing Conditions for Sulfide Release from Hydrodisulfides

T. Spencer Bailey; Lev N. Zakharov; Michael D. Pluth

Hydrogen sulfide (H2S) is an important biological signaling agent that exerts action on numerous (patho)physiological processes. Once generated, H2S can be oxidized to generate reductant-labile sulfane sulfur pools, which include hydrodisulfides/persulfides. Despite the importance of hydrodisulfides in H2S storage and signaling, little is known about the physical properties or chemical reactivity of these compounds. We report here the synthesis, isolation, and characterization (NMR, IR, Raman, HRMS, X-ray) of a small-molecule hydrodisulfide and highlight its reactivity with reductants, nucleophiles, electrophiles, acids, and bases. Our experimental results establish that hydrodisulfides release H2S upon reduction and that deprotonation results in disproportionation to the parent thiol and S0, thus providing a mechanism for transsulfuration in the sulfane sulfur pool.


Free Radical Biology and Medicine | 2015

Reactions of isolated persulfides provide insights into the interplay between H2S and persulfide reactivity

T. Spencer Bailey; Michael D. Pluth

Hydrogen sulfide is ubiquitous in biological systems and exerts function over a wide range of important physiological processes. Complementing free H2S, the reductant-labile sulfur pool plays significant roles in the translocation and action of sulfide, however the chemistry of reductant-labile sulfide sources has not been studied systematically. Using a combination of NMR and UV-Vis spectroscopy, we investigated the spectroscopic properties and reactivity of three isolated organic persulfides and report a simple model for persulfide reactivity, including their roles as nucleophiles, electrophiles, and sulfide donors.


Methods in Enzymology | 2015

Chemiluminescent Detection of Enzymatically Produced H2S

T. Spencer Bailey; Michael D. Pluth

Hydrogen sulfide (H2S) has emerged as an important biological signaling molecule. To better understand the multifaceted biological roles of H2S, the development of selective and sensitive biocompatible assays for H2S is becoming increasingly important. Motivated by these challenges, our laboratory is developing new methods to further detect and monitor biological H2S. Here, we describe in detail our recent advances in the development and the use of chemiluminescence-based H2S sensors to assist other investigators with use of these chemical tools. We highlight the use of these tools use by displaying their selectivity and high sensitivity toward H2S and provide examples of assays we have developed to detect enzymatically produced H2S.


Journal of the American Chemical Society | 2013

Chemiluminescent Detection of Enzymatically Produced Hydrogen Sulfide: Substrate Hydrogen Bonding Influences Selectivity for H2S over Biological Thiols

T. Spencer Bailey; Michael D. Pluth


Synlett | 2015

Natural Products Containing Hydrogen Sulfide Releasing Moieties

Michael D. Pluth; T. Spencer Bailey; Matthew D. Hammers; Matthew D. Hartle; Hillary A. Henthorn; Andrea K. Steiger


Inorganic Chemistry | 2016

The Intersection of NO and H2S: Persulfides Generate NO from Nitrite through Polysulfide Formation

T. Spencer Bailey; Hillary A. Henthorn; Michael D. Pluth


Chemical Communications | 2015

A simple bioluminescent method for measuring D-amino acid oxidase activity

T. Spencer Bailey; Micah T. Donor; Sean P. Naughton; Michael D. Pluth


Archive | 2013

Chemical Tools for Studying Biological Hydrogen Sulfide

Michael D. Pluth; T. Spencer Bailey; Matthew D. Hammers; Leticia A. Montoya


Archive | 2014

Compounds for determining the presence of hydrogen sulfide and methods of use

Michael D. Pluth; T. Spencer Bailey; Leticia A. Montoya; Taylor F. Pearce


Nitric Oxide | 2014

S9-7 Isolation, characterization, and reactivity of biomimetic hydrodisulfide (RSSH) complexes

Michael D. Pluth; T. Spencer Bailey

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