Many tryptamine derivatives are known to induce altered states of consciousness and are increasingly of interest in forensic and neurobiological studies. The analytical chemistry of certain synthetic routes to the tryptamines is discussed and likely side products and impurities identified, where literature reports are available. Recent examples from the authors' laboratory are presented to highlight future prospects and implications for analytical procedures. The aim of this review is to provide the analytical chemist with the foundation chemistry and some analytical targets to be able to undertake direct characterisation of products and intermediates. These might become available from interdiction of clandestine operations in a forensic environment or during the synthesis of the tryptamines for investigative neurobiological and clinical procedures.
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http://dx.doi.org/10.1016/j.jpba.2004.08.022 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, South Korea.
Epoxides are versatile chemical intermediates that are used in the manufacture of diversified industrial products. For decades, thermochemical conversion has long been employed as the primary synthetic route. However, it has several drawbacks, such as harsh and explosive operating conditions, as well as a significant greenhouse gas emissions problem.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
International Scientific and Technological Cooperation Base of Industrial Solid Waste Cyclic Utilization and Advanced Materials, School of Materials Science and Engineering, North Minzu University, Yinchuan 750021, China.
Sulfur dioxide (SO), a pervasive air pollutant, poses significant environmental and health risks, necessitating advanced materials for its efficient capture. Nanoporous organic polymers (NOPs) have emerged as promising candidates; however, their development is often hindered by high synthesis temperatures, complex precursors, and limited SO selectivity. Herein, we report a room-temperature, cost-effective synthesis of carbazole-based nanoporous organic polymers (CNOPs) using 1,3,5-trioxane and paraldehyde, offering a significant advancement over traditional Friedel-Crafts alkylation methods.
View Article and Find Full Text PDFChemistryOpen
January 2025
Department of Materials Science, Solar Energy Research Center MIB-SOLAR and INSTM Milano-Bicocca Research Unit University of Milano-Bicocca,Via Cozzi 55, Milano, I-20125, Italy.
The rapid proliferation of internet-connected devices has transformed our daily habits prompting a shift towards greater sustainability in renewable energy for indoor applications. Among the various technologies available for obtaining energy in indoor conditions, Dye-Sensitized Solar Cells (DSSCs) stand out as the most promising due to their ability to efficiently convert ambient light into usable electricity. This study explores how the optimal matching of the UV-Vis absorption spectra of dyes commonly used in DSSCs with the emission profiles of indoor lamps allows for the enhanced efficiency of DSSC under indoor lighting.
View Article and Find Full Text PDFWe analyze the single-photon band structure and the transport of a single photon in a one-dimensional coupled-spinning-resonator chain. The time-reversal symmetry of the resonators chain is broken by the spinning of the resonators, instead of external or synthetic magnetic field. Two nonreciprocal single-photon band gaps can be obtained in the coupled-spinning-resonator chain, whose width depends on the angular velocity of the spinning resonator.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
EaStCHEM School of Chemistry, University of St Andrews, North Haugh, St Andrews KY16 9ST, U.K.
New approaches to achieve facile and reversible dihydrogen activation are of importance for synthesis, catalysis, and hydrogen storage. Here we show that low-coordinate magnesium oxide complexes [{(nacnac)Mg}(μ-O)] , with nacnac = HC(RCNDip), Dip = 2,6-PrCH, R = Me (), Et (), Pr (), readily react with dihydrogen under mild conditions to afford mixed hydride-hydroxide complexes [{(nacnac)Mg}(μ-H)(μ-OH)] . Dehydrogenation of complexes is strongly dependent on remote ligand substitution and can be achieved by simple vacuum-degassing of (R = Pr) to regain .
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