R
Raphael G. Raptis
Researcher at Florida International University
Publications - 162
Citations - 3769
Raphael G. Raptis is an academic researcher from Florida International University. The author has contributed to research in topics: Crystal structure & Pyrazole. The author has an hindex of 36, co-authored 155 publications receiving 3569 citations. Previous affiliations of Raphael G. Raptis include Nanyang Technological University & Australian National University.
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Journal ArticleDOI
Synthesis and Structural Characterization of Trinuclear CuII−Pyrazolato Complexes Containing μ3-OH, μ3-O, and μ3-Cl Ligands. Magnetic Susceptibility Study of [PPN]2[(μ3-O)Cu3(μ-pz)3Cl3]
Panagiotis A. Angaridis,Peter Baran,R. Boča,Francisco Cervantes-Lee,W. Haase,Gellert Mezei,Raphael G. Raptis,R. Werner +7 more
TL;DR: The nine-membered [−CuII−N−N −N−]3 ring of trimeric copper−pyrazolato complexes provides a sturdy framework on which water is twice deprotonated in consecutive steps, forming μ3-OH and µ3-O species as discussed by the authors.
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Syntheses and x-ray structures of group 11 pyrazole and pyrazolate complexes. X-ray crystal structures of bis(3,5-diphenylpyrazole)copper(II) dibromide, tris(.mu.-3,5-diphenylpyrazolato-N,N')trisilver(I)-2-tetrahydrofuran, tris(.mu.-3,5-diphenylpyrazolato-N,N')trigold(I), and hexakis(.mu.-3,5-diphenylpyrazolato-N,N')hexagold(I)
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Anion Encapsulation by Neutral Supramolecular Assemblies of Cyclic CuII Complexes: A Series of Five Polymerization Isomers, [{cis‐CuII(μ‐OH)(μ‐pz)}n], n=6, 8, 9, 12, and 14
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Structure of tris(.mu.-3,5-diphenylpyrazolato-N,N')tricopper(I). Structural comparisons with the silver(I) and gold(I) pyrazolate trimers
TL;DR: Le compose du titre cristallise dans le systeme triclinique avec le groupe d'espace P1 and sa structure est affinee jusqu'a 0,0636.
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Bielschowskysin, a Gorgonian-Derived Biologically Active Diterpene with an Unprecedented Carbon Skeleton
Jeffrey Marrero,Abimael D. Rodriguez,Peter Baran,Raphael G. Raptis,Juan A. Sánchez,Eduardo Ortega-Barria,Todd L. Capson +6 more
TL;DR: Bielschowskysin was shown to exhibit antimalarial activity against Plasmodium falciparum as well as strong anticancer activity against two human cancer cell lines.