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Alexander M. Spokoyny

California NanoSystems Institute

ORCID: 0000-0002-5683-6240

Publishes on Crystallization and Solubility Studies, X-ray Diffraction in Crystallography, Boron Compounds in Chemistry. 384 papers and 8.9k citations.

384Publications
8.9kTotal Citations

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Top publicationsby citations

Infinite coordination polymer nano- and microparticle structures
Alexander M. Spokoyny, Dong-Woo Kim, Abdelqader Sumrein et al.|Chemical Society Reviews|2009
Cited by 784

Infinite coordination polymer particles (ICPs) represent an area of growing interest in chemistry and materials science due to their unique and highly tailorable properties. These structures can be conveniently synthesized in high yields from the appropriate metal salts and bifunctional ligand precursors. Unlike conventional metal-organic framework materials (MOFs), these ICPs exhibit a higher level of structural tailorability, including size- and morphology-dependent properties, and therefore, the promise of a wider scope of utility. A variety of methods now exist for making numerous compositions, with modest control over particle size and shape. These structures can exhibit microporosity, tunable fluorescence, magnetic susceptibility, and unusual catalytic activity and selectivity. Perhaps most importantly, many of these ICP structures can be depolymerized (sometimes reversibly) much faster and under milder conditions than MOFs, which makes them attractive for a variety of biomedical applications. Thus far, several types of ICPs have been explored as contrast agents for magnetic resonance imaging and drug delivery systems. The groundwork for this emerging field of ICPs has been laid only in the past few years, yet significant advances have already been made. Indeed, this tutorial review introduces the reader to the field of ICPs, providing a guide to the work done so far, with an emphasis on synthesis, applications and future prospects.

A Perfluoroaryl-Cysteine S <sub>N</sub> Ar Chemistry Approach to Unprotected Peptide Stapling
Alexander M. Spokoyny, Yekui Zou, Jingjing Ling et al.|Journal of the American Chemical Society|2013
Cited by 463

We report the discovery of a facile transformation between perfluoroaromatic molecules and a cysteine thiolate, which is arylated at room temperature. This new approach enabled us to selectively modify cysteine residues in unprotected peptides, providing access to variants containing rigid perfluoroaromatic staples. This stapling modification performed on a peptide sequence designed to bind the C-terminal domain of an HIV-1 capsid assembly polyprotein (C-CA) showed enhancement in binding, cell permeability, and proteolytic stability properties, as compared to the unstapled analog. Importantly, chemical stability of the formed staples allowed us to use this motif in the native chemical ligation-mediated synthesis of a small protein affibody that is capable of binding the human epidermal growth factor 2 receptor.