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Atomic Size Misfit for Electrocatalytic Small Molecule Activation
This review explores the application and mechanisms of atomic size misfit in catalysis for small molecule activation, focusing on how structural defects and electronic properties can effectively lower the energy barriers of chemical bonds in molecules like H2O, CO2, and N2.
Ping Hong +3 more
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Expanding the fluorescence toolkit: molecular design, synthesis and biological application of unnatural amino acids. [PDF]
Marshall O, Sutherland A.
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Characterization of Cyclic [n]Spirobifluorenylene Compounds and Electron Delocalization in Their Radical Cation Species. [PDF]
Imai T, Amaya T.
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Redirecting electron flows in glutamate oxidases by selective anchoring of osmium complexes. [PDF]
Han M +4 more
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Formulation methods for peptide-modified lipid nanoparticles. [PDF]
Miyasaki K +5 more
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β-alkoxy enones for biocompatible primary amine conjugation. [PDF]
Zhang Z +7 more
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Cyclic Conjugated Diacetylenes
Synthetic Communications, 1972Abstract The synthesis of α-bisethynyl compounds, IV and VIII, and cyclic conjugated diacetylenes, V and IX, was performed according to Scheme 1. Bisethynyl compounds, IV and VIII, were prepared in good yields by ethynylation of bromides II, III and VII in N-ethyl-2-pyrrolidone with liquied ammonia solution of sodium acetylide at atmospheric pressure ...
T. Matsuoka, T. Negi, S. Misumi
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Improved cyclic and conjugate cyclic music
Processing Workshop Proceedings, 2004 Sensor Array and Multichannel Signal, 2005By exploiting cyclostationarity that is inherent in many communications signals, cyclic MUSIC has been shown to be able to perform signal selective direction of arrival (DOA) estimation under colored noise and clutter. However, the DOA estimation of cyclic MUSIC is actually biased.
H. Tan, H.H. Fan
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Synthesis of Cyclic Conjugated Polyolefins
Nature, 1947Considerable interest is attached to the properties of cyclic conjugated polyolefins1, and in a number of studies we have been exploring possible routes to analogues and derivatives of such mono- and bi-cyclic structures as those of cyclo-octatetraene and azulene.
D H S, HORN, J R, NUNN, W S, RAPSON
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