Using first-principles calculations based on density functional theory, we investigated the effects of surface functionalization on the energetic and electronic properties of hydrogenated and chlorinated silicon nanowires oriented along the <112> direction. We show that the band structure is strongly influenced by the diameter of the nanowire, while substantial variations in the formation energy are observed by changing the passivation species. We modeled an octane moiety absorption on the (111) and (110) surface of the silicon nanowire to address the effects on the electronic structure of the chlorinated and hydrogenated systems. We found that the moiety does not substantially affect the electronic properties of the investigated systems. Indeed, the states localized on the molecules are embedded into the valence and conduction bands, with no generation of intragap energy levels and moderated change in the band gap. Therefore, Si-C bonds can enhance protection of the hydrogenated and chlorinated nanowire surfaces against oxidation without substantial modification of the electronic properties. However, we calculated a significant charge transfer from the silicon nanowires to the octane moiety.
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http://dx.doi.org/10.3390/nano12091590 | DOI Listing |
Molecules
November 2024
Center for Computational Quantum Chemistry, University of Georgia, Athens, GA 30602, USA.
Hericene is an unusual hexaolefin consisting of three 1,3-diene units located on a rigid bicyclo [2.2.2]octane framework that restricts the geometrical relationships of metal atoms bonded to these olefinic units.
View Article and Find Full Text PDFMar Drugs
November 2024
Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
A detailed chemical study of the culture of a coral-derived fungus resulted in the isolation and identification of four new aromatic heterocycles chrysoquinazolinones A-B (-) and chrysobenzothiazoles A-B (-), along with a new sorbicillinoid 4-carboxylsorbicillin (). Chrysoquinazolinones A-B (-) combine a quinazolinone fragment with a bicyclo[2.2.
View Article and Find Full Text PDFJ Am Chem Soc
November 2024
Department of Chemistry, Emory University, Atlanta, Georgia 30322, United States.
We report an efficient total synthesis of (±)-phaeocaulisin A, a guaianolide sesquiterpene natural product possessing a complex tetracyclic skeleton embedded with an oxaspirolactone and a fused bicyclic lactone, four oxygen-containing stereocenters, and an 8-oxabicyclo[3.2.1]octane core.
View Article and Find Full Text PDFOrg Biomol Chem
October 2024
School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland, 1010, New Zealand.
Pallamolide A is a 7,8--labdane terpenoid possessing a unique bicyclo[2.2.2]octane core and a spiro-butenolide moiety.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Department of Organic Chemistry, Indian Institute of Science, Bangalore, 560012, India.
Over the past few years, there has been a surge of interest in the chemistry of bicyclobutanes (BCBs). Although BCBs have been used to synthesize bicyclo[2.1.
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