A DFT study of the adsorption behavior and sensing properties of CO gas on monolayer MoSe in CO-rich environment.

Context: Carbon monoxide, also known as the "silent killer," is a colorless, odorless, tasteless, and non-irritable gas that, when inhaled, enters the bloodstream and lungs, binds with the hemoglobin, and blocks oxygen from reaching tissues and cells. In this work, the monolayer MoSe-based CO gas sensors were designed using density functional theory calculation with several dopants including Al, Au, Pd, Ni, Cu, and P. Here, Cu and P were found to be the best dopants, with adsorption energies of -0.

Correction: Controlled p-type substitutional doping in large-area monolayer WSe crystals grown by chemical vapor deposition.

Correction for 'Controlled p-type substitutional doping in large-area monolayer WSe2 crystals grown by chemical vapor deposition' by Stephen A. Campbell et al., Nanoscale, 2018, 10, 21374-21385.

Controlled p-type substitutional doping in large-area monolayer WSe crystals grown by chemical vapor deposition.

Tungsten diselenide (WSe) is a particularly interesting 2D material due to its p-type conductivity. Here we report a systematic single-step process to optimize crystal size by variation of multiple growth parameters resulting in hexagonal single crystals up to 165 μm wide. We then show that these large single crystals can be controllably in situ doped with the acceptor Niobium (Nb).

Anorectal Malformation: Paediatric Problem Presenting in Adult.

This is a case report of 22-year-old girl admitted with abdominal distension, vomiting, and chronic constipation since birth. Abdomen was distended, and perineal examination revealed imperforate anus with vestibular fistula (ARM). So far worldwide very few cases have been reported about anorectal malformation presenting in adulthood, and thus extremely little data is available in the literature about an ideal management of anorectal malformation in adults.

Dialkyltin(IV)bis(O-tolyl/benzyldithiocarbonate) complexes: spectroscopic, thermogravemetric, antifungal and crystal analysis of n-Bu2Sn(S2COCH2C6H5)2.

Novel compounds of dimethyl- and dibutyltin(IV) with O-tolyl/benzyldithiocarbonates were successfully obtained by the reaction of Me(2)SnC(l2) and n-Bu(2)SnCl(2) with sodium salt of O-tolyl/benzyldithiocarbonates, [o-, m- and p-CH(3)C(6)H(4)OCS(2)Na and C(6)H(5)CH(2)OCS(2)Na], in 1:2 molar ratio in dry toluene. The structure of these newly synthesized complexes has been examined by elemental analysis, FT-IR, multinuclear NMR ((1)H, (13)C and (119)Sn) spectroscopy. The thermal behaviour of the complex (8) has been studied by TGA/DTA analysis.

Blue electroluminescence from Sb-ZnO/Cd-ZnO/Ga-ZnO heterojunction diode fabricated by dual ion beam sputtering.

p-type Sb-doped ZnO/i-CdZnO/n-type Ga-doped ZnO was grown by dual ion beam sputtering deposition system. Current-voltage characteristics of the heterojunction showed a diode-like rectifying behavior with a turn-on voltage of ~5 V. The diode yielded blue electroluminescence emissions at around 446 nm in forward biased condition at room temperature.

Synthesis, gene silencing, and molecular modeling studies of 4'-C-aminomethyl-2'-O-methyl modified small interfering RNAs.

The linear syntheses of 4'-C-aminomethyl-2'-O-methyl uridine and cytidine nucleoside phosphoramidites were achieved using glucose as the starting material. The modified RNA building blocks were incorporated into small interfering RNAs (siRNAs) by employing solid phase RNA synthesis. Thermal melting studies showed that the modified siRNA duplexes exhibited slightly lower T(m) (∼1 °C/modification) compared to the unmodified duplex.

The first asymmetric organolithium tetramers with simple ether donor bases.

The donor-free trimethylsilylmethyllithium [LiCH(2)SiMe(3)](6) hexameric aggregate is for the first time broken up by simple ether donors such as diethyl ether (Et(2)O) and tert-butylmethyl ether ((t)BuOMe) to give the unprecedented asymmetric tetramers while the chelating dimethoxyethane (DME) gives the expected dimer.

New chelating ligands based on S-organosulfurdiimides: synthesis and single crystal X-ray structures of their lithium complexes.

Three new diimidosulfinates, [TMSCH(2)S(N(t)Bu)(2)Li](2) (1), [2-PyCH(2)S(N(t)Bu)(2)Li](2) (2), and [{PhCH(2)S(N(t)Bu)(2)Li}(2) x THF] (3) (TMS = trimethylsilyl; Py = 2-pyridyl), have been synthesized by the reaction of functionalized alpha-CH(2)-organolithium compounds with bis-tert-butylsulfurdiimide. These new organolithium chelates are characterized by NMR ((1)H, (13)C, (7)Li, and (29)Si) spectroscopy and single-crystal X-ray diffraction analyses. Compounds 1 and 2 crystallize as dimers without donor molecules, whereas one of the lithium atoms in 3 is coordinated by a single THF molecule.