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1 els of arsenate (As(V)) in drinking water as arsine.
2 throline and L-L is either a phosphine or an arsine.
3 he standard reached with tris-trimethylsilyl arsine.
4 pounds do not form any or only less volatile arsines.
5 ne pressurized under nitrogen and doped with arsine and a propylene real sample from a cracker plant
6 ynthesis of InAs NCs with tris(dimethylamino)arsine and alane N,N-dimethylethylamine as the reducing
7 s at 20 degrees C, a loss of only 25-50% for arsine and stibine and the above-mentioned tin compounds
8  reduces the production of the less volatile arsines and iAs is almost exclusively formed, therefore
9 4,6-triiodobenzene with triphenylphosphine, -arsine, and -stibine provides cocrystals based on I...P,
10                                A new triaryl arsine (Ar(3)As)-based metal-organic framework (MOF) nam
11              The molecular structures of the arsine, arsenide, and arsinidene complexes are described
12 ioctylamine coupled with tris(trimethylsilyl)arsine as arsenic precursor and oleic acid as ligand.
13    Here, we present a comprehensive study of arsine (AsH(3) ) on the germanium (001) surface.
14 ) was unambiguously identified together with arsine (AsH(3)) as reaction products.
15 its at ppbv to ppmv levels were obtained for arsine (AsH(3)), phosphine (PH(3)), and hydrogen selenid
16             Fungi produce volatile and toxic arsines, but the physiological roles of arsenic methylat
17                 Deprotonation of the yttrium-arsine complex [Cp'3Y{As(H)2Mes}] (1) (Cp'=eta(5)-C5H4Me
18 ries of structurally differentiated cationic arsines containing imidazolium, cyclopropenium, formamid
19 y and that further understanding of biogenic arsine evolution and degradation are required to adequat
20 t hydrogen ions concentration leading to the arsine formation from iAs compounds detected as As(III)
21                                              Arsine generation is the gateway for several sensitive a
22  cation exchange column connected in series)-arsine generation-ICP-MS system provided complete separa
23                           An electrochemical arsine generator (EAG) is especially green: we report he
24 of germanium with the enhanced properties of arsine/germanium chemistry that promises scale-up to lar
25  of monodentate and bidentate phosphines and arsines have been screened in the coupling of alkyl hali
26 ilable chemicals, such as tris(dimethylamino)arsine, have recently emerged as alternative As precurso
27                                           An arsine in nitrogen standard was used for optimization an
28  is reviewed for the on-demand production of arsine in turnkey electrochemical generators.
29 tes the premise that incorporation of organo(arsines) into MOF scaffolds is a safer and more convenie
30                                              Arsine is absorbed into a potassium permanganate solutio
31 d C5 positions in good yields, enabled by an arsine ligand and a unique amide-based NBE.
32 he first report on the use of alpha-cationic arsine ligands in catalysis.
33 alladium-based precatalysts and phosphine or arsine ligands were screened to validate the approach ta
34 ective electrochemical hydride generation of arsine over stibine during the deposition step.
35                                       Phenyl arsine oxide (PAO) is a vesicant, similar to Lewisite, a
36                      The arsenical trimethyl arsine oxide accounted for the majority of extractable o
37                         Phosphine oxides and arsine oxides are common laboratory reagents with divers
38          In contrast to phosphine oxides and arsine oxides, which are common and exist as stable mono
39 -As intramolecular coupling in the phosphine-arsine peri-substituted acenaphthene 3, affording therma
40 ris-trimethylsilyl (or tris-trimethylgermil) arsine precursors.
41 d a gas-diffusion cell for the separation of arsine prior to its spectrophotometric determination bas
42  ambient temperature seems to cause enhanced arsine release from soils, and potentially also from the
43 arsenic in each subfraction are converted to arsine sequentially by hydride generation at pH 4.50 and
44                           iAs forms volatile arsine species with high efficiency when treated with Na
45 ystem with arsenic in situ electroreduced to arsine that is reacted with ozone to emit light.
46 rsine ((TMSi)(3)As) and tris-trimethylgermyl arsine ((TMGe)(3)As), several attempts have been made to
47 senic precursors such as tris-trimethylsilyl arsine ((TMSi)(3)As) and tris-trimethylgermyl arsine ((T
48 emistry of the newly prepared alpha-cationic arsines toward different metal centers and their reactiv