ライフサイエンスコーパス: arsine

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1 throline and L-L is either a phosphine or an arsine.

2 pounds do not form any or only less volatile arsines.

3 ne pressurized under nitrogen and doped with arsine and a propylene real sample from a cracker plant

4 s at 20 degrees C, a loss of only 25-50% for arsine and stibine and the above-mentioned tin compounds

5 reduces the production of the less volatile arsines and iAs is almost exclusively formed, therefore

6 The molecular structures of the arsine, arsenide, and arsinidene complexes are described

7 ) was unambiguously identified together with arsine (AsH(3)) as reaction products.

8 its at ppbv to ppmv levels were obtained for arsine (AsH(3)), phosphine (PH(3)), and hydrogen selenid

9 Fungi produce volatile and toxic arsines, but the physiological roles of arsenic methylat

10 Deprotonation of the yttrium-arsine complex [Cp'3Y{As(H)2Mes}] (1) (Cp'=eta(5)-C5H4Me

11 ries of structurally differentiated cationic arsines containing imidazolium, cyclopropenium, formamid

12 t hydrogen ions concentration leading to the arsine formation from iAs compounds detected as As(III)

13 Arsine generation is the gateway for several sensitive a

14 cation exchange column connected in series)-arsine generation-ICP-MS system provided complete separa

15 An electrochemical arsine generator (EAG) is especially green: we report he

16 of monodentate and bidentate phosphines and arsines have been screened in the coupling of alkyl hali

17 An arsine in nitrogen standard was used for optimization an

18 is reviewed for the on-demand production of arsine in turnkey electrochemical generators.

19 Arsine is absorbed into a potassium permanganate solutio

20 he first report on the use of alpha-cationic arsine ligands in catalysis.

21 alladium-based precatalysts and phosphine or arsine ligands were screened to validate the approach ta

22 ective electrochemical hydride generation of arsine over stibine during the deposition step.

23 -As intramolecular coupling in the phosphine-arsine peri-substituted acenaphthene 3, affording therma

24 arsenic in each subfraction are converted to arsine sequentially by hydride generation at pH 4.50 and

25 iAs forms volatile arsine species with high efficiency when treated with Na

26 ystem with arsenic in situ electroreduced to arsine that is reacted with ozone to emit light.

27 emistry of the newly prepared alpha-cationic arsines toward different metal centers and their reactiv

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