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1 f 3 with HCl or by direct photolysis of 2 in chlorobenzene.
2 thanogenic culture would completely detoxify chlorobenzene.
3 ulation of benzene, which is more toxic than chlorobenzene.
4 constants were similar in toluene, THF, and chlorobenzene.
5 C=C(t)Bu))(2)][B(C(6)F(5))(4)](2).5PhCl from chlorobenzene.
6 N-bromosuccinimide) and 5 mol % Pd(OAc)2 in chlorobenzene (0.10 molar) at 110 degrees C, pyridine-di
7 for aniline, phenol, benzene, bromobenzene, chlorobenzene, 1,2-dichlorobenzene, 2,4,6-trichloropheno
8 nt sources of chlorobenzene and a mixture of chlorobenzene, 1,2-dichlorobenzene, and 1,4-dichlorobenz
10 : no guest, 611; toluene, 565; benzene, 586; chlorobenzene, 592; p-xylene, 585; mesitylene, 565; etha
11 ; and incubation of cells with 2,4-dinitro-1-chlorobenzene (an inhibitor of thioredoxin reductase) de
12 s, with a kinh of 6.1 x 10(4) M(-1) s(-1) in chlorobenzene and 6.0 x 10(3) M(-1) s(-1) in acetonitril
13 y column studies with contaminant sources of chlorobenzene and a mixture of chlorobenzene, 1,2-dichlo
16 er solid-liquid phase-transfer conditions in chlorobenzene and in the presence of K(3)PO(4) as weak b
17 13)C measure of salmon density, but mercury, chlorobenzenes, and polychlorinated biphenyls (PCBs) wer
18 s were obtained with analytes as volatile as chlorobenzene (approximately 90%) in 1 mL of solvent.
21 4), CHCl(3), CH(2)Cl(2), dichloroethane, and chlorobenzene at -23 degrees C showed little variance.
22 pronounced solvent effect is observed: While chlorobenzene causes the T2 planes to align preferential
23 ies showed that a small percentage of ODT in chlorobenzene (CB) induced the nucleation of polymeric c
24 sites contaminated with nitrobenzene (NB) or chlorobenzene (CB) were tested for their biodegradation
25 the vadose zone of a site contaminated with chlorobenzene (CB), 1,2-dichlorobenzene (12DCB), and 1,4
26 of PTB7 film formation from chloroform (CF), chlorobenzene (CB), and 1,2-dichlorobenzene (DCB) soluti
27 ltrichloroethane and its metabolites (DDTs), chlorobenzenes (CBzs)--pentachlorobenzene and hexachloro
28 to evaluate an online monitoring system for chlorobenzene congeners as indicators of polychlorinated
31 p-xylene and the incoming arene is C(6)D(6), chlorobenzene-d(5), anisole-d(8), fluorobenzene-d(5), to
32 rocarbons (mixture of chlorobenzene-h(5) and chlorobenzene-d(5), mixture of 1,2-dichlorobenzene-h(4)
34 d show that benzene derived electrons fueled chlorobenzene dechlorination removing the need to provid
35 of certain HiPco SWNTs upon reaction with 4-chlorobenzene diazonium and 4-hydroxybenzene diazonium s
36 toluminescence (PL) during a reaction with 4-chlorobenzene diazonium in aqueous solution, evidence fo
37 including aromatic hydrocarbons (mixture of chlorobenzene-h(5) and chlorobenzene-d(5), mixture of 1,
39 inated the overall partitioning of the three chlorobenzenes in the 1.5 mum filtrate, and the partitio
40 rmediate biodegradation products benzene and chlorobenzene increased and achieved steady state values
43 and honokiol trapped two peroxyl radicals in chlorobenzene (kinh = 3.8 x 10(4) M(-1) s(-1)) and four
44 d catalytic amounts of pyridine in refluxing chlorobenzene leads to the formation of acyl chlorides.
46 iate chlorine atoms from individual oriented chlorobenzene molecules adsorbed on a Si(111)-7 x 7 surf
47 he use of silver, previously unexplored, and chlorobenzene-normally regarded as relatively inert in s
49 is shows that p-SIDT(FBTTh2)2 spin-cast from chlorobenzene organizes into crystalline domains with la
50 her industrial or byproduct organochlorines (chlorobenzenes, pentachloroanisole, octachlorostyrene),
53 tical lamotrigine and the industrial solvent chlorobenzene, signifying that electrocatalytic treatmen
54 romonomers 16 in the presence of end-capping chlorobenzene solvent to produce the statistical spacerl
55 Enumeration of bacteria capable of degrading chlorobenzenes suggested that most of the biodegradation
56 lion (3-[2,4 dihydroxyphenylazo]-2-hydroxy-5-chlorobenzene sulfonic acid), the DNA stain 4',6-diamino
57 ylbenzene, carbon tetrachloride, chloroform, chlorobenzene, tetrachlorethane, and dichlorobenzene.
58 lture capable of reductive dechlorination of chlorobenzene to benzene with a second benzene-degrading
59 ing from simple aromatics (e.g., aniline and chlorobenzene) to the much larger squalene (M(w) = 411)
60 efficiently than alpha-tocopherol in a water/chlorobenzene two-phase system containing N-acetylcystei
61 ombination resulted in the transformation of chlorobenzene via benzene to the nontoxic degradation pr
65 ch 1,2-dithienyl-1,2-dicyanoethene (4TCE) in chlorobenzene with ultrafast transient absorption spectr
66 alogenation capability of each strain to use chlorobenzenes with three or more chlorines, tetrachloro
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