ライフサイエンスコーパス: 1,2-dichloroethane

1 izations of cis-enediynes (see scheme; DCE = 1,2-dichloroethane).

2 de submerged in an organic continuous phase (1,2-dichloroethane).

3 ith BF3.Et2O and excess pyrrole in refluxing 1,2-dichloroethane.

4 basic solvents benzene, dichloromethane, and 1,2-dichloroethane.

5 and singlet oxygen quantum yield obtained in 1,2-dichloroethane.

6 ubmicrometer water nanodroplets suspended in 1,2-dichloroethane.

7 in single aqueous microdroplets suspended in 1,2-dichloroethane.

8 cals and selectively convert chloroethane to 1,2-dichloroethane.

9 ,6-TCP) to 4-CP, and tetrachloroethene (PCE)/1,2-dichloroethane (1,2-DCA) completely to ethene.

10 1,2-Dichloroethane (1,2-DCA) is a chlorinated solvent cl

11 both aerobic and anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) using five microbial cultur

12 tionation during anaerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via dihaloelimination by De

13 actionation during aerobic biodegradation of 1,2-dichloroethane (1,2-DCA) via oxidative cleavage of a

14 ollutants under laboratory conditions, e.g., 1,2-dichloroethane, 1,2,3-trichloropropane and gamma-hex

15 The presence of 1,2-dichloroethane (10mgL(-1)) was proved unambiguously

16 on of other environmental pollutants such as 1,2-dichloroethane (72 years), paraoxon (13 months), atr

17 However, monomerization of CP 3 in dry 1,2-dichloroethane affords bright green diamagnetic Co(I

18 hancements were also obtained in the solvent 1,2-dichloroethane, although the analysis of the system

19 ethyl chloride and hydroxide ion and between 1,2-dichloroethane and acetate in solution.

20 ransfer voltammetry at the interface between 1,2-dichloroethane and an aqueous buffer solution or und

21 We demonstrate the quantification of 1,2-dichloroethane and nitrobenzene into water, yielding

22 conditions induced by osmocene dissolved in 1,2-dichloroethane and the subsequent water splitting by

23 duction of 1,1,2-TCA, which can produce both 1,2-dichloroethane and vinyl chloride, was assessed for

24 that were made for 4-chlorotetrahydropyran, 1,2-dichloroethane, and benzyl alcohol have also confirm

25 tion of water-solvent systems, viz: octanol, 1,2-dichloroethane, and cyclohexane.

26 methylsulfoxide, acetonitrile, nitromethane, 1,2-dichloroethane, and dichloromethane, carried out usi

27 of the DhlA structures using the substrate, 1,2-dichloroethane, and halide ions as probes.

28 n in toluene, THF, tetrahydropyran, i-PrOAc, 1,2-dichloroethane, and MeCN with k(rel) of 7-16.

29 s are uncompetitive inhibitors of XaDHL with 1, 2-dichloroethane as the varied substrate at pH 8.2 (C

30 to inconclusive results in another case with 1,2-dichloroethane as substrate.

31 uCl2(p-cymene)}2], AgSbF6, and (NH4)2S2O8 in 1,2-dichloroethane at 100 degrees C for 24 h to afford o

32 s determined for the duplex trimer by ITC in 1,2-dichloroethane at 20 degrees C.

33 s determined for the duplex trimer by ITC in 1,2-dichloroethane at 20 degrees C.

34 Cl(3) catalyst and the t-BuOOt-Bu oxidant in 1,2-dichloroethane at 70 C, affords 3-alkyl-3-(hydroxyar

35 ydes in the presence of 30 mol % BF3.OEt2 in 1,2-dichloroethane at 80 degrees C affords a novel class

36 lecular aza-6pai-annulation/aromatization in 1,2-dichloroethane at 80 degrees C.

37 omatic pollutants, including vinyl chloride, 1,2-dichloroethane, benzene, and toluene.

38 The S(N)2 displacement of Cl(-) from 1,2-dichloroethane by acetate (CH(3)CO(2)(-)) in water a

39 dentical isotope effects in the reduction of 1,2-dichloroethane by Dehalococcoides and cobalamin (Deh

40 inetic tests revealed that dechlorination of 1,2-dichloroethane by the consortium was strongly inhibi

41 e chemically stable solution of this salt in 1,2-dichloroethane can be used as "diazonium ink".

42 e microclouds with alternating voltage cause 1,2-dichloroethane (ClH(2)C-CH(2)Cl) to be converted to

43 Although both vinyl chloride and 1,2-dichloroethane could be simultaneously transformed t

44 yst for breaking the aliphatic C-Cl bonds in 1,2-dichloroethane (DCA) and trichloroethylene (TCE), ar

45 actor (MBR) was tested for bioremediation of 1,2-dichloroethane (DCA) in groundwater.

46 However, the electrochemical valorization of 1,2-dichloroethane (DCA) is currently challenged by the

47 , has been used to elucidate the reaction of 1, 2-dichloroethane (DCE) with the carboxylate of Asp-12

48 S(N)2 displacement reaction of chloride from 1,2-dichloroethane (DCE) by nucleophilic attack of the c

49 t-Ir wire electrode is placed across a H(2)O/1,2-dichloroethane (DCE) interface, creating a Pt-Ir/H(2

50 phthalenesulfonate (DNNS) at polarized water/1,2-dichloroethane (DCE) interfaces, i.e., sDNNS(-) (DCE

51 ) dissolved in a tetrahydrofuran (THF) and a 1,2-dichloroethane (DCE) solution, respectively, using p

52 erty of dimethyl sulfoxide (DMSO) along with 1,2-dichloroethane (DCE) was exploited for the incorpora

53 r as well as acetonitrile and cyclohexane in 1,2-dichloroethane (DCE).

54 in methanol (MeOH), acetonitrile (ACN), and 1,2-dichloroethane (DCE).

55 a potential window distinct from that of the 1,2-dichloroethane (DCE)/water ITIES.

56 are reported in the current-time response of 1,2-dichloroethane(DCE)|water(W) submilli-interfaces aft

57 nors and 1,2,4,5-tetracyanobenzene (TCNB) in 1,2-dichloroethane (DCLE) exhibit a mirror image relatio

58 In the case of 1,2-dichloroethane dechlorination, a 6-fold improvement

59 ved at the interface for various oil phases (1,2-dichloroethane, dichloromethane, chloroform, and nit

60 transformed to ethene, prolonged exposure to 1,2-dichloroethane diminished the vinyl chloride transfo

61 DBU=1,8-diazabicyclo[5.4.0]undec-7-ene, DCE=1,2-dichloroethane, DMS=dimethylsulfide).

62 hlorethane droplet, CO(2) accumulates in the 1,2-dichloroethane droplet.

63 ly varying polarities: cyclohexane, toluene, 1,2-dichloroethane, ethyl acetate, acetone, acetonitrile

64 ur detectable reductive dehalogenases during 1,2-dichloroethane exposure, suggesting that it catalyze

65 etween two immiscible electrolyte solutions, 1,2-dichloroethane-H2O.

66 Organic haloalkanes, such as 1,2-dichloroethane, have a negligible interfering effect

67 over time, given the relative solubility of 1,2-dichloroethane in the water continuous phase, the ch

68 1) Ru(bpy)(3)(2+) transfer through the water/1,2-dichloroethane interface and (2) electrodeposition o

69 ase and is surprisingly trapped at the water|1,2-dichloroethane interface and continues to grow.

70 odeposition of Pd nanoparticles at the water/1,2-dichloroethane interface.

71 ase in transfer of propranolol at an aqueous-1,2-dichloroethane interface.

72 ArF(-)) salt with phosphine oxides OPR(3) in 1,2-dichloroethane is exothermic and leads to the popula

73 By precisely positioning a 1,2-dichloroethane microdroplet onto the ultramicroelect

74 resence of scandium or ytterbium triflate in 1,2-dichloroethane or a cosolvent mixture of 1/9 THF/dic

75 The transformations were performed in 1,2-dichloroethane or acetonitrile under reflux and gave

76 ost detains three molecules each of CHCl(3), 1,2-dichloroethane, or isopropyl chloride.

77 ansfer reaction (DeltaG('aq->org)) and water-1,2-dichloroethane partition coefficient (logP(DCE)('))

78 ansfer reaction (DeltaG('aq->org)) and water-1,2-dichloroethane partition coefficient (logP(water/DCE

79 ride (PVC) synthesis, yet selectivity toward 1,2-dichloroethane remains challenged by uncontrolled ov

80 A 1,2-dichloroethane solution containing a commercially av

81 ned in good to excellent yield by stirring a 1,2-dichloroethane solution of the starting triazene wit

82 bon monoxide) chloride] ion pairs in MeCN or 1,2-dichloroethane solutions.

83 The cascade reactions proceed in 1,2-dichloroethane solvent under visible-light irradiati

84 In the more polar solvent 1,2-dichloroethane, some salts form both contact and sol

85 nzyme haloalkane dehalogenase (DhlA), with a 1,2-dichloroethane substrate.

86 In 1,2-dichloroethane the solution is heterogeneous, while

87 stereochemical memory effect in toluene and 1,2-dichloroethane, the reactions in these solvents can

88 Cp*=C(5)Me(5), DCE=1,2-dichloroethane, THF=tetrahydrofuran.

89 uch acid-tolerant OHRB, capable of respiring 1,2-dichloroethane to ethene across a broad pH range, wi

90 catalyzes the reductive dihaloelimination of 1,2-dichloroethane to ethene.

91 vironmentally important dihaloelimination of 1,2-dichloroethane to ethene.

92 dictates product distribution shifting from 1,2-dichloroethane to trichloroethane.

93 served that increasing the influent ratio of 1,2-dichloroethane to trichloroethene was associated wit

94 (tetrachloromethane) and on TDIROF for 90% (1,2-dichloroethane) to 100% (trichloromethane) of what w

95 ion of chlorinated organic compounds such as 1,2-dichloroethane, trichloroethylene, and tetrachloroet

96 lytic amount of anhydrous FeCl3 in refluxing 1,2-dichloroethane underwent tandem Conia-ene and Friede

97 ased and subsequent exposure of the films to 1,2-dichloroethane vapor led to a significant increase i

98 hlorination, promote bidentate adsorption of 1,2-dichloroethane via hydrogen-bond networks, thereby a

99 emical extraction of rubidium at micro water|1,2-dichloroethane (w|DCE) and water|room-temperature io

100 of carbon tetrachloride-water (CCl4-H2O) and 1,2-dichloroethane-water (DCE-H2O).

101 The transfer of these analytes across a 1,2-dichloroethane/water interface was studied by cyclic

102 ansfer of tetraethylammonium (TEA(+)) at the 1,2-dichloroethane/water interface.

103 ized poly(vinyl chloride) membrane/water and 1,2-dichloroethane/water interfaces.

104 tions across the interface between water and 1,2-dichloroethane were measured by steady-state voltamm

105 onger chained OCBPs (1,2-dichloropropane and 1,2-dichloroethane) were more frequently found on TDIROF

106 n tobacco resulting in the dehalogenation of 1,2-dichloroethane, which was otherwise recalcitrant.

107 by different isotope effects in reaction of 1,2-dichloroethane with Dehalogenimonas (epsilon(C) = -2