ライフサイエンスコーパス: nitroaromatic

1 sly for the rapid detection of TNT and other nitroaromatics.

2 hich favors the formation of light-absorbing nitroaromatics.

3 losives as well as nitramines, nitrates, and nitroaromatics.

4 ave been designed for selective detection of nitroaromatics.

5 ble of selectively detecting a wide range of nitroaromatics; a possible application in environmental

6 velength shifts in real time, in response to nitroaromatic adsorption, results in the first single-na

7 ted unique fingerprints for each of the nine nitroaromatic analytes tested, including unique response

8 y the sensing mechanisms's ability to detect nitroaromatic analytes, the fluorescent-labeled MIP part

9 The simultaneous measurement of nitroaromatic and ionic explosives is used for demonstra

10 as a postcolumn reagent for the detection of nitroaromatic and nitramine explosive compounds.

11 f a microchip, enabled the separation of six nitroaromatic and nitramine explosives and their degrada

12 per mille), and delta(2)H (<=5 per mille for nitroaromatics and <=10 per mille for aminoaromatics).

13 xplosive molecules including nitrate esters, nitroaromatics and cyclic triazine compounds.

14 We envisage applications to detecting other nitroaromatics and security-related gas targets, and hig

15 te hypothesis for the mechanism of action of nitroaromatic anti-TB agents, in that the cysteine thiol

16 nown nitrovasodilators, but also occurs with nitroaromatic antimicrobials.

17 Nitroaromatics are among the most important and commonly

18 As contaminant nitroaromatics are transported up the roots and stem int

19 lly act as luminescent reporters of volatile nitroaromatics at sub-parts per million levels.

20 ens could indirectly reduce a broad array of nitroaromatics by first respiring NOM components or the

21 at black carbon-mediated reduction of sorbed nitroaromatics by sulfides involves electron transfer di

22 ation combined with the abiotic reduction of nitroaromatics by the hydroquinones formed.

23 ally used for photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,

24 Since many nitroaromatic caged compounds are two-photon active at 7

25 e hydrogenation of alkynes, hydrogenation of nitroaromatics, CO(2) hydrogenation, C-C coupling, and m

26 Here, we used a nitroaromatic compound (NAC) as a reactive probe molecul

27 Monooxygenation is an important route of nitroaromatic compound (NAC) biodegradation and it is wi

28 rrays to monitor fluorescence changes during nitroaromatic compound (NAC) vapor exposure.

29 exposure of the modified QCM surface to the nitroaromatic compound 2,4-dinitrotoluene (DNT) in solut

30 vities of these materials are performed with nitroaromatic compound 4-nitroaniline and the results ar

31 at the modified electrode, depending on the nitroaromatic compound present.

32 ent arrays permit the detection of low-level nitroaromatic compound vapors because of sensor-to-senso

33 of p-nitrophenol, chosen as a representative nitroaromatic compound.

34 mparisons of measurements taken with related nitroaromatic compounds (1,3,5 trinitrobenzene, 1,3 dini

35 observed during the event were attributed to nitroaromatic compounds (NAC), comprising 28 elemental f

36 c analysis of stable C, N, and H isotopes in nitroaromatic compounds (NACs) and characterized biodegr

37 3 by forming secondary chromophores, such as nitroaromatic compounds (NACs) and organonitrates.

38 Nitroaromatic compounds (NACs) are a class of prevalent

39 Nitroaromatic compounds (NACs) are ubiquitous environmen

40 The evaluation of new energetic nitroaromatic compounds (NACs) for use in green munition

41 are fruitfully employed for rapid sensing of nitroaromatic compounds (NACs) where picric acid (PA, as

42 his receptor (and other related pyrenes) and nitroaromatic compounds (NACs), in both solution and in

43 was used in the electrochemical detection of nitroaromatic compounds (NACs).

44 tly scrutinized for the sensing of explosive nitroaromatic compounds (NACs).

45 such as the alkaline hydrolysis of energetic nitroaromatic compounds (NACs).

46 ically investigated the dioxygenation of two nitroaromatic compounds (nitrobenzene and 2-nitrotoluene

47 le aromatic compounds, including an array of nitroaromatic compounds (nitrobenzene, 2-, 3-, and 4-nit

48 etry (PM) determination of several explosive nitroaromatic compounds (NTs) including 2,4,6-trinitroph

49 use toward the electrochemical detection of nitroaromatic compounds 2,4,6-trinitrotoluene (TNT), 2,4

50 articles was investigated by using different nitroaromatic compounds [m-nitroaniline and p-nitroanili

51 nd collisional processes of diazines towards nitroaromatic compounds and also the diazine-modified el

52 Biodegradation pathways of synthetic nitroaromatic compounds and anilines are well documented

53 roup of enzymes that reduce a broad range of nitroaromatic compounds and has potential uses in chemot

54 reductant for the abiotic transformation of nitroaromatic compounds and munition constituents (NACs/

55 zes the reduction of the nitrogroup (NO2) in nitroaromatic compounds and the flavohemoglobin HmpA, wh

56 As previously observed for nitroaromatic compounds and uranium, magnetite stoichiom

57 The nitroaromatic compounds appear to be the actual effector

58 Nitroaromatic compounds are found in brown carbon aeroso

59 Nitroaromatic compounds are groundwater pollutants that

60 Nitroaromatic compounds are major constituents of the br

61 Nitroaromatic compounds are pollutants emitted from biom

62 nitrotoluene degradation genes not only when nitroaromatic compounds are present, but also in the pre

63 tuted aromatic carbons of BTZ043 and related nitroaromatic compounds are the most electron-deficient

64 e activation of evofosfamide and the related nitroaromatic compounds EF5 and FSL-61 was investigated

65 ntaminants, such as chromium or arsenic, and nitroaromatic compounds functioning both as sorbent and

66 While nitroaromatic compounds have been identified as strong c

67 Direct detection of several nitroaromatic compounds in a complex mixture without pri

68 The determination of nitroaromatic compounds in aqueous solution was investig

69 method was also used to separate and detect nitroaromatic compounds in extracts from spiked soil sam

70 riminate between the presence and absence of nitroaromatic compounds in high background vapor mixture

71 cate that the system is capable of detecting nitroaromatic compounds in solution with high sensitivit

72 ligand, implying that nitro group removal of nitroaromatic compounds may be especially important for

73 strates the ability to separate a variety of nitroaromatic compounds of explosive significance in 20

74 Nitroaromatic compounds pose severe threats to public he

75 that the modified electrode detects several nitroaromatic compounds such as nitrophenols, mononitroa

76 xperimental observations help to explain why nitroaromatic compounds such as p-nitrophenol resist pho

77 hemical studies on BTZ043 and the additional nitroaromatic compounds synthesized by us and others con

78 ures dominated the screening hits, including nitroaromatic compounds that induce substrate-like shift

79 f the PEA catabolic pathway is to metabolize nitroaromatic compounds that may accumulate in cells exp

80 ve enzymatic reduction of nitroaliphatic and nitroaromatic compounds to aliphatic amines and amino-,

81 nvestigated the dioxygenation of a series of nitroaromatic compounds to the corresponding catechols b

82 ction of carboxylic acid-decorated TPAs with nitroaromatic compounds was photophysically explored usi

83 JS42 and JS765, allowing for recognition of nitroaromatic compounds while retaining the ability to r

84 The results show that all the nitroaromatic compounds, 2-nitroaniline, 3-nitroaniline,

85 of secondary metabolites, the degradation of nitroaromatic compounds, activation of nitroimidazofuran

86 Nitroaromatic compounds, including 1,3-benzothiazin-4-on

87 eractions with electron-deficient molecules (nitroaromatic compounds, NACs), displaying superior dete

88 e reductive transformation of chlorinated or nitroaromatic compounds, no work exists examining the in

89 cubation in a solution with different single nitroaromatic compounds, reduction peaks in the range fr

90 sensitive chemosensors for the detection of nitroaromatic compounds, such as 2,4,6-trinitrotoluene (

91 ant strategy for bacterial detoxification of nitroaromatic compounds, such as the conversion of 4-nit

92 227 and 232 were key for the recognition of nitroaromatic compounds, while the amino acid at positio

93 tection of 2,4,6-trinitrotoluene and related nitroaromatic compounds.

94 . strain U2 has not been reported to oxidize nitroaromatic compounds.

95 diation strategies directed at TNT and other nitroaromatic compounds.

96 del for the photochemical behavior of larger nitroaromatic compounds.

97 h the NOx/VOCs ratio due to the formation of nitroaromatic compounds.

98 ensors of electron-deficient species such as nitroaromatic compounds.

99 novel quinolones were explored to recognize nitroaromatic compounds.

100 sensitive toward the detection of all three nitroaromatic compounds.

101 lly reduced by the presence of TNT and other nitroaromatic compounds.

102 fides over a 3-day time scale was limited to nitroaromatic compounds.

103 chosen to reassess the therapeutic value of nitroaromatic compounds.

104 anti-TB agents inspired from BTZs and other nitroaromatic compounds.

105 somers in a solution containing a mixture of nitroaromatic compounds.

106 eactions in the alkaline hydrolysis of three nitroaromatic compounds: 2,4,6-trinitrotoluene (TNT), 2,

107 First, we established nitroaromatic concentration ranges that were nontoxic to

108 tive munitions compounds (IMCs) are emerging nitroaromatic contaminants developed by the military as

109 Our study illustrates that dioxygenation of nitroaromatic contaminants exhibits a large C isotope fr

110 This molecule comprises a nitroaromatic core that can be selectively reduced ("unc

111 , classified into lignin pyrolysis products, nitroaromatics, coumarins, stilbenes, and flavonoids.

112 mily that commonly convert anilines to their nitroaromatic counterparts.

113 d microbial NOM respiration sustained by the nitroaromatic-dependent cycling of quinones.

114 developed by conjugating ABA with different nitroaromatic derivatives, which render ABA inactive unt

115 n additional exciton quenching-based optical nitroaromatic detection method, illustrate that function

116 al when bound to one of the newly identified nitroaromatic drugs.

117 Highly absorbing nitroaromatics (e.g., C(6)H(5)NO(4), C(7)H(7)NO(4), C(7)

118 Detection of nitroaromatics employing greener techniques has been one

119 lar triads composed of ferrocene, C(60), and nitroaromatic entities are reported.

120 te (SDS), is used for separating the neutral nitroaromatic explosive and nerve agent compounds, an op

121 The thermal decomposition of a model nitroaromatic explosive, 2,4,6-trinitrotoluene (TNT), is

122 asurement of 2,4,6-Trinitrotoluen (TNT) as a nitroaromatic explosive.

123 Individual nitroaromatic explosives (such as 2,4,6-trinitrotoluene)

124 ctive sensor for the direct determination of nitroaromatic explosives and byproducts is shown based o

125 ing was synthesized for the determination of nitroaromatic explosives and explosive taggants at trace

126 er the same testing conditions, other common nitroaromatic explosives and oxidizing reagents did not

127 In addition, nitroaromatic explosives are found to have unique intera

128 ion of organic nitramine, nitrate ester, and nitroaromatic explosives as well as black powder and bla

129 n energy in condensed phase decomposition of nitroaromatic explosives has been an unresolved issue fo

130 Assessing the fate of nitroaromatic explosives in the subsurface is challengin

131 Additional selectivity of amine-substituted nitroaromatic explosives is achieved by using a photoche

132 n developed and deployed for the analysis of nitroaromatic explosives on surfaces in open air, offeri

133 formation of a colored Janowsky complex with nitroaromatic explosives through reaction of the enolate

134 eloped coating for the selective sampling of nitroaromatic explosives were proved achieving LOD value

135 dly enhanced performance in the detection of nitroaromatic explosives, most probably as a result of t

136 aks for several groups of important anaytes (nitroaromatic explosives, organophosphate nerve agents,

137 r TNT) than Ru=APy in the detection of these nitroaromatic explosives, which was ascribed to the exte

138 hat enables degradation of nitrate ester and nitroaromatic explosives.

139 transition temperatures (T(g)) for detecting nitroaromatic explosives.

140 The catalyst reduced nitroaromatic groups by a six-electron process with a hi

141 or liquid-phase hydrogenation of substituted nitroaromatics (>99 %) and gas-phase hydrogenation of CO

142 aryl chlorides, triflates, and nonaflates to nitroaromatics has been developed.

143 nes and aminoazo dyes, three mycotoxins, two nitroaromatic hydrocarbons, N-nitrosodimethylamine, viny

144 ernative to current fossil-based routes like nitroaromatic hydrogenation, but is challenging because

145 For di-nitroaromatics hydrogenation, it is a challenge to achie

146 bic, such as PAHs, or water soluble, such as nitroaromatics, imidazoles, and other conjugated oxygen-

147 Key BrC chromophores include nitroaromatics, imidazoles, N-heterocycles, polyaromatic

148 dies support the involvement of photoexcited nitroaromatics in consecutive hydrogen and oxygen atom t

149 nsitive for the detection of trace amount of nitroaromatics in solution, solid, and contact mode.

150 8 and 9 also showed enhanced sensitivity for nitroaromatics in the solid state, and their enhanced se

151 ex capable of selectively and fully reducing nitroaromatics into anilines in a biocompatible buffered

152 mers, the different binding strengths of the nitroaromatic isomer guests to the beta-CD host, and exc

153 fferent reduction potentials for the various nitroaromatic isomers, the different binding strengths o

154 Structural data also reveal that nitroaromatic ligands "moonlight" as substrates by displ

155 an be quenched by numerous agents, including nitroaromatics like TNT and nitramines like RDX, it is d

156 r the detection of 2,4,6-trinitrotoluene via nitroaromatic markers is shown.

157 Nitrobenzene is the smallest nitroaromatic molecule and a model for the photochemical

158 etecting aqueous 2,4-dinitrotoluene (DNT), a nitroaromatic molecule very similar to TNT, as well as T

159 on, orientation, and SERS detection limit of nitroaromatic molecules in aqueous solutions.

160 Detection of nitroaromatic molecules, such as nitrobenzene (NB), 2,4-

161 ectroscopy of the peptoids revealed that the nitroaromatic monomer has a significant effect on peptoi

162 and characterization of peptoids containing nitroaromatic monomer units.

163 rates of MCs and their surrogates including nitroaromatics [NACs; 2,4,6-trinitrotoluene (TNT), 2,4-d

164 ant substances in aqueous solution including nitroaromatics, neurotransmitters, amino acids, and nucl

165 the reduction of three classes of MCs (poly-nitroaromatics, nitramines, and azoles) by hematite or g

166 igated for the direct determination of trace nitroaromatics, nitrate esters, and nitramine explosives

167 ng mechanism in the reductive cyclization of nitroaromatics, non-nitrene pathways have only been theo

168 e, fast, and facile quantitative methods for nitroaromatic OP compounds.

169 finity of zirconia for the phosphoric group, nitroaromatic OPs strongly bind to the ZrO(2) nanopartic

170 d to electrochemically sense the presence of nitroaromatics owing to the selective ability of nitroar

171 We have designed a nitroaromatic photochemical protecting group that absorb

172 trimers making face-to-face contact with the nitroaromatic portion of the electron acceptor.

173 The reaction for a series of substituted nitroaromatics proceeded by reduction, as indicated by f

174 Nitroaromatic prodrugs are used to treat a range of micr

175 EPT) applications as a activating enzyme for nitroaromatic prodrugs of the dinitrobenzamide class.

176 and NO(2) addition leads to light-absorbing nitroaromatic products.

177 Nitroaromatics quench the fluorescence of Zn(salicylaldi

178 catalyze the oxygen-insensitive reduction of nitroaromatics, quinones, and riboflavin derivatives.

179 sually respond to a class of analytes (e.g., nitroaromatics), rather than a single specific target.

180 olitin family, not previously identified for nitroaromatic recognition, allows near-infrared fluoresc

181 ombination of two physical properties of the nitroaromatics: redox potential and log P.

182 agents were placed in separate compartments, nitroaromatic reduction only occurred when sulfides were

183 ncentrations because NOM was recycled by the nitroaromatic reduction.

184 This process can be applied as a nitroaromatic remediation strategy, provided that a quin

185 opropane carboxylic acids substituted with p-nitroaromatic rings.

186 The array was able to discriminate unknown nitroaromatic samples in solution.

187 Additional experiments revealed that nitroaromatic side chains can influence peptoid nonamer

188 Building upon our understanding of simpler nitroaromatic species, and using linear-response time-de

189 In response to the binding of specific nitroaromatic species, such peptide-nanotube complexes f

190 based on the oxygen-dependent reduction of a nitroaromatic spiroadamantane 1,2-dioxetane scaffold.

191 rofurazone as substrate, leading to reversed nitroaromatic substrate selectivity for the double and t

192 on to the reaction rate varies for different nitroaromatic substrates of NBDO and 2NTDO.

193 lide from a variety of electrophilic aza- or nitroaromatic substrates to form O(2)-arylated derivativ

194 rotein that reduces a variety of quinone and nitroaromatic substrates.

195 rotein that reduces a variety of quinone and nitroaromatic substrates.

196 ction limit of 39 or 48 ppb along with other nitroaromatics such as p-nitrotoluene and p-nitrophenol.

197 quinone respiration expanded the spectrum of nitroaromatics susceptible to transformation.

198 Without quinones, no nitroaromatic tested was reduced except for the IMC 3-ni

199 Sensitivities of the clones to 11 HAP (six nitroaromatics, three benzotriazine N-oxides, and two qu

200 their ability to detect nitramine (RDX) and nitroaromatic (TNT) explosives.

201 s were performed, using three classes of MC (nitroaromatic [TNT, DNAN], nitramine [RDX], and azole [N

202 oaromatics owing to the selective ability of nitroaromatics to decouple the inhibition of pyruvate me

203 cae (NR) catalyzes two-electron reduction of nitroaromatics to the corresponding nitroso compounds an

204 ases have rarely supported full reduction of nitroaromatics to their amine products, and more typical

205 ed to the peptide Bombolitin II to recognize nitroaromatics via infrared fluorescent emission, and po

206 Biotransformation of nitroaromatics via microbial respiration has only been r

207 Nitrated organic compounds, particularly nitroaromatics, were identified as the main products tha

208 ) sensor array that accurately discriminated nitroaromatics, which are mimics of plastic explosives.