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1 by ascorbate + TMPD (N,N,N',N'-tetramethyl-p-phenylenediamine).
2 by ascorbate/TMPD (N,N,N',N'-tetramethyl-1,4-phenylenediamine).
3 yoglobin-imprinted electropolymerized poly(o-phenylenediamine).
4 was circumvented by replacing XY=en with 1,2-phenylenediamine.
5 ly initiated reaction with aqueous diethyl-p-phenylenediamine.
6 oss sections of the optic nerve stained with phenylenediamine.
7 lycerophosphate, and N,N,N',N'-tetramethyl-p-phenylenediamine.
8 nor system ascorbate-N,N,N',N'-tetramethyl-p-phenylenediamine.
9 corbate and the electron donor tetramethyl-p-phenylenediamine.
10 nsation of the oxidation products with ortho-phenylenediamine.
11 nediamine subunit compared to that of free p-phenylenediamine.
12 is is commonly associated with exposure to p-phenylenediamine.
13 also inhibited when N,N,N',N'-tetramethyl-p-phenylenediamine (0.5 mM) and ascorbate (5 mM) were used
14 of doubly trimethylene-bridged tetrabenzyl-p-phenylenediamine 1(Bz) in its singly and doubly charged
15 HC diet plus the antioxidant N',N '-diphenyl-phenylenediamine (1%), the extent of lesion involvement
16 zylene 2 as corner unit with 12 equiv of 1,4-phenylenediamine 3a or benzidine 3b as spacers yields na
17 with the substrate analogs 4,5-dimethyl-1,2-phenylenediamine, 4-methylcatechol, indole, 3,4-dimethyl
18 (ADC) consisting of auristatin phenylalanine phenylenediamine (AFP) or monomethyl auristatin phenylal
19 starting material, which on reacting with o-phenylenediamine and 1,10-diaminonaphthalene afforded hi
20 etween triethylene glycol functionalized 1,2-phenylenediamine and 2,9-diformylphenanthroline subcompo
22 spray detection with N,N,N',N'-tetramethyl-p-phenylenediamine and densitometric scanning of the purpl
23 lted in either a loss or retention of both p-phenylenediamine and ferroxidase activities, indicating
25 ring is demonstrated using the reaction of p-phenylenediamine and isobutyraldehyde to form the diimin
27 butylated hydroxytoluene and N,N'-diphenyl-p-phenylenediamine and the iron chelator deferoxamine.
28 tions, which engage commercially available o-phenylenediamines and o-cyanobenzaldehydes, are discusse
29 tional redox mediator, 2,3,5,6-tetramethyl-p-phenylenediamine, and presents superb energy density as
30 ble of oxidizing other substrates, such as p-phenylenediamine, and there is still a question of wheth
33 mpared to those of the linear tetra-phenyl-p-phenylenediamine as well as the tetra-p-anisyl-p-tetraaz
35 th aqueous ammonia to give the corresponding phenylenediamines can be achieved by using a dicopper co
36 are derived from cholic acid, lysine, and p-phenylenediamine, can produce pores in lipid bilayers as
37 mpling, derivatization with 4,5-dimethyl-1,2-phenylenediamine, capillary electrophoresis separation,
39 ries of potent 5-LOX inhibitors containing a phenylenediamine core, were synthesized that exhibit nan
43 imple condensation between either isomers of phenylenediamine derivatives or 1,3,5-benzenetriamine an
46 mine (DA), tyrosine (Tyr) and N,N-dimethyl-p-phenylenediamine (DMPA), were evaluated using methanol/w
47 formed radicals converted the N,N-dimethyl-p-phenylenediamine (DMPD) probe to the colored DMPD(+) rad
48 terized DbetaM reductant, N,N-dimethyl-1,4-p-phenylenediamine (DMPD), were parallel to the ascorbic a
50 esponse of a 10% (by weight) N,N'-diphenyl-p-phenylenediamine (DPPD) and 90% (by weight) carbon and b
51 ability of the antioxidant N,N'-diphenyl-1,4-phenylenediamine (DPPD) to protect the t-bOOH treated ce
52 ectrochemically deposited ferrocene-modified phenylenediamine film on a glassy carbon electrode is re
53 ichloro-, 2,6-dichloro-, and 4,5-dibromo-1,2-phenylenediamine, followed by oxidation with hot acidic
54 th 1,2-diaminobenzene derivatives, such as o-phenylenediamine, followed by quantification of the resu
55 e by this in situ generated 4,5-dimethyl-1,2-phenylenediamine gave rise to the observed 2,3,6,7-tetra
58 Ms of N,N,N'-trimethyl-N'-(10-thiodecyl)-1,4-phenylenediamine (I) and bis(10-(2-((2,5-cyclohexadiene-
59 es including benzimidazole, 4,5-dimethyl-1,2-phenylenediamine, imidazole, histidine, adenine, and gua
60 ption rate supported by 0.4 mM tetramethyl-p-phenylenediamine in antimycin-inhibited uncoupled intact
61 also been reported recently, including para-phenylenediamine in henna tattoos, cocamidopropyl betain
62 artificial reductant N,N,N',N'-tetramethyl-p-phenylenediamine in place of ubiquinol was, however, uni
63 f-produced coreactant H2O2 was consumed by o-phenylenediamine in the presence of enzyme, effectively
64 excellent peroxidase mimetic activity with O-phenylenediamine in the presence of hydrogen peroxide.
65 between hydrogen sulfide and N,N-dimethyl-p-phenylenediamine in the presence of iron(III) chloride t
66 transfer upon addition of a second bridging phenylenediamine is a consequence of a decrease in the b
68 re coated with a permselective Nafion-Poly(o-phenylenediamine) layer and cross-linked to l-glutamate
69 h biosensors that were protected by a poly(m-phenylenediamine) membrane deposited onto the platinum e
70 ands containing catechol, o-aminophenol or o-phenylenediamine moieties show great potential to be exp
72 attached with a dansyl group, in which the p-phenylenediamine moiety serves as electron donor and the
76 chip by oxidative electropolymerization of m-phenylenediamine (mPD) in the presence of SMZ, acting as
79 oxyaniline- N, N, O-trisacetic acid, and 1,2-phenylenediamine- N, N, N', N'-tetrakisacetic acid are r
80 roxyaniline- N, N, O-trisacetic acid and 1,2-phenylenediamine- N, N, N', N'-tetrakisacetic acid-funct
81 ment of ds-DNA and Au nanoparticles in the o-phenylenediamine network via one-step electropolymerizat
82 ic oxide (NO.) sensors were prepared using o-phenylenediamine (o-PD) and Nafion to modify the surface
85 r was prepared by electropolymerisation of o-phenylenediamine (o-PD) on a gold electrode in the prese
86 fion and electropolymerized polyeugenol or o-phenylenediamine on 30-microm carbon fiber disk electrod
89 from deproteinized tissue extractions were o-phenylenediamine (OPD) derivatized, ethyl acetate extrac
90 5, 5'-tetramethylbenzidine (TMB) and omicron-phenylenediamine (OPD) in the presence of hydrogen perox
91 )-containing PD fluids (pGDPs) by applying o-phenylenediamine (OPD) to form stable derivatives, which
92 e classic chromogenic (UV-vis) assay using o-phenylenediamine (OPD) was also adapted to microtiter pl
95 tz and aerial oxygen, aldehyde reacts with o-phenylenediamine or o-aminothiophenol under visible ligh
96 s locus displayed an N,N,N',N'-tetramethyl-p-phenylenediamine oxidase-negative phenotype, elicited th
97 coupled to quinol or N,N,N',N'-tetramethyl-p-phenylenediamine oxidation, and the activity was sensiti
98 of 1,3,5-triformylphloroglucinol (Tp) with p-phenylenediamine (Pa-1) and 2,5-dimethyl-p-phenylenediam
99 p-phenylenediamine (Pa-1) and 2,5-dimethyl-p-phenylenediamine (Pa-2), respectively, in 1:1 mesitylene
101 e electrochemical biosensors based on poly(o-phenylenediamine) (PoPD) and acetylcholinesterase (AChE)
102 e ss-ODN was washed out of the ss-ODN/poly(o-phenylenediamine)(PoPD)/ITO electrode using sterilised b
103 aim of this study was to determine whether p-phenylenediamine (PPD) and/or Bandrowski's base (BB) sti
105 croelectrode with an electrodeposited poly-m-phenylenediamine (PPD) layer and an R. gracilis D-amino
110 ted phenazines as major products, N-phenyl-o-phenylenediamine produces polycyclic aromatic heterocycl
111 The lipophilic antioxidant N,N'-diphenyl-p-phenylenediamine protected TLF-1-treated T. brucei bruce
112 the substituent on the N that is part of the phenylenediamine redox couple and R indicates the substi
114 eptors, 1-4, based on the incorporation of p-phenylenediamine(s) within a urea framework, were synthe
115 d indirect-acting mutagens, namely 4-nitro-o-phenylenediamine, sodium azide, mitomycin C, benzo[a]pyr
116 of PPD to cells and serum, did not prevent p-phenylenediamine-specific stimulation of patient lymphoc
117 th in the optic nerve was quantified by para-phenylenediamine staining, and a complete blood count sy
118 d electron-transfer sensors were made from p-phenylenediamine-substituted azacrown ethers attached wi
119 increase in the oxidation potential of the p-phenylenediamine subunit compared to that of free p-phen
120 similar conformations as the other dimeric p-phenylenediamines, such as derivatives 1(Me) and 1(Et),
121 unsymmetrically functionalized tetraalkyl-p-phenylenediamine (TAPD) units which are difficult to syn
122 ut also its conversion into 4,5-dimethyl-1,2-phenylenediamine through Strecker-type transformations.
123 (2+)-chelating motifs (hydroxamic acid and o-phenylenediamine) through aromatic omega-amino acid link
124 tric method, using N,N,N',N'-tetramethyl-1,4-phenylenediamine (TMPD) as a pi-donor, was used to rank
126 able finding is the ability of tetramethyl-p-phenylenediamine (TMPD) to oxidize (interrogate) H(ads)
128 n A and cyanide, and N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD) was oxidized by antimycin A-pois
129 he radical cation of N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD), formed through oxidation by (3)
130 ical electron donor, N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD), may overcome the resistance of
132 by its postincubation derivatization with o-phenylenediamine to form a product amenable to fluoresce
133 ethylpiperidinyloxy) and then reacted with o-phenylenediamine to form the condensation product, 3-(di
134 idative condensation of syringaldehyde and o-phenylenediamine to give 2-(3,5-dimethoxy-4-hydroxypheny
135 one, and threosone in the human lens using o-phenylenediamine to trap both free and protein-bound add
137 decomposition and glyoxylate reaction with o-phenylenediamine to yield a quinoxalone that was detecte
141 rom N,N'-bis(carboxymethyl)-N,N'-dinitroso-p-phenylenediamine using an assay that combines catalase w
142 r by ascorbate plus N,N,N', N'-tetramethyl-p-phenylenediamine via cytochrome c1 and the iron-sulfur p
143 were synthesized from the corresponding 1,2-phenylenediamines via successive cyclization with cyanog
144 n pre-column derivatisation with 4-methoxy-o-phenylenediamine was adopted, yielding the method quanti
145 dox reactions of ferrocene and tetramethyl-p-phenylenediamine were obtained in supercritical CO2 in t
146 exes (salophene = N,N'-bis(salicylidene)-1,2-phenylenediamine) were synthesized and evaluated for bio
147 ficiently promote the cyclocondensation of o-phenylenediamine with aldehydes to afford selectively th
149 ay-containing ATPS to catalyze reaction of o-phenylenediamine with peroxide to form 2,3-diaminophenaz
150 enerally accomplished by condensation of 1,2-phenylenediamines with substituted phenyloxoacetates.
151 sfer complex (TMPD = N,N,N',N'-tetramethyl-p-phenylenediamine) with a 1.492 (2) A central sp(2)[bond]
152 The intermediate was trapped with ortho-phenylenediamine, yielding a stable quinoxaline derivati
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