ライフサイエンスコーパス: dication

1 eutral) and |g| = 0.005 at 385 nm (diradical dication).

2 to amine alpha,alpha'-dications (2-azaallyl dications).

3 can be assigned as the cation radical or the dication.

4 BPQT(2(*+)) ring is oxidized to the BIPY(2+) dication.

5 also reduced simultaneously to the diradical dication.

6 C diprotonated to give an oxonium-annulenium dication.

7 antially greater than that of the butadienyl dication.

8 th the very small hydrogen atom or beryllium dication.

9 producing an electroactive 4,4'-bipyridinium dication.

10 t-3-yl)-2,3,5,6-tetramethylb enzene-1,4-diyl dication.

11 lectronic reduction of the 4,4'-bipyridinium dication.

12 e preserve of uranium-nitrides or the uranyl dication.

13 involving the neutral organic donor and its dication.

14 ion as well as a rare example of a noble-gas dication.

15 8 kcal/mol more stable than the closed-shell dication.

16 escales before the break-up of the molecular dication.

17 ions on the structural features of diradical dication.

18 ve rise to the formation of weakly diatropic dications.

19 transformed into superelectrophilic amidine dications.

20 reaction with tris-phenanthroline magnesium dications.

21 ligands linked by [K(2)(18-crown-6)(2)](2+) dications.

22 d molecular chlorine (Cl2) and bromine (Br2) dications.

23 try of the corresponding radical cations and dications.

24 are hybrids of pyrylium cations and Viologen dications.

25 ris(dialkylamino)cyclopropenium (CP) radical dications.

26 lectronic features in the resulting mono and dications.

27 ies of aromatic and antiaromatic cations and dications.

28 Further oxidation gives stable dications.

29 the formation of spectroscopically distinct dications.

30 ticity of the fluorenyl ring system of these dications.

31 tion that is typical of "superelectrophilic" dications.

32 ility of the corresponding aminium diradical dications.

33 es compared to the corresponding symmetrical dications.

34 The corresponding dications 1(2+)-4(2+) show a complementary trend in the

35 overed by these studies are the bifunctional dications 1,8-bis(xanthylium)-biphenylene ([3](2+)) and

36 The antiaromaticity of fluorenylidene dications 1-5, which contain cyclic cationic substituent

37 Dication (1(2+)) reacts with fluoride to afford [1-F]+ w

38 esonance energies of the trimethylenemethane dication (1) and the butadienyl dication (4) were evalua

39 by 2 equiv of acetylferrocenium afforded the dication [1](2+), which, on the basis of low-temperature

40 and (CF(3)CO)(2)O affords the corresponding dication, 1,8-bis(diphenylmethylium)naphthalenediyl (1(2

41 The dications, 10a, 10d, 10f, and 10g are more active than f

42 The 1,3-adamantanediyl dication 1b with two bridgehead tertiary carbocationic c

43 ridyl)biphenyl with 1-bromooctane yields the dication 2(2+) 2Br-, an "extended viologen" isostructura

44 The LUMO of the dimer dication 2(2+) is metal-metal antibonding, and its half-

45 ntial (E(1/2) = 0.47 V) to the corresponding dication 2(2+).

46 and crystallographic characterization of the dications 2(2+) and 6(2+) (as [PF(6)](2) salts) and 4(2+

47 synthetic equivalents to amine alpha,alpha'-dications (2-azaallyl dications).

48 The C-C protonated 1-adamantyl dication, 2f, was characterized as the most stable struc

49 The dication 3 2+, with strongly deshielded internal methyls

50 In the gas phase, the diphosphonium dication 3(2+) has similar energy to two [PMe3](+) radic

51 e dianion (2) and the antiaromaticity of the dication (3) of tetrabenzo[5.5]fulvalene have been evalu

52 Dications 32, 64, and 66 exhibited antitrypanosomal pote

53 Dications 3a and 6a have substantial kinetic barriers fo

54 protonated chlorine and diprotonated bromine dications 3a and 6a, respectively, were found to be lowe

55 Lambda, supported the antiaromaticity of the dications 3a-f(2+).

56 The isomeric dications, 3b and 6b, are also minima on the potential e

57 Dimethylated molecular chlorine and bromine dications 3g and 6g, respectively, were also found to be

58 ylenemethane dication (1) and the butadienyl dication (4) were evaluated using two independent comput

59 o-, m-, and p-phenylene bis(1,3-dioxolanium) dications (4-6) and 2,4,6-triphenylene tris(1,3-dioxolan

60 ed to give paratropic carboxonium-annulenium dications (4H2 2+, 5H2 2+, 6H2 2+, and 7H2 2+, respectiv

61 The dianion, 5(2-), and dication, 5(2+), of tetrabenzo[5.7]fulvalene represent a

62 en the electrons of the triplet state of the dication 6(2+), calculated from its dipolar EPR splittin

63 Tf to the corresponding radical cation 6 and dication 7 in-situ.

64 Similarly, the formation of the dication 7 is inferred by its ready elimination of isobu

65 The reaction of dication 8 with 6 in the presence of Me3SiOTf gave an io

66 and cathodic pulses, while for anion (A(-*))-dication (A(2+*)) annihilation, transient ECL shows asym

67 The dication ABA(2+) and dianion ABA(2-) are open-shell sing

68 While many dications act as purely competitive inhibitors, some fai

69 The unsymmetrical dications allowed sensitive detection for these anions w

70 t side reactions in less stable antiaromatic dications, allowing exploration of a number of species t

71 orm crystals in which the layers of viologen dications alternate with those of a 1:2 supramolecular c

72 Here we report that the large dication aminomethylpyridinium (AMPY) can template novel

73 hell singlet diradicaloids, while the longer dication ANA-TFA(2+) and dianion ANA(2-) have closed-she

74 The monocation and dication analogues {[(BDI)(N(t)Bu)Nb]2(mu-eta(3):eta(3)P

75 relation between the redox potential for the dication and both the calculated NICS and sigma(m).

76 calculated difference in energy between each dication and its neutral precursor.

77 rily reflect the magnetic properties of this dication and potentially those of the other dications st

78 of TTF+* to form the diamagnetic [TTF+,TTF+] dication and to also undergo the equally rapid cross-ass

79 relative stability of doubly charged alkane dications and monocharged boron cation analogues are dis

80 nd in the oxidized species (radical cations, dications and radical trications) has been investigated,

81 to include hypercoordinated onium-carbonium dications and the isoelectronic onium-boronium cation an

82 similar to a band seen in the corresponding dications and to that observed in the monocation of a mo

83 ise oxidation to the radical cations and the dications and was found to be remarkably large (19% and

84 irectly competing for PLGA interactions with dications and/or b) increasing peptide affinity in the s

85 (assigned to the formation of the cation and dication) and a two-electron reduction wave that becomes

86 three chromophores, the radical cation, the dication, and the pi-dimer have been identified and char

87 ix compounds will lose two electrons to form dications, and the use of suitable oxidizing agents has

88 r the radical anion-cation and radical anion-dication annihilation, respectively.

89 Charge repulsion in the dication apparently keeps it from forming the dimer.

90 risulfide is formed by reaction of the dimer dication [Ar4S4](2+) with neutral Ar2S2 to afford the tr

91 A dimer dication, [Ar4S4](2+), is proposed as an intermediate in

92 The monocation and dication are both stable, as demonstrated by optical stu

93 esence of trifluoroacetic acid, C-protonated dications are generated.

94 The dications are globally aromatic while the tetracations a

95 l derivative, the redox potentials for these dications are less positive than for formation of the di

96 Heterocyclic dications are receiving increasing attention as targeted

97 thesized using a new ditetraalkylphosphonium dication as an organic structure-directing agent, and it

98 mily of asymmetric peptide linked diaromatic dications as potent DNA minor groove binders.

99 orporating a series of bifunctional ammonium dications as templates which also emit white light: (1)

100 The dication binds to both sequences in monomer complexes bu

101 )NH(2)(+)CH(2)) and the other a bipyridinium dication (BIPY(2+)).

102 function and form, as this uniquely compact dication boasts more heteroatoms than carbon centers.

103 Addition of TFA gave the related dications, but these exhibited significantly reduced aro

104 is supported by the direct observation of a dication by low-temperature (13)C NMR.

105 ted carboxylic acid 9 gives a mixture of two dications by CO and ring protonation.

106 ds 1-CS and 2-OS can be oxidized into stable dications by FeCl(3) and/or concentrated H(2)SO(4).

107 gas phase with tris-phenanthroline magnesium dications by forming [FA - H + MgPhen](+) complex ions.

108 Structures of the isomeric adamantanediyl dications C(10)H(14)(2+) and protio-1- and protio-2-adam

109 14)(2+) and protio-1- and protio-2-adamantyl dications C(10)H(16)(2+) were investigated by using the

110 ative study of the superelectrophilic alkane dications (C(n)H(2n+2)2+), n = 1-5) and their isoelectro

111 A highly Lewis acidic diphosphonium dication [(C10H6)(Ph2P)2](2+) (1), in combination with a

112 ifs of planar methane and the planar methane dication can be extended to give planar hypercoordinate

113 The 2,9-dimethyldiazaperopyrenium dication can be made from a ubiquitous and inexpensive f

114 These dications can be modified in ways that help illuminate f

115 Their dications can be regarded as the isoelectronic structure

116 pological changes antiparasitic heterocyclic dications can have on kinetoplast DNA, we have construct

117 of the ditosylate Ni(OTs)(2)(dppe) gave the dication [(CO)(2)(dppe)Fe(pdt)Ni(dppe)](OTs)(2) ([2(CO)]

118 dication (DC9) and to identify linked lipid-dication compounds formed.

119 The use of en dication creates a three-dimensional (3D) hollow inorgan

120 '-dimethyl-2,6-diaza-9,10-anthraquinonediium dication (DAAQ.2BF4(-)) exists in equilibrium with both

121 and two more highly conjugated diazapyrenium dication (DAP(2+)) units, respectively, a consecutive se

122 *+)) and an asymmetric cyclophane bisradical dication (DAPQT(2(*+))), affords a symmetric [2]catenane

123 e phenylfuran-benzimidazole unfused aromatic dication DB293 was identified as the first diamidine cap

124 rometry (MS/MS) was used to characterize the dication (DC9) and to identify linked lipid-dication com

125 were more active than pentamidine, and seven dications demonstrated increased activities against P. f

126 the absence of the methoxy substituents, the dication derived from tetraphenylbenziporphyrin 8H2(2+)

127 tructures and energies of superelectrophilic dications derived by protonation of methyl- and dimethyl

128 switch consisting of a linked bis(viologen) dication diradical that can be cycled reversibly between

129 crucially affects the subtle balance between dication dissociation under maintenance of the 2-fold ch

130 ining the oversized ethylenediammonium ( en) dication, { en}FA(0.5)MA(0.5)Sn(0.5)Pb(0.5)I(3) (FA = fo

131 Eight dications exhibited antitrypanosomal activities comparab

132 Several dications exhibited superior antiplasmodial and antileis

133 e bond positional isomers of charge inverted dication.FA complexes and the subsequent implementation

134 on to other basic sites in the model peptide dication, facilitating exothermic proton transfer from o

135 The computational results indicate that the dications favor 23-atom 22pai electron delocalization pa

136 ns resulted instead in a set of antiaromatic dications from oxidation of fluorenylidene derivatives.

137 This dication has been fully characterized, and its structure

138 polar splitting, the trishydrazine diradical dication has its remote hydrazine units oxidized, althou

139 The dication has undergone C-protonation at one of the meso-

140 Several dications have also been studied.

141 Each of these reacts with transition metal dications having a preference for octahedral coordinatio

142 re further utilized to reduce hexyl-viologen dication (HV2+) and a sacrificial electron donor, 1-benz

143 (1,4,5,8-tetraazaphenanthrene)]ruthenium(II) dication immobilized on alkali-treated silica microspher

144 omatic 2pai-electron tetrasilacyclobutadiene dication in [(L(Ph)Si)(4)](BPh(4))(2) (L(Ph) = PhC(NtBu)

145 ular structure reveals a four-membered Si(4)-dication in an almost perfect square-planar geometry.

146 The estimated pKa of MDP dication in H2O, 21.2 at 25 degrees C and I = 1.0 M (KCl

147 t sub-100 fs isomerization time on acetylene dication in lower electronic states is not possible and

148 connectors and 6 equiv of a platinum linker dication in nitromethane is presented.

149 ved transient absorption signal for ethidium dication in poly(dG-dC) confirms that guanine oxidation

150 5 H5 ) to oxo-bind and reduce the uranyl(VI) dication in the complex [(UO2 )(THF)(H2 L)] (L="Pacman"

151 The dication in the hydrolysis product [Tl4(mu3-OH)2][H2N{B(

152 to photochemically reduce the hexyl viologen dication in the presence of a sacrificial electron donor

153 Further oxidation to the dication in the presence of ethylene by chemical or elec

154 (bipy(R))Au(mu-O)(2)Au(bipy(R))](2+) as free dications in the gas phase.

155 curately modeled the energies of a series of dications including fluorenylidene dications whose UV-vi

156 tics are governed by the long-range electron-dication interaction and are not affected by side chain

157 ly oxidized to form a cyclopropenium radical dication intermediate.

158 utanediylbis[tris(dimethylamino)]phosphonium dication is a very efficient OSDA for crystallization of

159 The resonance energy of each dication is computed as the difference between the most

160 enantiomerically enriched triplet diradical dication is configurationally stable for 48 h at room te

161 at higher acid concentrations a nonaromatic dication is generated.

162 The diradical dication is monomeric in dibutyl phthalate (DBP) matrix

163 hetic and structural studies showed that the dication is readily reduced to a neutral, singlet bis-1,

164 icon analogue of the aromatic cyclobutadiene dication is reported.

165 ent binding pocket wherein a methyl viologen dication is stabilized by interacting with a bipyridiniu

166 resonance energy of the trimethylenemethane dication is substantially greater than that of the butad

167 a doubly ag conformation, and its diradical dication is suggested to be a triplet because it does no

168 The fragmentation dynamics of the dication is unraveled by the use of advanced ion and ele

169 fragmentation behavior of the mass-selected dications is probed by means of collision-induced dissoc

170 oxidant AgBF4 formed the metal-free radical dication L(.2+) .

171 oupling between the coordinated paramagnetic dication (M) and nitroxide (NIT) unit.

172 1,1'-Methylenebis(pyridinium) dication (MDP) is an unusual ion with two formal positiv

173 The dications Me3C2+ and Et3C2+ have optical spectra that ap

174 he reversible insertion of a large molecular dication, methyl viologen, into the crystal structure of

175 GSL-H](-), and terpyridine-magnesium complex dications, [Mg(Terpy)(2)](2+), are sequentially injected

176 With methyl viologen dication (MV(2+)) added as a trap, Acr-(3)An + MV(2+) --

177 hers phenol and 1,1-dimethyl-4,4'-bipyridine dication (MV(2+)).

178 mplex of the N,N'-dimethyl-4,4'-bipyridinium dication (N,N'-dimethyl viologen, MeV) suggests that the

179 molecular recognition between the bisradical dication obtained on reduction of the tetracationic cycl

180 stallographically characterized salts of the dications obtained by two-electron oxidation of E-4,4'-b

181 and T6, whereas subsequent oxidation to the dication occurs more easily for TPTTPT than for TPEEPT a

182 The vis-NIR absorption of the dication of (E,E)-1,4-bis{4-[bis(4-n-butoxyphenyl)amino]

183 The doubly oxidized diradical dication of 1(Bz) exists in the spin-paired singlet stat

184 ical oxidation with SbF(5)/SO(2)ClF gave the dication of 9-[(4-methoxyphenyl)methylene]-9H-fluorene c

185 We report an air-stable diradical dication of chiral D(2)-symmetric conjoined bis[5]diazah

186 Derivatives of the dication of tetrabenzo[5.5]fulvalene were prepared with

187 istent with the behavior of the antiaromatic dication of tetrabenzo[5.5]fulvalene, compared to that o

188 nter-naphthalene distance of the dianion and dication of the cyclophane 14 compared to that of its ne

189 The diprotonated dication of this system retains porphyrin-like propertie

190 The greater instability of dications of 2a-g and 3a-g compared to the reference sys

191 tions of 3a-g are more antiaromatic than for dications of 2a-g, which is consistent with their greate

192 are less positive than for formation of the dications of 3a-g and for dications of p-substituted dip

193 The NICS values for dications of 3a-g are more antiaromatic than for dicatio

194 istent with their greater instability of the dications of 3a-g.

195 Redox potentials for formation of dications of analogously substituted tetraphenylethylene

196 The dications of benzylidene fluorenes were less stable than

197 The dications of CBN1 and CBN2, and the tetracation of CBN2,

198 zylidene fluorenes were less stable than the dications of diphenylmethylidene fluorenes; within each

199 The redox potentials for formation of the dications of meta-substituted diphenylmethylidenes (3a-g

200 Dications of p-substituted 3-phenylindenylidenefluorenes

201 r formation of the dications of 3a-g and for dications of p-substituted diphenylmethylidenefluorenes,

202 are more positive than for the formation of dications of para-substituted diphenylmethylidenes (2a-g

203 Mixed dications of PEG that have the same nominal mass but dif

204 The dications of the 22-acetoxybenziporphyrins also show sim

205 deposition apparatus constructed previously, dications of the cyclic peptide Gramicidin S (GS) and th

206 the monomeric two-electron oxidized product (dication) of 1,5-tellurathiocane are reported.

207 on mass spectrometry (DESI-MS) with a stable dication on biological tissues.

208 ered ring mesocycles with NOPF6 or Br2 gives dications or a bicyclic dibromide, respectively, which c

209 various iron(IV)-oxo complexes generated as dications or monocations (bearing an anionic ligand).

210 On treatment with nucleophiles, mesocyclic dications, or the corresponding radical cations undergo

211 maticity of the 3-phenylindenylidenefluorene dications over the unsubstituted indenylidenefluorene di

212 results, collisional activation of cesiated dications overwhelmingly results in ejection of Cs(+).

213 We also find that the dication possesses a large degree of diradical character

214 The diradical dication possesses closed-shell (Kekule) resonance forms

215 MOF-1001 is capable of docking paraquat dication (PQT2+) guests within the macrocycles in a ster

216 eoretical study of the dynamics of acetylene dication produced by Auger decay after X-ray photoioniza

217 On the other hand, the dications produced in TFA-chloroform solutions showed mo

218 haracterization of phenyl viologen (PV) as a dication, radical cation, and neutral species are descri

219 ization of the radical cation gave the dimer dication, [Re2Cp(gamma)2(CO)6]2+ (where Cp(gamma) repres

220 cetylene [HCCH](2+) to vinylidene [H2CC](2+) dication remains nebulous.

221 s, based on the planar preference of methane dications, replace two remote carbons in spiroalkaplanes

222 intended to form three-dimensional aromatic dications resulted instead in a set of antiaromatic dica

223 otonation state from a neutral molecule to a dication results in dramatically increased efficiency of

224 joined bis[5]diazahelicene and its diradical dication show strong chirooptical properties that are co

225 sus the calculated energy difference for the dications showed a moderate degree of linearity; the plo

226 Proton NMR spectra for the dications showed the presence of enhanced diamagnetic ri

227 oxidation, a measure of the stability of the dications, showed a good linear relationship with anothe

228 This feature manifests itself in the uranyl dication showing little propensity to partake in the man

229 Comparison with related dications shows that furamidine inhibits Tdp1 more effec

230 , by adding nucleophiles to an iron(III) pai-dication species formed via addition of trifluoroacetic

231 ing stepwise formation of radical cation and dication species in solution.

232 demonstrate the chemical consequences of the dication stabilities Te(+)-Te(+) > Se(+)-Se(+) > S(+)-S(

233 dication and potentially those of the other dications studied.

234 y identical rates of electron capture by the dications substituted by the benzyl (EA = -1.15 eV) and

235 il interacts cooperatively with bipyridinium dications substituted on their nitrogen atoms with 2-azi

236 e p-methoxy-substituted benzylidene fluorene dication suggests that the calculations satisfactorily r

237 sequence employs nitroalkenes as latent 1,2-dication synthons providing a novel access to highly use

238 migrations occurring in ethanol cations and dications take place within a few hundred fs to ps, usin

239 that the dissociation dynamics of adamantane dications takes place in a two-step process: barrierless

240 ) results in the formation of fluorenylidene dications that are shown to be antiaromatic through calc

241 alenes by SbF(5) results in the formation of dications that behave like two antiaromatic fluorenyl ca

242 However, addition of TFA gave dications that showed far more significant shifts that a

243 Addition of TFA gave dications that showed porphyrin-like spectra with Soret

244 In the proton NMR spectrum for the dication, the internal CH was shifted upfield to approxi

245 s are finely regulated by a second magnesium dication, thus coordinating the entry of a magnesium-bou

246 he substrate to the photoexcited TAC radical dication, thus demonstrating a new reactivity mode for t

247 lex formation which reflects the ease of the dication to form stacked dimeric motifs in the DNA minor

248 stants of a bis-(acetylguanidinium)ferrocene dication to various (di)carboxylates were determined thr

249 The dimer dication TPB2+ can be detected only in EC/ESI-MS.

250 fragment predominantly via a novel headgroup dication transfer to the reagent anion.

251 The effect of the dication type, linkage chain, alkyl substituents, and an

252 Some of the dications undergo rearrangement to a more stable pyramid

253 The radical dication undergoes photoexcitation with visible light to

254 e and activation of the water-soluble uranyl dication (UO(2)(2+)) remains a challenging problem, as f

255 the environment predominantly as the uranyl dication [UO2]2+.

256 ne, 4, have been oxidized to their mono- and dications using tris(4-bromophenyl)aminium hexachloroant

257 The antiaromaticity shown by the parent dication was demonstrated for these dications with space

258 a monocation, and in 50% TFA a C-protonated dication was generated.

259 aphenylborate anionic moiety to the viologen dication was observed less than 1 mus after excitation.

260 d soon afterwards, a derivatized ferrocenium dication was only isolated in 2016 and the monoanion of

261 over the unsubstituted indenylidenefluorene dication was supported by (anti)aromatic (de)stabilizati

262 ituted benzylidene fluorenes to antiaromatic dications was attempted by electrochemical and chemical

263 The performance of dications was evaluated for seven selected anions in bot

264 , the indenyl system of indenylidenefluorene dications was less antiaromatic than the fluorenyl syste

265 ocations, and the generation of C-protonated dications was no longer favored due to the presence of e

266 Electrochemical oxidation to dications was successful for benzylidene fluorenes with

267 adducts, the bonds to the single thianthrene dication were (necessarily) cis.

268 barriers in its radical cation and diradical dication were predicted by the DFT computations to be wi

269 der strongly acidic conditions, C-protonated dications were generated with substantial diatropic prop

270 were more potent than pentamidine and seven dications were more effective than artemisinin against P

271 Thirty-nine dications were more potent against P. falciparum than pe

272 spectra of both the classical and pyramidal dications were obtained.

273 The various geminal dications were paired with up to four different anions.

274 These dications were so electrophilic that they underwent in s

275 A series of mono- and dications were synthesized successfully, including previ

276 Protonation affords an aromatic dication where this type of resonance interaction is fav

277 ompetitive effects, we used a combination of dications, which are intrinsically fluorescent and spect

278 acids, lead to intermediate N,C-diprotonated dications, which are involved in reactions with weak nuc

279 r relationship to those of the corresponding dications, which ESR reveals to be singlet species.

280 to the surface activity of the unsymmetrical dications, which results in a concurrent strong partitio

281 protonation, converts back into the starting dication while also releasing H(2)O(2).

282 BPQT(4+) leads to the CBPQT(2(*+)) diradical dication while the P-BIPY(2+) unit is reduced to its P-B

283 series of dications including fluorenylidene dications whose UV-visible spectra are reported, as well

284 ations, the resulting CBPQT(2(*+)) diradical dication will migrate to the BIPY(*+) unit, resulting in

285 hylglyoxal bis(guanylhydrazone) binds as the dication with a 23 microm dissociation constant.

286 Addition of TFA afforded a C-protonated dication with a significantly increased diatropic ring c

287 '-carboxylate,2,2'-bipyri dine)ruthenium(II) dication with n = 2 (2), 3 (3), 4 (4), and 5 (5).

288 he ion pair prior to interaction of the free dication with the host to produce a complex that is not

289 e shortest species is diamagnetic, while the dication with the longest bridge behaves as two essentia

290 tion of benzene yields primarily high-energy dications with a six-membered-ring structure.

291 Protonation of azuliporphyrins affords dications with enhanced diamagnetic ring currents where

292 bstituted phenyl rings were more stable than dications with m-substituted phenyl rings and dications

293 ene fluorenes; within each type of compound, dications with p-substituted phenyl rings were more stab

294 ications with m-substituted phenyl rings and dications with phenyl rings substituted with electron-do

295 ectron-donating groups were more stable than dications with phenyl rings substituted with electron-wi

296 e parent dication was demonstrated for these dications with spacers, although it was attenuated by th

297 f the single-crystalline 1(Bz)(2+) diradical dications with two different in nature counteranions, re

298 cribes the design and synthesis of two novel dications with unsymmetrical structures and their utiliz

299 Here we show that placing the uranyl dication within a rigid and well-defined molecular frame

300 f a monolayer of such indicators, the Ba(2+) dication would be captured by one of the molecules and g