ライフサイエンスコーパス: fullerene

1 orresponding to LUMO energy levels as low as fullerenes).

2 roups, in the double cyclopropanation of [60]fullerene.

3 ivatives on carbon nanomaterials such as [60]fullerene.

4 urring through the inherent chirality of the fullerene.

5 alternating rings on the surface of the [60]fullerene.

6 is insufficient to switch the MX inside the fullerene.

7 addition reactions or the making of pristine fullerenes.

8 he interaction between CNTs and encapsulated fullerenes.

9 led by varying the weight percentages of the fullerenes.

10 Fs) often differs from that in neutral empty fullerenes.

11 on fillers consisting of graphene flakes and fullerenes.

12 s of metal complexes and metal surfaces with fullerenes.

13 lead towards a useful methodology to purify fullerenes.

14 tices of quantum dots, p-block clusters, and fullerenes.

15 her small clusters such as nanomaterials and fullerenes.

16 In early 2019, we reported a non-fullerene acceptor (named Y6) that can simultaneously ac

17 thesis of a new perylenediimide-thiazole non-fullerene acceptor capable of delivering a power convers

18 s, from 2.79 % to 10.51 % for devices with a fullerene acceptor in the active layer, and from 3.89 %

19 rom 3.89 % to 11.04 % for devices with a non-fullerene acceptor in the active layer, demonstrating th

20 R = alkyl substituent) blended with the non-fullerene acceptor ITIC-Th and analyze the effects of su

21 hology measurements by replacing the typical fullerene acceptor with endohedral fullerene Lu3N@PC80BE

22 and self-assembly of thiadiazole-derived non-fullerene acceptors (NFAs) is very critical for elucidat

23 Organic photovoltaics based on non-fullerene acceptors (NFAs) show record efficiency of 16

24 ls using a ternary approach, wherein two non-fullerene acceptors are combined with both a scalable an

25 However, most non-fullerene acceptors can crystallize and destroy devices,

26 Organic solar cells based on non-fullerene acceptors can show high charge generation yiel

27 paration of dimeric AzaBPDI as potential non-fullerene acceptors for organic solar cells.

28 onformation make them good candidates as non-fullerene acceptors in organic solar cells.

29 owever, the single-junction STOPVs utilizing fullerene acceptors show relatively low PCEs of 4%-6% du

30 nventional electron-deficient-core-based non-fullerene acceptors with near-infrared absorption lead t

31 e-property relationships of a library of non-fullerene acceptors, highlighting the important chemical

32 lk heterojunctions between polymer donor and fullerene acceptors, which provide a model system to und

33 of D18-based OSCs is compared with three non-fullerene acceptors, Y6, IT-4F, and IEICO-4Cl, and their

34 IC-2Cl and ITIC-2F, two state-of-the-art non-fullerene acceptors.

35 eficient-core-based fused structure into non-fullerene acceptors.

36 lization of injected electrons, analogous to fullerene acceptors.

37 This bis-fullerene adduct exhibits different cooperativity in bin

38 force, but to be very strongly dependent on fullerene aggregate size and packing.

39 ers have been synthesized as receptors for a fullerene-ammonium salt derivative (1).

40 The PCE of 12.1% is the highest in fullerene and nonfullerene-based single-junction binary-

41 ro-hydrophosphination reaction into free [60]fullerene and sec-phosphine borane amino ester compound.

42 assays, and compared with dodecaglycosylated fullerenes and a monovalent reference.

43 with advances in the synthesis of pure boron fullerenes and atom-thin layers, motivates an exploratio

44 es are considered structural constituents of fullerenes and carbon nanotubes.

45 capsule 1(8+) in the selective separation of fullerenes and endohedral metallofullerenes (EMFs) remai

46 f earlier studies on regioselectivity of IPR fullerenes and endohedral metallofullerenes.

47 ene derivatives or as molecular fragments of fullerenes and graphene nanoribbons.

48 tercalation into PAHs differs from that into fullerenes and graphite, in which the cation sites are p

49 lytic behavior, involving the combination of fullerenes and low-dimensional (LD) nanohybrids, is curr

50 dducts selectively, whereas unfunctionalized fullerenes and monoadducts were not encapsulated.

51 a route to enhance charge delocalization in fullerenes and other organic semiconductors.

52 es that can exceed the device performance of fullerenes and provide opportunities to improve upon the

53 rs by using the specific interaction between fullerenes and saccharides in liquid chromatography (LC)

54 sorbents include activated carbon, biochar, fullerenes, and carbon nanotubes, with applications such

55 ental molecular building block in graphenes, fullerenes, and carbon nanotubes-is facilitated by a bar

56 etal clusters or purely nonmetal cages, like fullerenes, and even noncovalent aggregates such as wate

57 reactions between the two electron-accepting fullerenes, and for kinetics that are influenced by the

58 ive energies of a large number of isomers of fullerene anions, C(2n)(q) (2n = 68-104; q = -2, -4, -6)

59 (biochar) by comparing it with heat-treated fullerene arc-soot.

60 Anion-pi interactions on fullerenes are about as poorly explored as the use of fu

61 ereby yielding materials in which metals and fullerenes are brought together in ordered arrangements.

62 Multi-functionalization and isomer-purity of fullerenes are crucial tasks for the development of thei

63 While fullerenes are known to entrap metal atoms to form endoh

64 Enolate-pi interactions on fullerenes are much shorter than standard pi-pi interact

65 Total synthetic approaches of fullerenes are the holy grail for organic chemistry.

66 This revealed the potential role of fullerene as nanomediator in the signal transduction.

67 ated with peripheral electron donors and [60]fullerene as the acceptor.

68 icipated that this data will position chiral fullerenes as an exciting material class for the growing

69 l electrolyte system, exploiting derivatized fullerenes as both anolyte and catholyte species in a se

70 tation of specific carbohydrates by using 3D fullerenes as controlled biocompatible carbon scaffolds

71 We focus mainly on investigations regarding fullerenes as well as endohedral metallofullerenes in en

72 ullerodendrimers and cysteine-functionalized fullerene assemblies.

73 ns into charge-producing states in a polymer:fullerene based solar cell.

74 A new method for the functionalization of fullerenes based on the reaction between in situ generat

75 carrier blocking layers commonly employed in fullerene-based devices.

76 continuum is without precedent in synthetic fullerene-based dyads.

77 e determine that replacing the commonly used fullerene-based electron acceptor with a perylene diimid

78 signed hosts are able to associate up to two fullerene-based guest molecules and present association

79 y review the synthetic approaches to prepare fullerene-based hybrids with LD (0D, 1D, and 2D) materia

80 Recent advances in the design of fullerene-based LD nanomaterials for (photo)electrocatal

81 tudies are needed to determine the optimized fullerene-based leads for practical applications.

82 Fullerene-based low-dimensional (LD) heterostructures ha

83 The presented organic-fullerene-based material exhibits a non-porous dynamic c

84 omparable to those of the highest-performing fullerene-based materials.

85 Our devices are comparable to the best fullerene-based photodetectors, and the sensitivity at l

86 15 %, which is far above the most efficient fullerene-based PSCs.

87 yses were performed on Shroom3 in mice using fullerene-based siRNA delivery, which demonstrated that

88 e orders of magnitude slower than comparable fullerene-based systems.

89 ing the efficiencies of fullerene-based, non-fullerene-based, and ternary organic solar cells (OSCs)

90 ar orientation, boosting the efficiencies of fullerene-based, non-fullerene-based, and ternary organi

91 The regio- and stereocontrolled synthesis of fullerene bisadducts is a topic of increasing interest i

92 mall molecule acceptor into a P3HT-based non-fullerene blend increases the device efficiency up to 7.

93 A low-bandgap polymer:fullerene blend that has significantly reduced energetic

94 ss transition temperature of ternary polymer/fullerene blend thin films and their constituents, which

95 trafast charge transfer processes in polymer/fullerene blends have been intensively studied but much

96 Here, polymer-fullerene blends with contrasting photocurrent propertie

97 the exciton-dominated pathway in the polymer/fullerene blends.

98 In this study, the fullerene-bonded columns were used to separate saccharid

99 The device efficiency of polymer:fullerene bulk heterojunction solar cells has recently s

100 rmation are not optimal for the formation of fullerenes, but instead, curved carbon structures coales

101 ally, the hydrophosphination reaction of [60]fullerene by the sec-phosphine borane compounds was perf

102 of molecular receptors for the separation of fullerenes by means of host-guest interactions.

103 The impact of fullerene C(60) water soluble daughter molecules - fulle

104 CNB1 demonstrates selective encapsulation of fullerene C(70) over C(60), with a large association con

105 In addition, the encapsulation of bis-aza[60]fullerene (C(59)N)(2) within a supramolecular coordinati

106 = 0, 3, 5), were constructed by linking the fullerene (C(60)) and bis(3,4,5-trimethoxyphenyl)aniline

107 s (MWCNTs), reduced graphene oxide (RGO) and fullerene (C(60)), and show similar effects upon complex

108 (2)) and the primary electron-acceptor C(60)-fullerene (C(60), acceptor(1)) are attached.

109 h epoxy and hydroxy groups on the surface of fullerenes (C(60)) and thereby improve the solubility of

110 Box exhibits strong recognition of pristine fullerenes (C(60/70)), with the noncovalent ground and e

111 of isolated water molecules encapsulated in fullerene-C(60) cages by time-domain terahertz (THz) spe

112 terpret the superstructure composing aqueous fullerene C60 nanoparticles prepared by prolonged stirri

113 formation of aminomethylated derivatives of fullerene C60 with high yields (80-90%) and selectivity

114 host-guest complexes containing 1-4 equiv of fullerene C60, depending on the solvent employed.

115 articular, we focus on dendrimers as well as fullerene C60-with a unique symmetrical and 3D globular

116 uding the ability to co-crystallize with the fullerenes C60 and C70.

117 nd encapsulate large aromatic guests such as fullerenes C60 and C70.

118 e resolved at the zinc phthalocyanine (ZnPc)-fullerene (C60) donor-acceptor interface.

119 g of the three-dimensional potential between fullerene (C60) molecules in different relative orientat

120 A549 cells were treated with fullerene (C60), long or short multi-walled carbon nanot

121 superatom molecular orbitals (SAMOs) of the fullerene cage as a means of Li activation, thereby bypa

122 ture, ultimately leading to the closed-shell fullerene cage C60(-) as preprogrammed by the precursor

123 fullerene CH(4) @C(60) , in which each C(60) fullerene cage encapsulates a single methane molecule, h

124 The addition of solubilizing addends to the fullerene cage results in a large number of isomers, whi

125 e of the addends, and (iv) the variations in fullerene cage stability with the progressive addition o

126 nation of the unique encapsulation effect of fullerene cages and the variable oxidation states of act

127 l atoms have been observed to be part of the fullerene cages.

128 ther the typically favored [6,6]-addition in fullerenes can be shifted to the [5,6] bonds in (#6094)C

129 2F]T polymers are particularly promising non-fullerene candidates for "all-polymer" BHJ solar cells.

130 These signatures include a class of fullerene carbon clusters that we hypothesize represent

131 nt metal-based nanoparticles or nanocarbons [fullerene, carbon nanotubes (CNTs), and graphenes] with

132 he most recent carbon nanostructures, namely fullerenes, carbon nanotubes, and graphene, have receive

133 The endohedral fullerene CH(4) @C(60) , in which each C(60) fullerene c

134 adducts is a topic of increasing interest in fullerene chemistry and a key point for the full exploit

135 contribute not only to the basic science of fullerene chemistry but would also be used towards effec

136 ohedral fullerenes is an important aspect of fullerene chemistry, since the experimentally formed str

137 d become more widely adopted in the field of fullerene chemistry.

138 at the heterojunction and/or the presence of fullerene clusters guarantee efficient CT dissociation a

139 -layer compression of the negatively charged fullerene clusters, and the nC60s and nHOFs alike displa

140 miscibility between this particular polymer:fullerene combination and to co-crystallization of Lu3N@

141 lamide functionalised reduced graphene oxide-fullerene composite and double layered acrylamide functi

142 These fullerene compounds were then reacted with thiol derivat

143 C(60) nanosheets (NSs) within a very narrow fullerene concentration range.

144 o models is comparable with that observed in fullerene-containing materials, which are generally cons

145 l fullerenes in contrast with their pristine fullerene counterparts, (ii) the appearance of more pent

146 form remains elusive, especially for higher fullerenes (Cx, x > 70).

147 terials, mixed metal complexes and clusters, fullerenes, dendrimeric nanocomposites, polymeric materi

148 fects of humic acid on lipid accumulation of fullerene depended on the lipid head charge.

149 A fullerene derivative (alpha-bis-PCBM) is purified from a

150 The water-soluble and fluorescent [60]fullerene derivative (C60-serPF) was designed to be an a

151 h gain is presented based on the polymer and fullerene derivative incorporating inorganic quantum dot

152 value lower than those of the PSCs based on fullerene derivative or organic small molecule acceptors

153 er the nonfullerene acceptor EH-IDTBR or the fullerene derivative, [6,6]-phenyl C71 butyric acid meth

154 donor-acceptor polyfluorene copolymer and a fullerene derivative.

155 ng of the diffusion and intercalation of the fullerene-derivative within the polymer layer.

156 Importantly, fullerene derivatives 2a-c did not inhibit in vitro PR a

157 fabricated with either [60]PCBM or [70]PCBM fullerene derivatives as acceptor, the efficiency of cha

158 rate dilute conditions (0.03 M) leads to [60]fullerene derivatives as epimeric mixtures ( approximate

159 icancer effects of a series of water-soluble fullerene derivatives bearing amino acid (F1-F7) and thi

160 t to the vast majority of known cytostatics, fullerene derivatives do not show any significant acute

161 Solubilized fullerene derivatives have revolutionized the developmen

162 tion of protein corona on the surface of [60]fullerene derivatives is changing the landscape of their

163 60)) and the formation of highly hydrophilic fullerene derivatives is introduced.

164 Both fullerene derivatives strongly inhibited the tumor growt

165 ion pattern, represent the first examples of fullerene derivatives which combine central, axial, and

166 hilic substitution reactions to generate new fullerene derivatives, which can potentially lead to a w

167 o significantly improved relative to polymer:fullerene devices.

168 separated upon increasing energy offset and fullerene domain density.

169 from consisting of molecularly mixed polymer-fullerene domains to consisting of both molecularly mixe

170 ficient in the high energy offset blend with fullerene domains.

171 to consisting of both molecularly mixed and fullerene domains.

172 t reported for a covalently linked porphyrin-fullerene dyad.

173 t efficient polymer-acceptor alternatives to fullerenes (e.g. PC61 BM or its C71 derivative) are base

174 ate clusters are reminiscent of redox-active fullerenes (e.g., C60(n), where n = +1, 0, -1, -2, -3, -

175 d on Borromean rings, dodecaamine cages, and fullerenes, each of which carrying a defined number of c

176 n to develop replacements; the so-called non-fullerene electron acceptors.

177 er, providing a noncovalent method of tuning fullerene electronics.

178 physical properties of these cages and their fullerene-encapsulated adducts were studied in depth.

179 Fullerene extracts are easily available from fullerene s

180 otifs are utilized as recognition motifs for fullerenes, facilitating novel intermolecular, solvent t

181 uch greater than what could be achieved with fullerene fillers.

182 Fullerene fragments, referred to as buckybowls, are garn

183 ong the best performance so far reported for fullerene-free organic photovoltaics and is inspiring fo

184 e, we exploit strong coupling by embedding a fullerene-free organic solar cell (OSC) photo-active lay

185 Fullerene-free organic solar cells show over 11% power c

186 ture for so long time is rarely reported for fullerene-free OSCs, which might be due to the unique un

187 rativity in binding pairs of anions from the fullerene-free parent: in one case, positive cooperativi

188 egioselectivity in the DA reaction of hollow fullerenes from the usual [6,6] bond to the [5,6] bond i

189 e of electron transfer times from polymer to fullerene, from 240 fs to as short as 37 fs.

190 molecular diodes on the basis of endohedral fullerenes (fullerene switching diode, FSD), encapsulate

191 immature Ty3 particles revealed an irregular fullerene geometry previously described for mature retro

192 ate charge transport through graphene/single-fullerene/graphene hybrid junctions using a single-molec

193 d excited state interactions that occur upon fullerene guest encapsulation characterized by a range o

194 The binding of pairs of fullerene guests was observed to effect the all-or-nothi

195 f this system with respect to the parent C60 fullerene have been analyzed in detail by using the acti

196 Fullerenes have formed an integral part of high performa

197 e unique physical and chemical properties of fullerenes have offered new opportunities to tailor both

198 Applying a thienoisoindigo-COF:fullerene heterojunction as the photoactive component, w

199 The interaction of gas phase endohedral fullerene Ho3N@C80 with intense (0.1-5 x 10(14) W/cm(2))

200 ggregation kinetics of nC60 and higher-order fullerene (HOF) clusters, i.e., nC70, nC76, and nC84, wa

201 atform can present single- or double-tweezer fullerene hosting behavior.

202 bilized by an allylic group cycloadds to [60]fullerene in an efficient manner and with a good diaster

203 )) and thereby improve the solubility of the fullerene in polar solvents (e.g. water).

204 full electron transfer from the Green Box to fullerene in the ground state.

205 s are about as poorly explored as the use of fullerenes in catalysis.

206 f non-IPR (isolated pentagon rule) exohedral fullerenes in contrast with their pristine fullerene cou

207 -isomer, and particularly single-enantiomer, fullerenes in organic electronic materials and devices a

208 dvances in the past year, finally surpassing fullerenes in performance.

209 electronics based on numerous sub-nanoscale fullerenes in the large family of carbon allotropes is a

210 significantly changed the characteristics of fullerene including its particle size and surface charge

211 that the interactions between saccharide and fullerene increase with the increase units of the saccha

212 hat the electron-accepting properties of the fullerenes inside the capsules were altered depending on

213 pockets; an X-ray crystal structure of three fullerenes inside the tetrahedron was obtained.

214 e electronically active sites at the polymer/fullerene interfaces in model bulk-heterojunction blends

215 -in which the central alkyne scaffold of [60]fullerene is connected to 12 sugar-containing [60]fuller

216 nk amino acid and peptide derivatives to [60]fullerene is described.

217 he regioselectivity of chemical additions to fullerenes is a major goal in the field of reactivity of

218 standing the relative stability of exohedral fullerenes is an important aspect of fullerene chemistry

219 tabilization of anionic transition states on fullerenes is shown to accelerate disfavored enolate add

220 t systems for the noncovalent recognition of fullerenes is unprecedented, in part because archetypal

221 heterostructures, including the role of the fullerenes, is addressed to provide an in-depth understa

222 ival or surpass the corresponding values for fullerenes, ITIC-0F, and ITIC-4F, and track a positive c

223 Air-stable doping of the n-type fullerene layer in an n-i-p planar heterojunction perovs

224 namics and enhance the optical response of a fullerene layer, enabling hybrid magneto-molecular optoe

225 lamide functionalised reduced graphene oxide-fullerene layer-by-layer assembled dual imprinted polyme

226 lecular dynamics and optical properties of a fullerene layer.

227 single molecule switch using the endohedral fullerene Li@C(60) that displays 14 molecular states whi

228 allofullerenes, formed by encaging Gd inside fullerenes like C80, can exhibit enhanced proton relaxit

229 e B40 cage cluster unveiled the existence of fullerene-like boron clusters (borospherenes).

230 renes unveiled the capacity of boron to form fullerene-like cage structures.

231 Inorganic nanotubes (NTs) and fullerene-like nanoparticles (NPs) of WS2 were discovere

232 Finally, the various applications of the fullerene-like NPs of WS2 and NTs formed therefrom are d

233 e typical fullerene acceptor with endohedral fullerene Lu3N@PC80BEH.

234 The powerful electron accepting ability of fullerenes makes them ubiquitous components in biomimeti

235 consisting of p-type polymers and n-type non-fullerene materials, which is passivated using nickel fo

236 f 2HPOP and ZnPOP for the enrichment of real fullerene mixtures is also demonstrated.

237 ry is illustrated by considering two polymer:fullerene model systems.

238 The introduction of fullerene moieties dramatically improved the conductivit

239 eptor BHJ blends based on polymer donors and fullerene molecular acceptors.

240 ide functionalised reduced graphene oxide or fullerene molecules, which yielded very inferior sensiti

241 L-Serine imprinted acrylamide functionalized fullerene molecules.

242 ics (OPVs) was produced by integrating C(60) fullerene monomers into ionene polymers.

243 hyperthermia as an adjunctive therapy to [60]fullerene nanoparticle-based drug delivery systems in ta

244 g affinity exceeding 10(8) M(-1) despite the fullerene not fully entering the cavity of the host (X-r

245 ves of phosphangulene can cocrystallize with fullerenes or even bind them in solution.

246 ible approach to the successful oxidation of fullerenes (oxC(60)) and the formation of highly hydroph

247 he retro-hydrophosphination reactions of [60]fullerene/phosphine borane compounds offer a promising n

248 ation of large hydrophobic guests, including fullerenes, polycyclic aromatic hydrocarbons, and steroi

249 quantum dot-sensitized solar cells, polymer-fullerene polymer solar cells, organometal halide perovs

250 solved experimental data obtained on polymer:fullerene, polymer:polymer, and small-molecule blends wi

251 nce of this phenomenon from experiments on a fullerene-porphyrin dyad.

252 his situation has changed recently, with non-fullerene PSCs developing very rapidly.

253 The power conversion efficiencies of non-fullerene PSCs have now reached over 15 %, which is far

254 Among the various non-fullerene PSCs, all-polymer solar cells (APSCs) based on

255 onor polymers known to achieve high FFs with fullerenes, PTPD3T, PBTI3T, and PBTSA3T.

256 ry both the fullerene substitution and donor/fullerene ratio which allow us to control both aggregate

257 fore, the essential molecular details of the fullerene recognition and binding process into the coord

258 In this work, the key steps of fullerene recognition and binding processes have been de

259 the nitrogen atom and the CH fragment in the fullerene reduces the interaction between the deformed r

260 nt insights into the formation of all carbon fullerenes reveal that conditions in charcoal formation

261 the coordination capsule and the origins of fullerene selectivity remain elusive.

262 o determine structures of four classes of CA Fullerene shell assemblies.

263 ide functionalised reduced graphene oxide or fullerene, single layered acrylamide functionalised redu

264 Specifically, non-fullerene small-molecule solar cells have recently shown

265 Toxicity to D. magna was as follows: fullerene soot > multiwall carbon nanotubes > graphene.

266 istic effects of binary mixtures composed of fullerene soot and organic co-contaminants as malathion,

267 s similar to that found in thermally treated fullerene soot indicates that they share a nanostructure

268 Fullerene extracts are easily available from fullerene soot, but finding an efficient strategy to obt

269 the toxicity of three carbon nanomaterials (fullerene-soot, multiwall carbon nanotubes, and graphene

270 The formation of the fullerene-steroid hybrids proceeds with preference for t

271 ion of the most pyramidalized regions of the fullerene structure.

272 en by the strain release of the Gd(3)N@C(80) fullerene structure.

273 We vary both the fullerene substitution and donor/fullerene ratio which a

274 trically and electronically complementary to fullerenes such as C(60) and C(70).

275 Mass spectrometry revealed no magic number fullerenes such as C(60) or C(70) in the charcoal.

276 gineering as exemplified by various pristine fullerenes such as C(60), C(70), C(76) and C(90).

277 iodes on the basis of endohedral fullerenes (fullerene switching diode, FSD), encapsulated with polar

278 S protein effectively lowered the amounts of fullerene taken up by Caco-2 cells, which are derived fr

279 chains featuring pairs of electron accepting fullerenes, that is, C60 and C70.

280 Unlike conventional forms of fullerene, the iconic Buckminsterfullerene cage, I h-C60

281 Unlike in C60, in doped fullerenes, the breaking of the cage spherical symmetry

282 gulene are predisposed to cocrystallize with fullerenes, thereby yielding materials in which metals a

283 sting that the effect of the coordination of fullerene to one face of our supramolecular platform was

284 U(19) adopts an incomplete fullerene topology and was utilized as a precursor from

285 Furthermore, we explore fullerene-type endohedral isomers, i.e., cages with inte

286 Novel actinide cluster fullerenes, U(2)C(2)@I(h)(7)-C(80) and U(2)C(2)@D(3h)(5)

287 In the case of cages loaded with C60 or C70 fullerenes, ultrafast host-to-guest electron transfer wa

288 r use in hydrophosphination reactions of [60]fullerene under phase-transfer catalysis has demonstrate

289 d so far has only been reported for solvated fullerenes under compression. Here, a report on the crea

290 rene is connected to 12 sugar-containing [60]fullerene units (total 120 mannoses)-exhibit an outstand

291 A fullerene variant, Indene-C60 bis-adduct, is used to ach

292 that a supramolecular complex of saccharide-fullerene was formed through CH-pai and/or OH-pai intera

293 The binding of multiple fullerenes was observed to increase the electron affinit

294 , a photochemical desulfinylation of an open fullerene, was completed, even though it is inhibited by

295 ir conductance, and via heteroatom doping of fullerene, which introduces transport resonances and inc

296 nonisolated pentagon rule (IPR) (#6094)C(68) fullerene, which possesses a triplet ground state.

297 renylstyrenes based on the reaction of C(60) fullerene with terminal acetylenes and EtMgBr in the pre

298 on model was in the low micromolar range for fullerenes with 12 and 36 mannoses.

299 study thus provides key strategies to design fullerenes with large chiroptical responses for use as c

300 predict the relative stability of exohedral fullerenes without the need for electronic structure cal