ライフサイエンスコーパス: fullerene

1 ganisms, respectively, on bioavailability of fullerene.

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

3 ical factor that affects bioconcentration of fullerene.

4 o produce a condensed graphitic structure or fullerene.

5 on fillers consisting of graphene flakes and fullerenes.

6 s of metal complexes and metal surfaces with fullerenes.

7 lead towards a useful methodology to purify fullerenes.

8 blends of poly(3-hexylthiophene) (P3HT) and fullerenes.

9 esents a subunit for C70 and of other higher fullerenes.

10 orming simple planar molecules and cage-like fullerenes.

11 er corannulene-based molecular receptors for fullerenes.

12 addition reactions or the making of pristine fullerenes.

13 he interaction between CNTs and encapsulated fullerenes.

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

15 rbon charge-transfer magnet, consisting of a fullerene acceptor and single-walled carbon nanotube don

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

17 Here we present a new non-fullerene acceptor that has been specifically designed t

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

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

20 The use of non-fullerene acceptors in organic photovoltaic (OPV) device

21 It is found that non-fullerene acceptors require adjusted buffer layers with

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

23 meV, most of which probably arises from the fullerene acceptors) are beneficial in minimizing energy

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

25 This bis-fullerene adduct exhibits different cooperativity in bin

26 transition metal complexes and fullerene or fullerene adducts.

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

28 ms driving the reduction of photoactivity in fullerene aggregates and the effects of functionalizatio

29 Photoactive fullerene aggregates had weaker fullerene-fullerene and

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

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

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

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

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

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

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

37 gative correlation with the carbon number in fullerenes and was estimated as 220, 150, 100, and 70 mM

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

39 Carbon-based materials, such as acenes, fullerenes, and graphene nanoribbons, are viewed as the

40 e show that the relative isomer stability of fullerene anions is essentially governed by a few simple

41 atively predicting the relative stability of fullerene anions, allowing a rapid determination of suit

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

43 tion occurs in regions where the polymer and fullerene are molecularly intermixed (such as the co-cry

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

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

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

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

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

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

50 Fullerenes as well as endohedral metallofullerenes are c

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

52 ullerodendrimers and cysteine-functionalized fullerene assemblies.

53 rstanding the ultimate environmental fate of fullerene based materials.

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

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

56 They also rely on fullerene-based acceptors, which themselves have issues

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

58 Fullerene-based gel-nanocomposites show applications in

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

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

61 eto-electroluminescence (MEL) measurement in fullerene-based light emitting diodes (LED).

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

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

64 cells have achieved efficiencies as high as fullerene-based solar cells.

65 ght photoactivity of these materials advance fullerene-based technologies for water treatment.

66 The distribution coefficient (Klipw) of fullerene between solid supported lipid membranes (SSLMs

67 ereo-, and atropselective formation of a C60 fullerene bisadduct racemate from a complex mixture of 1

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

69 a front sub-cell and a low band gap polymer:fullerene blend film as a back cell on planar glass subs

70 nation, and transport characteristics of the fullerene blend films are found to be identical.

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

72 The DARP- and Stille-derived copolymer and fullerene blend microstructural properties and morpholog

73 efficienct a-Si:H and 7.5% efficient polymer:fullerene blend solar cells results in a power conversio

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

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

76 chanisms during charge generation in polymer:fullerene blends exploiting our well-defined understandi

77 es is studied in two closely related polymer-fullerene blends with differing polymer fluorination and

78 In this study, the functionalization of a fullerene building block in a stepwise process by means

79 tween an MoOx anode interlayer and a polymer:fullerene bulk heterojunction is investigated.

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

81 None of the non-fullerene bulk heterojunction solar cells have achieved

82 a solar cell, which is a record high for non-fullerene bulk heterojunctions.

83 s study suggest that surface modification of fullerene by environmentally relevant matrices can signi

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

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

86 Fullerene C60 (FC60), fullerene C70 (FC70), single-walle

87 A porphyrin-fullerene C60 dyad (TCP-C60) substituted by carbazoyl gr

88 with isotactic poly(methyl methacrylate) and fullerene C60 generates supramolecular crystalline helic

89 Fullerene C60 nanoparticles are being used in broad rang

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

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

92 Fullerene C60, co-introduced via an organic solvent, did

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

94 sed cavity suitable for encapsulation of the fullerene C60, whereas original cage 1 forms a unique co

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

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

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

98 Upon treatment with the fullerenes C60 or C70 , this cage was found to transform

99 tions to predict the thermal conductivity of fullerene (C60) and its derivative phenyl-C61-butyric ac

100 ated task and how dedicatedly functionalized fullerene (C60) can perform on this stage is a challenge

101 that have been reported for functionalizing fullerene (C60) derivatives and their application in dif

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

103 Carbon fullerene (C60) has emerged at the forefront of nanoscal

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

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

106 Fullerene C60 (FC60), fullerene C70 (FC70), single-walled carbon nanotubes (SW

107 fective pi-orbital hybridization between the fullerene cage and the aromatic anchor (addend), the aza

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

109 Our calculations show that Sc3N inside the fullerene cage creates a sharp resonance near the Fermi

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

111 ey synthetic step is the closure of the open fullerene cage with the escape of HF minimized.

112 tal arrangement of the trimer, with a single fullerene cage wrapped by four corannulene subunits of t

113 unit inside a previously unseen C(2v)(9)-C86 fullerene cage.

114 pplication in sensor devices has proven that fullerene can be implemented successfully in preparing b

115 of reversible oxidation/reduction, and hence fullerene can work either as an electrophile or nucleoph

116 The solubility of pristine fullerenes can be enhanced by mixing C60 and C70 due to

117 2F]T polymers are particularly promising non-fullerene candidates for "all-polymer" BHJ solar cells.

118 length (10,0) carbon nanotube (CNT) with two fullerene caps, namely D5(450)-C100, is an ideal prototy

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

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

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

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

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

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

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

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

127 the aggregation behavior by stabilizing all fullerene clusters, even at a 100 mM NaCl concentration.

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

129 Comparing a variety of small-molecule donor-fullerene combinations, we illustrate how tuning of mole

130 Fullerenes combined with AOx improved the selectivity to

131 rgy band that appeared in several reports on fullerene complexation with hosts containing the 1,3-dit

132 These fullerene compounds were then reacted with thiol derivat

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

134 mesoporous silica matrix and a nucleus-like fullerene core.

135 tions suggest that the observed nonclassical fullerene could be a kinetically trapped species derived

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

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

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

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

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

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

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

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

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

145 onductivity compared to the pure amphiphilic fullerene derivative.

146 donor-acceptor polyfluorene copolymer and a fullerene derivative.

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

148 Collectively, our studies indicate fullerene derivatives 2a-c as potent and novel HIV-1 mat

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

150 rials, which typically rely on water-soluble fullerene derivatives and elaborate immobilization metho

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

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

153 single-walled carbon nanotubes (SWCNTs) and fullerene derivatives by employing time-resolved microwa

154 The decrease in thermal conductivity of fullerene derivatives can be attributed to the reduction

155 s as electron acceptors that are on par with fullerene derivatives in efficient solar cells.

156 Fullerene derivatives such as [6,6]-phenyl-C61 or 71-but

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

158 e C60 aggregates (nC60) to oxidized, soluble fullerene derivatives, have been described as key proces

159 of alkyl chain on the thermal properties of fullerene derivatives, we perform molecular dynamics (MD

160 lloidal suspensions of C60 and various [C60] fullerene derivatives, yet few have investigated the pho

161 n formed from a binary blend of P3HT and C60 fullerene derivatives.

162 do not improve the morphology of endohedral fullerene devices as expected.

163 o significantly improved relative to polymer:fullerene devices.

164 to the strong interactions between negative fullerene dispersions and positive lipid head groups.

165 The higher Klipw for fullerene distribution to ternary lipid mixture membrane

166 ion through relatively phase-pure polymer or fullerene domains limits the rate of electron and hole t

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

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

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

170 rosslinkable silane-functionalized and doped fullerene electron transport layer, the perovskite devic

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

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

173 The prominent aspects of fullerene explain its outstanding performance in biosens

174 Fullerene extracts are easily available from fullerene s

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

176 e first example of a crystalline metal-donor-fullerene framework, in which control of the donor-fulle

177 Design principles for fullerene-free acceptors remain unclear in the field.

178 Fullerene-free and processing additive-free 8.5% efficie

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

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

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

182 e achieved which is the highest reported for fullerene-free P3HT devices.

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

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

185 Photoactive fullerene aggregates had weaker fullerene-fullerene and fullerene-O2 interactions, sugge

186 The state-of-the-art research on fullerene functionalization and its application in senso

187 worldwide to invent a variety of methods of fullerene functionalization with a purpose of incorporat

188 Fullerene groups occupy periodic lattice sites, sandwich

189 ween the porphyrin units of the host and the fullerene guest bound within its central cavity.

190 ts, and the latest strategies to release the fullerene guest will be described.

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

192 C38H14-buckybowl, a fragment bowl of the C70 fullerene, has been studied with scanning tunneling micr

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

194 he excellent photophysical properties of C60 fullerenes have spurred much research on their applicati

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

196 ing molecular surgery to give the endohedral fullerene HF@C60.

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

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

199 controlled and versatile strategy to design fullerene hosts, and the latest strategies to release th

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

201 ce in biosensing devices as a mediator, e.g. fullerene in organic solvents exhibits five stages of re

202 r cells is also possible by the inclusion of fullerene in single-walled carbon nanotubes (SWCNTs) kno

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

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

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

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

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

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

209 termixed (such as the co-crystal phase where fullerenes intercalate between polymer chains in pBTTT:P

210 Gaining insight into the detailed fullerene intercalation mechanism is important for the d

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

212 ionalization methods include modification of fullerene into water soluble derivatives and conjugation

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

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

215 Fullerene is stable and its spherical structure produces

216 sm by which carbon condenses to form PAHs or fullerenes is a problem that has garnered considerable t

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

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

219 A crosslinked silane-modified fullerene layer also enhances the water and moisture sta

220 Methylammonium iodide is introduced in the fullerene layer for n-doping via anion-induced electron

221 groups are bonded onto fullerene to make the fullerene layer highly water-resistant.

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

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

224 lecular dynamics and optical properties of a fullerene layer.

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

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

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

228 sing numerous randomly distributed nanosized fullerene-like spheroids.

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

230 es commonly pursued to create such supported-fullerene materials, which typically rely on water-solub

231 )(0)- and C(6)(0)-derivative-based supported fullerene materials.

232 at the lipid-water distribution mechanism of fullerene may be different from that of molecular level

233 Employing fullerene-metal matrix for the detection of tumor and ca

234 The reactions of the open-cage fullerene, MMK-9, with an open 12-membered ring on its s

235 roach prevents the aggregation of individual fullerene molecules in water, thus allowing fullerene to

236 e findings suggest a new means of organizing fullerene molecules into a rich variety of lattices to g

237 e order, and, as a result, it does not allow fullerene molecules to intercalate between the polymer s

238 Annealed at the high temperature, the fullerene molecules were selectively sublimated from the

239 renes with water, oxygen, and/or neighboring fullerene molecules, complimented by physical and chemic

240 ene framework, in which control of the donor-fullerene mutual orientation was achieved through chemic

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

242 Fullerene nanostructures are well known for their unique

243 The thermal stability of fullerene nanostructures, such as their sublimation at h

244 In this work, We observed fullerene nanowhiskers (FNWs) in situ with scanning heli

245 ggregates had weaker fullerene-fullerene and fullerene-O2 interactions, suggesting the importance of

246 ns of various transition metal complexes and fullerene or fullerene adducts.

247 effect in planar heterojunction cyanine dye/fullerene organic solar cells enables one to directly mo

248 rolling the nanoscale arrangement in polymer-fullerene organic solar cells is of paramount importance

249 re even higher than reported values for [70]-fullerene:PBDTTT-CT solar cells.

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

251 High efficiency polymer:fullerene photovoltaic device layers self-assemble with

252 emonstration of efficient, stable perovskite/fullerene planar heterojunction solar cells.

253 Grafting of the fullerene platform with a variety of azido derivatives,

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

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

256 t guidance to improve the performance of non-fullerene polymer solar cells.

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

258 ysical and chemical characterizations of the fullerenes pre- and postaggregation.

259 To within statistical error, spherical fullerenes provide a nearly size-independent level of re

260 The cavity inside fullerenes provides a unique environment for the study o

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

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

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

264 on, and characterization of a new endohedral fullerene, Sc2C88, is reported.

265 single-molecule junctions of the endohedral fullerene Sc3N@C80 connected to gold electrodes using a

266 evere deformations than conventional polymer-fullerene solar cells, making them much better candidate

267 2-pyridyl diketopyrrolopyrrole (DPP) polymer-fullerene solar cells.

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

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

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

271 . magna exposed to mixtures of malathion and fullerene soot.

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

273 ated the photochemistry of other larger cage fullerene species (e.g., C70, C74, C84, etc.) in water.

274 and the excited state dynamics of aggregate fullerene species via transient absorption spectroscopy.

275 These one-dimensional arrays of fullerenes stack along the long axis of needle-like sing

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

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

278 ixtures are processable in methanol and show fullerene-templated crystalline structures in spin-cast

279 ns of the flexible spacer wrapped around the fullerene that brings the C60 in pi-pi overlap with the

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

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

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

283 ydrophobic functional groups are bonded onto fullerene to make the fullerene layer highly water-resis

284 fullerene molecules in water, thus allowing fullerene to retain its photoactivity, yet is much less

285 60-) (U60), an actinide polyoxometalate with fullerene topology, can be induced by the addition of mo

286 ed CuBr framework, which does not follow the fullerene topology.

287 It is concluded that the novel 3DP fullerene-type bio-carriers are ideal carriers for biofi

288 polyarenes, have also been found to exhibit "fullerene-type chemistry" at their interior carbon atoms

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

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

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

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

293 Klipw of fullerene was significantly higher with a cationic lipid

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

295 ly different photoactivities exhibit similar fullerene-water interactions as well as surface and aggr

296 has a lower electron affinity than standard fullerenes, which can raise the open circuit voltage of

297 hoto-oxygenation and ring opening to yield a fullerene with a hole in the cage.

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

299 molecular interactions in systems containing fullerenes with water, oxygen, and/or neighboring fuller

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