1994
DOI: 10.1021/cm00044a033
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Nanocrystalline Domains of a Monoclinic Modification of Benzene Stabilized in a Crystalline Matrix of C60

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Cited by 43 publications
(36 citation statements)
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“…For example, C 60 shows maximum solubility in benzene at about 313 K. Crystallization from benzene solution at temperatures below maximum results in formation of triclinic solid solvate with four benzene molecules C 60 Á 4C 6 H 6 which is unstable in air [35,36,45]. The preparation and characterization of solvated fullerenes have been widely studied [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45]. Many fullerene solvates have been observed and make this group of materials an important class of fullerenes.…”
Section: Solvated Fullerenesmentioning
confidence: 99%
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“…For example, C 60 shows maximum solubility in benzene at about 313 K. Crystallization from benzene solution at temperatures below maximum results in formation of triclinic solid solvate with four benzene molecules C 60 Á 4C 6 H 6 which is unstable in air [35,36,45]. The preparation and characterization of solvated fullerenes have been widely studied [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45]. Many fullerene solvates have been observed and make this group of materials an important class of fullerenes.…”
Section: Solvated Fullerenesmentioning
confidence: 99%
“…The fact that fullerenes can generate solvates when they crystallize from solvents is of particular interest [26][27][28][29]. Many studies have focused on the growth and characterization of solvated fullerenes [26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45]. High-pressure studies on this kind of fullerene materials have been carried out by several groups [46][47][48][49][50][51][52][53][54][55][56][57].…”
Section: Introductionmentioning
confidence: 99%
“…It has also been demonstrated that crystallization of C 60 molecules from organic solvents yields C 60 nanocrystals with varied shapes and structures, and that these shapes and structures are dependent upon the crystallization conditions and the solvent(s) employed [23,24,25]. One example is the preparation of C 60 nanowhiskers with a claimed facecentered cubic structure using a liquid-liquid interface method [26].…”
Section: Introductionmentioning
confidence: 99%
“…Among these methods, the solventassisted method is reported to be a convenient and efficient method, which has become widely used for the synthesis of fullerene crystals. Early work reported the synthesis of large-size C 60 crystals (a few hundred micrometers in size) by using dichloromethane [7], 1,1,1-trichloroethane [8], benzene [9], etc., as solvents. Recent studies focused on the synthesis of fullerene crystals with sizes in the submicro/nanometer range, such as nanosheets, nanowhiskers, nanotubes and nanorods [2,3,[5][6][7].…”
Section: Introductionmentioning
confidence: 99%