Tổng hợp và phân tích nhiệt trọng lượng của các phức hợp bổ sung của các ligand đại phân tử aza-crown cho nhóm cho O2N2 với [60]fullerene

Taylor R, Walton DRM. The chemistry of fullerenes. Nature (London). 1993;363:685–93. Diederich F, Thilgen C. Covalent fullerene chemistry. Science. 1996;27:317–24. Guldi DM, Zilbermann I, Anderson G, Kotov NA, Tagmatarchise N, Prato M. Nanosized inorganic/organic composites for solar energy conversion. J Mat Chem. 2005;15:114–8. Spanig F, Ruppert M, Dannhauser J, Hirsch A, Guldi DM. trans-2 addition pattern to power charge transfer in dendronized metalloporphyrin C60 conjugates. J Am Chem Soc. 2009;131:9378–88. Villegas C, Krokos E, Bouit PA, Delgado JL, Guldi DM, Martin N. Efficient light harvesting anionic heptamethine cyanine–[60] and [70]fullerene Hybrids. Energy Environ Sci. 2011;4:679–84. Perez EM, Martin N. Curves ahead: molecular receptors for fullerenes based on concave–convex complementarity. Chem Soc Rev. 2008;37:1512–9. Wu Z-Q, Shao X-B, Li C, Hou J-L, Wang K, Jiang X-K, Li Z-T. Hydrogen-bonding-driven preorganized Zinc porphyrin receptors for efficient complexation of C60, C70, and C60 derivatives. J Am Chem Soc. 2005;127:17460–8. Klaerner FG, Kahlert B. Molecular tweezers and clips as synthetic receptors. molecular recognition and dynamics in receptor − substrate complexes. Acc Chem Res. 2003;36:919–32. Tucci FC, Rudkevich DM, Rebek J Jr. Deeper cavitands. J Org Chem. 1999;64:4555–9. Atwood JL, Koutsantonis GA, Raston CL. Purification of C60 and C70 by selective complexation with calixarenes. Nature. 1994;368:229–31. Suzuki T, Nakashima K, Shinkai S. Very Convenient and Efficient Purification Method for Fullerene (C60) with 5,11,17,23,29,35,41,47-Octa-tert-butylcalix[8]arene-49,50,51,52,53,54,55,56-octol. Chem Lett. 1994;23:699–702. Hardie MJ, Raston CL. Confinement and recognition of icosahedral main group cage molecules: fullerene C60 and o-, m-, p-dicarbadodecaborane(12). Chem Commun. 1999;. doi:10.1039/A900787C. Murthy CN, Geckeler KE. The water-soluble β-cyclodextrin–[60]fullerene complex. Chem Commun. 2001;13:1194–5. Sun D, Tham FS, Reed CA, Chaker L, Boyd PDW. Supramolecular fullerene–porphyrin chemistry. fullerene complexation by metalated “jaws porphyrin” hosts. J Am Chem Soc. 2002;12:6604–12. Milliken J, Keller TM, Raronavski AP, McElvany SW, Callahan JH, Nelson HH. Thermal and oxidative analyses of buckminsterfullerene. Chem Mater. 1991;3:386–7. McKee DW. The thermal stability of fullerene in air. Carbon. 1991;29:1057–8. Janaki J, Premila M, Gopalan P, Sastry VS, Sundar CS. Thermal stability of a fullerene-amine adduct. Thermochim Acta. 2000;356:109–16. Zhao L, Guo Z, Ran S, Cao Z, Fang Z. The effect of fullerene on the resistance to thermal degradation of polymers with different degradation processes. J Therm Anal Calorim. 2014;115:1235–44. Zhao L, Cao Z, Fang Z, Guo Z. Influence of fullerene on the kinetics of thermal and thermo-oxidative degradation of high-density polyethylene by capturing free radicals. J Therm Anal Calorim. 2013;. doi:10.1007/s10973-013-3158-4. Lima AMF, Musumeci AW, Liu H-W, Waclawik ER. Silva GG. Purity evaluation and influence of carbon nanotube on carbon nanotube/graphite thermal stability. J Therm Anal Calorim. 2009;97:257–63. Han X, Sun YL, Wang TF, Lin ZK, Li SF, Zhao FQ, Liu ZR, Yi JH, Ren XN. Thermal decomposition of ammonium perchlorate based mixture with fullerenes. J Therm Anal Calorim. 2008;91:551–7. Goswami TH, Singh R, Alam S, Mathur GN. Thermal analysis: a unique method to estimate the number of substituents in fullerene derivatives. Thermochim Acta. 2004;419:97–104. Basiuk EV (Golovataya-Dzhymbeeva), Basiuk VA, Shabelnikov VP, Golovatyi VG, Flores JO, Saniger JM, et al. Reaction of silica-supported fullerene C60 with nonylamine Vapor. Carbon. 2003;41:2339–2346. Ghanbari B, Alishah Aratboni M. Thermodynamic study on the effect of O2N2-aza-crown macrocyclic ring-size in complexation with [60]fullerene. Fuller, Nanotub Carbon Nanostructures. 2013;21:394–402. Armstrong LG, Grimsley PG, Lindoy LF, Lip HC, Norris VA, Smith RJ. Studies involving nitrogen–oxygen-donor macrocyclic ligands. 4. Interaction of nickel(II) with new 14- and 17-membered crown macrocycles. Inorg Chem. 1978;17:2350–2. Grimsley PG, Lindoy LF, Lip HC, Smith RJ, Baker JT. Synthesis of new 14-,15- and 16-membered crown compounds containing oxygen and nitrogen heteroatoms. Aust J Chem. 1977;30:2095–8. Zarzycki PK, Ohta H, Saito Y, Jinno K. Chromatographic behavior of C60 and C70 fullerenes at subambient temperature with n-alkanes mobile phases. Chromatographia. 2006;64:79–82. Rondeau D, Kreher D, Cariou M, Hudhomme P, Gorgues A, Richomme P. Electrolytic electrospray ionization mass spectrometry of C60-TTF- C60 derivatives: high-resolution mass measurement and molecular ion gas-phase reactivity. Rapid Commun Mass Spectrom. 2001;15:1708–12. Deng J-P, Mou Ch-Y, Han Ch-Ch. C180O2, a V-shaped fullerene trimer. Chem Phys Let. 1996;256:96–100. Saxby JD, Chatfield SP, Palmisano AJ, Vassallo AM, Wilson MA, Pang LSK. Thermogravimetric analysis of buckminsterfullerene and related materials in air. J Phys Chem. 1992;96:17–8.