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Journal articles on the topic 'Hexakisadducts'

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Author: Grafiati
Published: 11 March 2023

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1

Kraft, Andreas, Johannes Stangl, Ana-Maria Krause, Klaus Müller-Buschbaum, and Florian Beuerle. "Supramolecular frameworks based on [60]fullerene hexakisadducts." Beilstein Journal of Organic Chemistry 13 (January 2, 2017): 1–9. http://dx.doi.org/10.3762/bjoc.13.1.

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[60]Fullerene hexakisadducts possessing 12 carboxylic acid side chains form crystalline hydrogen-bonding frameworks in the solid state. Depending on the length of the linker between the reactive sites and the malonate units, the distance of the [60]fullerene nodes and thereby the spacing of the frameworks can be controlled and for the most elongated derivative, continuous channels are obtained within the structure. Stability, structural integrity and porosity of the material were investigated by powder X-ray diffraction, thermogravimetry and sorption measurements.
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2

Braun, Martin, Uwe Hartnagel, Elena Ravanelli, Boris Schade, Christoph Böttcher, Otto Vostrowsky, and Andreas Hirsch. "Amphiphilic [5:1]- and [3:3]-Hexakisadducts of C60." European Journal of Organic Chemistry 2004, no. 9 (May 2004): 1983–2001. http://dx.doi.org/10.1002/ejoc.200300663.

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3

Herzog, Andrea, Andreas Hirsch, and Otto Vostrowsky. "Dendritic Mixed Hexakisadducts of C60 with aTh Symmetrical Addition Pattern." European Journal of Organic Chemistry 2000, no. 1 (January 2000): 171–80. http://dx.doi.org/10.1002/(sici)1099-0690(200001)2000:1<171::aid-ejoc171>3.0.co;2-b.

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4

Hörmann, Frank, Michael Brettreich, Wolfgang Donaubauer, Frank Hampel, and Andreas Hirsch. "Highly Efficient Synthesis of Globular (Bola)amphiphilic [5:1]Hexakisadducts of C60." Chemistry - A European Journal 19, no. 8 (January 10, 2013): 2814–25. http://dx.doi.org/10.1002/chem.201203863.

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5

Beuerle, Florian, and Andreas Hirsch. "Synthesis of Amphiphilic [60]Fullerene [3:3]Hexakisadducts with Four Spherically Defined Addend Zones." Chemistry - A European Journal 15, no. 30 (July 27, 2009): 7447–55. http://dx.doi.org/10.1002/chem.200900330.

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6

Hirsch, Andreas, and Otto Vostrowsky. "C60 Hexakisadducts with an Octahedral Addition Pattern − A New Structure Motif in Organic Chemistry." European Journal of Organic Chemistry 2001, no. 5 (March 2001): 829–48. http://dx.doi.org/10.1002/1099-0690(200103)2001:5<829::aid-ejoc829>3.0.co;2-v.

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7

Hartnagel, Uwe, Andreas Hirsch, Delphine Felder-Flesch, Jean-Louis Gallani, and Cyril Bourgogne. "Spreading behaviour of a series of amphiphilic [3 : 3] [60]fullerene hexakisadducts: a systematic study." Journal of Experimental Nanoscience 3, no. 3 (September 2008): 229–44. http://dx.doi.org/10.1080/17458080802294432.

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8

Hirsch, A., and O. Vostrowsky. "ChemInform Abstract: C60 Hexakisadducts with an Octahedral Addition Pattern - A New Structure Motif in Organic Chemistry." ChemInform 33, no. 4 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200204268.

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9

Qian, Wenyuan, and Yves Rubin. "A Parallel Library of all Seven A2+B2+C2Th Regioisomeric Hexakisadducts of Fullerene C60: Inspiration from Werner's Octahedral Stereoisomerism." Angewandte Chemie 112, no. 17 (September 1, 2000): 3263–67. http://dx.doi.org/10.1002/1521-3757(20000901)112:17<3263::aid-ange3263>3.0.co;2-p.

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10

Qian, Wenyuan, and Yves Rubin. "A Parallel Library of all Seven A2+B2+C2Th Regioisomeric Hexakisadducts of Fullerene C60: Inspiration from Werner's Octahedral Stereoisomerism." Angewandte Chemie 39, no. 17 (September 1, 2000): 3133–37. http://dx.doi.org/10.1002/1521-3773(20000901)39:17<3133::aid-anie3133>3.0.co;2-0.

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11

Diekers, Michael, Chuping Luo, Dirk M. Guldi, and Andreas Hirsch. "Th-Symmetrical Hexakisadducts of C60 with a Densely Packed π-Donor Shell Can Act as Energy- or Electron-Transducing Systems." Chemistry - A European Journal 8, no. 4 (February 15, 2002): 979–91. http://dx.doi.org/10.1002/1521-3765(20020215)8:4<979::aid-chem979>3.0.co;2-6.

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12

Schade, Boris, Kai Ludwig, Christoph Böttcher, Uwe Hartnagel, and Andreas Hirsch. "Die supramolekulare Struktur von 5 nm großen sphärischen Micellen mitD3-Symmetrie, selbstorganisiert aus einem amphiphilen [3:3]-Hexakisaddukt von C60." Angewandte Chemie 119, no. 23 (June 4, 2007): 4472–75. http://dx.doi.org/10.1002/ange.200604784.

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13

"[60]Fullerene Hexakisadducts for High-added Value Materials." ECS Meeting Abstracts, 2009. http://dx.doi.org/10.1149/ma2009-01/29/1094.

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14

Braun, Martin, Uwe Hartnagel, Elena Ravanelli, Boris Schade, Christoph Boettcher, Otto Vostrowsky, and Andreas Hirsch. "Amphiphilic [5:1]- and [3:3]-Hexakisadducts of C60." ChemInform 35, no. 31 (August 3, 2004). http://dx.doi.org/10.1002/chin.200431098.

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15

Villada, Juan D., Álvaro Duarte-Ruiz, and Manuel N. Chaur. "Síntesis regioespecífica y estudio electroquímico de dos derivados carboxílicos C60 solubles en agua." Revista de la Academia Colombiana de Ciencias Exactas, Físicas y Naturales, January 18, 2021. http://dx.doi.org/10.18257/raccefyn.1187.

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We report a new methodology for the synthesis of two highly symmetric equatorial malonate hexaadducts of C60 fullerene. The synthetic methodology is based on a series of protection and deprotection steps that allow the preparation of a fullerene [60] functionalized with six symmetrical positioned malonate addends without using complicated and expensive separation techniques (highperformance liquid chromatography, HPLC) or long reaction times. This methodology allowed us to prepare the carboxylic adducts 6 (equatorial octacarboxylic tetraadduct of C60) and 8 (equatorial dodecacarboxylic hexakisadduct of C60). As far as we now, compound 6 has not yet been reported. We also studied the electronic properties of the main compounds by UV-Vis spectroscopy and cyclic voltammetry (CV). The reported fullerene adducts exhibited several reversible reduction processes whose electron transfers are controlled by diffusion.
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