Literatura académica sobre el tema "Iminofullerene"

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Artículos de revistas sobre el tema "Iminofullerene"

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Clarke, David J., Janis G. Matisons, George P. Simon, Marek Samoc y Anna Samoc. "Polyhedral oligomeric silsesquioxane-bound iminofullerene". Applied Organometallic Chemistry 24, n.º 3 (marzo de 2010): 184–88. http://dx.doi.org/10.1002/aoc.1568.

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Chen, Chen, Yi-Zhou Zhu, Hai-Ying Zhao y Jian-Yu Zheng. "Syntheses of N-bridged ferrocene/porphyrin-fullerene dyads and influence of iminofullerene isomers on the attached chromophores". Tetrahedron Letters 54, n.º 12 (marzo de 2013): 1607–11. http://dx.doi.org/10.1016/j.tetlet.2013.01.061.

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Park, Sung Heum, Changduk Yang, Sarah Cowan, Jae Kwan Lee, Fred Wudl, Kwanghee Lee y Alan J. Heeger. "Isomeric iminofullerenes as acceptors in bulk heterojunction organic solar cells". Journal of Materials Chemistry 19, n.º 31 (2009): 5624. http://dx.doi.org/10.1039/b904535j.

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Liu, Yanjie, Tingting Wang, Jiahui Cao, Zhenfeng Zang, Qingnan Wu, Hezhong Wang, Fuju Tai y Rui He. "Quaternary Ammonium Salts of Iminofullerenes: Fabrication and Effect on Seed Germination". Journal of Agricultural and Food Chemistry 67, n.º 49 (14 de noviembre de 2019): 13509–17. http://dx.doi.org/10.1021/acs.jafc.9b04783.

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Wang, Tingting, Zhenfeng Zang, Shuai Wang, Yuke Liu, Hezhong Wang, Wei Wang, Xiuli Hu, Jinhua Sun, Fuju Tai y Rui He. "Quaternary ammonium iminofullerenes promote root growth and osmotic-stress tolerance in maize via ROS neutralization and improved energy status". Plant Physiology and Biochemistry 164 (julio de 2021): 122–31. http://dx.doi.org/10.1016/j.plaphy.2021.04.019.

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Tesis sobre el tema "Iminofullerene"

1

Clarke, David John y d. clarke@irl cri nz. "The Synthesis and Characterisation of Polyhedral Oligomeric Silsesquioxane Bound Chromophores". Flinders University. School of Chemistry, Physics and Earth Sciences, 2008. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20080908.074728.

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Resumen
This research involved the synthesis and characterisation of a range of optically active polyhedral oligomeric silsesquioxane (POSS) compounds. POSS precursor compounds containing functional groups required for subsequent attachment of the desired functional groups have been synthesised. Examples of such precursor compounds include mono-functionalised POSS compounds with periphery aldehyde, azide, amino and pyridyl functional groups. A variety of POSS compounds, functionalised with a range of optical functionalities, including optical limiters such as fulleropyrrolidine and iminofullerene, and dyes and pigments, including naphthalene, biphenyl, perylene, pyrene and porphyrin have been synthesised. The reaction of mono-functionalised POSS aldehydes with fullerene (C60) in the presence of N-methylglycine yielded the desired POSS fulleropyrrolidines, whilst reaction of mono-functionalised POSS azide with C60 yielded POSS iminofullerenes. All POSS fullerene compounds were characterised by power limiting measurements, exhibiting comparable power limiting to that of parent C60. The microwave condensation of mono-amino POSS with a range of mono- and bis-anhydrides yielded the POSS imide compounds, which were characterised by UV-Vis and fluorescence spectrophotometry. The perylene POSS imide derivative was further characterised by single crystal x-ray crystallography. The naphtha and biphenyl POSS imides exhibited extremely weak fluorescence, whilst the perylene ii POSS imide displayed particularly strong fluorescence, with a quantum yield approaching unity. The incorporation of a pyridyl group on the periphery of a mono-functionalised POSS cage allowed for the synthesis of the first porphyrin functionalised POSS compound. Mono-porphyrin POSS exhibited comparable absorption properties to other pyridyl ligated ruthenium porphyrins. Mono-functionalised pyrene POSS compounds were prepared through the reaction of 1-pyrene acid chloride with mono(3-aminopropyl)POSS. This synthetic pathway offered a convenient route to mono-functionalised pyrene POSS, in preference to the multi-substitution associated with Heck coupling. Mono-pyrene POSS was determined to be strongly fluorescent, exhibiting a high quantum yield of fluorescence
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