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Статті в журналах з теми "Bisadducts"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Bisadducts.

Автор: Grafiati

Опубліковано: 11 березня 2023

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1

Xiao, Zuo, Xinjian Geng, Dan He, Xue Jia, and Liming Ding. "Development of isomer-free fullerene bisadducts for efficient polymer solar cells." Energy & Environmental Science 9, no. 6 (2016): 2114–21. http://dx.doi.org/10.1039/c6ee01026a.

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2

Almeida, José, António Aguiar, Andreia Leite, André M. N. Silva, Luís Cunha-Silva, Baltazar de Castro, Maria Rangel, Giampaolo Barone, Augusto C. Tomé, and Ana M. G. Silva. "1,3-Dipolar cycloadditions with meso-tetraarylchlorins – site selectivity and mixed bisadducts." Organic Chemistry Frontiers 4, no. 4 (2017): 534–44. http://dx.doi.org/10.1039/c6qo00771f.

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3

Sakakibara, Keita, Araki Wakiuchi, Yasujiro Murata, and Yoshinobu Tsujii. "Precise synthesis of double-armed polymers with fullerene C60 at the junction for controlled architecture." Polymer Chemistry 11, no. 27 (2020): 4417–25. http://dx.doi.org/10.1039/d0py00458h.

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4

Si, Weili, Shirong Lu, Naoki Asao, Ming Bao, Yoshinori Yamamoto, and Tienan Jin. "NBS-promoted oxidation of fullerene monoradicals leading to regioselective 1,4-difunctional fullerenes." Chem. Commun. 50, no. 99 (2014): 15730–32. http://dx.doi.org/10.1039/c4cc07780f.

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5

Si, Weili, Xuan Zhang, Naoki Asao, Yoshinori Yamamoto, and Tienan Jin. "Ni-Catalyzed direct 1,4-difunctionalization of [60]fullerene with benzyl bromides." Chemical Communications 51, no. 29 (2015): 6392–94. http://dx.doi.org/10.1039/c5cc01534k.

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6

Li, Fei, Yanbo Shang, Chuang Niu, Chao Li, Xinmin Huang, Guoyong Xu, Jun Xuan, Hongping Zhou, and Shangfeng Yang. "Potassium salt promoted regioselective three-component coupling synthesis of 1,4-asymmetrical [60]fullerene bisadducts with superior electron transport properties." Chemical Communications 56, no. 66 (2020): 9513–16. http://dx.doi.org/10.1039/d0cc03857a.

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Анотація:

An efficient one-pot three-component domino coupling reaction of phenols, C₆₀, and bromoalkanes was developed, resulting in the highly regioselective synthesis of 1,4-asymmetrical C₆₀ bisadducts.

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7

Campidelli, Stéphane, Ester Vázquez, Dragana Milic, Julie Lenoble, Carmen Atienza Castellanos, Ginka Sarova, Dirk M. Guldi, Robert Deschenaux, and Maurizio Prato. "Liquid-Crystalline Bisadducts of [60]Fullerene." Journal of Organic Chemistry 71, no. 20 (September 2006): 7603–10. http://dx.doi.org/10.1021/jo0609576.

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8

Li, Zong-Jun, Sisi Wang, Shu-Hui Li, Tao Sun, Wei-Wei Yang, Kazutaka Shoyama, Takafumi Nakagawa, et al. "Regiocontrolled Electrosynthesis of [60]Fullerene Bisadducts: Photovoltaic Performance and Crystal Structures of C60 o-Quinodimethane Bisadducts." Journal of Organic Chemistry 82, no. 16 (July 31, 2017): 8676–85. http://dx.doi.org/10.1021/acs.joc.7b01732.

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9

Zhang, Bolong, Jonathan M. White, David J. Jones, and Wallace W. H. Wong. "Regioselective synthesis of fullerene multiadducts via tether-directed 1,3-dipolar cycloaddition." Organic & Biomolecular Chemistry 13, no. 42 (2015): 10505–10. http://dx.doi.org/10.1039/c5ob01630d.

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Анотація:

A class of fullerene bisadducts was synthesized in one-pot over two steps with regioselectivity using tether-directed functionalization approach. In extending this class of materials, interesting variations in regioselectivity was observed when different amino acid reactants were used.

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10

Chronakis, Nikos. "The journey of l-tartaric acid in the world of enantiomerically pure bis- and trisadducts of C60 with the inherently chiral trans-3 and all-trans-3 addition patterns." Org. Biomol. Chem. 12, no. 43 (2014): 8574–79. http://dx.doi.org/10.1039/c4ob01666a.

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Анотація:

The journey of l-tartaric acid through its derivative (−)-dimethyl-2,3-O-isopropylidene-l-tartrate in the synthesis of enantiomerically pure diols, cyclo-[n]-malonates and finally, inherently chiral trans-3 bisadducts and all-trans-3 trisadducts of C₆₀ is presented.

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11

Zhou, Zhiguo, David I. Schuster, and Stephen R. Wilson. "Tether-Directed Selective Synthesis of Fulleropyrrolidine Bisadducts." Journal of Organic Chemistry 71, no. 4 (February 2006): 1545–51. http://dx.doi.org/10.1021/jo052213i.

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12

ETTORRE, R., D. MARTON, U. RUSSO, and P. ZANONATO. "Complexes of phthalocyaninatoiron(II) with diazoles." Journal of Porphyrins and Phthalocyanines 05, no. 06 (June 2001): 545–47. http://dx.doi.org/10.1002/jpp.356.

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Анотація:

The complexes of formula [ Fe ( Pc )( diazole )2]·n H 2 O ( Pc = phthalocyaninato dianion ; diazole = pyrazole , 3(5)-methylpyrazole, indazole and 1-phenylimidazole) have been prepared and characterized. The Mössbauer spectra of the bisadducts of [ Fe ( Pc )] with diazoles show values of isomer shift close to those of the corresponding complexes with pyridines, but somewhat smaller values of quadrupole splitting.

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13

Dehmlow, Eckehard V., and Arthur Sleegers. "Notiz über Mono- und Bisaddukte von Diketen an (–)-Menthon / Note on Mono- and Bisadducts of Diketene to (–)-Menthone." Zeitschrift für Naturforschung B 43, no. 7 (July 1, 1988): 921–22. http://dx.doi.org/10.1515/znb-1988-0721.

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Abstract 1,3-Dioxin-4-ones from Ketones Onium salt and acid catalyzed addition of di-ketene to (-)-menthone gives improved yields of 2 and 3. Excess of diketene leads to diastereomeric mixtures of compounds 4 and 6 from menthone and menthol, respectively.

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14

Kordatos, Konstantinos, Susanna Bosi, Tatiana Da Ros, Alfonso Zambon, Vittorio Lucchini, and Maurizio Prato. "Isolation and Characterization of All Eight Bisadducts of Fulleropyrrolidine Derivatives." Journal of Organic Chemistry 66, no. 8 (April 2001): 2802–8. http://dx.doi.org/10.1021/jo001708z.

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15

Zoleo, Alfonso, Anna Lisa Maniero, Marco Bellinazzi, Maurizio Prato, Tatiana Da Ros, Louis Claude Brunel, and Marina Brustolon. "Radical anions of fullerene bisadducts: a multifrequency CW-EPR study." Journal of Magnetic Resonance 159, no. 2 (December 2002): 226–36. http://dx.doi.org/10.1016/s1090-7807(02)00032-0.

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16

Ishi-i, Tsutomu, and Seiji Shinkai. "Synthesis of chiral [60]fullerene-steroid bisadducts using steroid templates." Tetrahedron 55, no. 43 (October 1999): 12515–30. http://dx.doi.org/10.1016/s0040-4020(99)00742-5.

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17

Nenajdenko, V. G., A. M. Moiseev, and E. S. Balenkova. "Reactions of acceptor thiophene 1,1-dioxides with dienes. Synthesis of bisadducts." Russian Chemical Bulletin 54, no. 9 (September 2005): 2182–86. http://dx.doi.org/10.1007/s11172-006-0094-5.

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18

Zhou, Shuiqin, Jianying Ouyang, Patricia Golas, Feng Wang, and Yi Pan. "Structural Study of the Self-Assembled Fullerene Carboxylates: Monoadducts versus Bisadducts." Journal of Physical Chemistry B 109, no. 42 (October 2005): 19741–47. http://dx.doi.org/10.1021/jp053978x.

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19

Nakamura, Yosuke, Masumi Taki, Seiji Tobita, Haruo Shizuka, Hajime Yokoi, Katsuya Ishiguro, Yasuhiko Sawaki, and Jun Nishimura. "Photophysical properties of various regioisomers of [60]fullerene-o-quinodimethane bisadducts." Journal of the Chemical Society, Perkin Transactions 2, no. 1 (1999): 127–30. http://dx.doi.org/10.1039/a803891k.

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20

Figueira-Duarte, Teresa M., Aline Gégout, Jean Olivier, François Cardinali, and Jean-François Nierengarten. "Bismalonates Constructed on a Hexaphenylbenzene Scaffold for the Synthesis ofEquatorialFullerene Bisadducts." European Journal of Organic Chemistry 2009, no. 23 (August 2009): 3879–84. http://dx.doi.org/10.1002/ejoc.200900290.

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21

Chiappara, Clara, Vincenzo Campisciano, Giuseppe Arrabito, Vito Errico, Giovanni Saggio, Gianpiero Buscarino, Michelangelo Scopelliti, Michelangelo Gruttadauria, Francesco Giacalone, and Bruno Pignataro. "Bending Sensors Based on Thin Films of Semitransparent Bithiophene‐Fulleropyrrolidine Bisadducts." ChemPlusChem 85, no. 11 (October 6, 2020): 2455–64. http://dx.doi.org/10.1002/cplu.202000526.

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22

Meng, Xiangyue, Wenqing Zhang, Zhan'ao Tan, Chun Du, Cuihong Li, Zhishan Bo, Yongfang Li, et al. "Dihydronaphthyl-based [60]fullerene bisadducts for efficient and stable polymer solar cells." Chem. Commun. 48, no. 3 (2012): 425–27. http://dx.doi.org/10.1039/c1cc15508c.

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23

Nakamura, Yosuke, Nobutoshi Takano, Tatsuya Nishimura, Eiji Yashima, Mitsuo Sato, Takako Kudo, and Jun Nishimura. "First Isolation and Characterization of Eight Regioisomers for [60]Fullerene−Benzyne Bisadducts." Organic Letters 3, no. 8 (April 2001): 1193–96. http://dx.doi.org/10.1021/ol0156547.

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24

Bottari, Giovanni, Olga Trukhina, Axel Kahnt, Michael Frunzi, Yasujiro Murata, Antonio Rodríguez-Fortea, Josep M. Poblet, Dirk M. Guldi, and Tomás Torres. "Regio-, Stereo-, and Atropselective Synthesis of C60Fullerene Bisadducts by Supramolecular-Directed Functionalization." Angewandte Chemie International Edition 55, no. 37 (May 9, 2016): 11020–25. http://dx.doi.org/10.1002/anie.201602713.

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25

Bottari, Giovanni, Olga Trukhina, Axel Kahnt, Michael Frunzi, Yasujiro Murata, Antonio Rodríguez-Fortea, Josep M. Poblet, Dirk M. Guldi, and Tomás Torres. "Regio-, Stereo-, and Atropselective Synthesis of C60Fullerene Bisadducts by Supramolecular-Directed Functionalization." Angewandte Chemie 128, no. 37 (May 9, 2016): 11186–91. http://dx.doi.org/10.1002/ange.201602713.

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26

Albini, Franca Marinone, Rita De Franco, Tiziano Bandiera, Pierluigi Caramella, Antonino Corsaro, and Giancarlo Perrini. "Crossed bisadducts in the reaction of pyridine with two different nitrile oxides." Journal of Heterocyclic Chemistry 26, no. 3 (May 1989): 757–61. http://dx.doi.org/10.1002/jhet.5570260346.

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27

Huang, Liyi, Min Wang, Tianhong Dai, Felipe F. Sperandio, Ying-Ying Huang, Yi Xuan, Long Y. Chiang, and Michael R. Hamblin. "Antimicrobial photodynamic therapy with decacationic monoadducts and bisadducts of [70]fullerene:in vitroandin vivostudies." Nanomedicine 9, no. 2 (February 2014): 253–66. http://dx.doi.org/10.2217/nnm.13.22.

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28

Polimeno, Antonino, Mirco Zerbetto, Lorenzo Franco, Michele Maggini, and Carlo Corvaja. "Stochastic Modeling of CW-ESR Spectroscopy of [60]Fulleropyrrolidine Bisadducts with Nitroxide Probes." Journal of the American Chemical Society 128, no. 14 (April 2006): 4734–41. http://dx.doi.org/10.1021/ja057414i.

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29

Nishimura, Tatsuya, Kayo Tsuchiya, Sousuke Ohsawa, Katsuhiro Maeda, Eiji Yashima, Yosuke Nakamura, and Jun Nishimura. "Macromolecular Helicity Induction on a Poly(phenylacetylene) withC2-Symmetric Chiral [60]Fullerene-Bisadducts." Journal of the American Chemical Society 126, no. 37 (September 2004): 11711–17. http://dx.doi.org/10.1021/ja046633l.

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30

Chen, Wangqiao, Qian Zhang, Teddy Salim, Sandy Adhitia Ekahana, Xiangjian Wan, Tze Chien Sum, Yeng Ming Lam, Alfred Hon Huan Cheng, Yongsheng Chen, and Qichun Zhang. "Synthesis and photovoltaic properties of novel C60 bisadducts based on benzo[2,1,3]-thiadiazole." Tetrahedron 70, no. 36 (September 2014): 6217–21. http://dx.doi.org/10.1016/j.tet.2014.01.026.

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31

Liu, Chao, Shengqiang Xiao, Xiangping Shu, Yongjun Li, Liang Xu, Taifeng Liu, Yanwen Yu, Liang Zhang, Huibiao Liu, and Yuliang Li. "Synthesis and Photovoltaic Properties of Novel Monoadducts and Bisadducts Based on Amide Methanofullerene." ACS Applied Materials & Interfaces 4, no. 2 (January 20, 2012): 1065–71. http://dx.doi.org/10.1021/am2016975.

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32

Nierengarten, Jean-François, Corinne Schall, Jean-François Nicoud, Benoît Heinrich, and Daniel Guillon. "Amphiphilic cyclic fullerene bisadducts: Synthesis and Langmuir films at the air-water interface." Tetrahedron Letters 39, no. 32 (August 1998): 5747–50. http://dx.doi.org/10.1016/s0040-4039(98)01134-4.

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33

Nakamura, Yosuke, Kyoji O-kawa, Minako Matsumoto, and Jun Nishimura. "Separation and Characterization of [60]Fullerene Bisadducts Modified by 4,5-Dimethoxy- o -quinodimethane." Tetrahedron 56, no. 30 (July 2000): 5429–34. http://dx.doi.org/10.1016/s0040-4020(00)00451-8.

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34

Nakamura, Yosuke, Kyoji O-kawa, Tatsuya Nishimura, Eiji Yashima, and Jun Nishimura. "Systematic Enantiomeric Separation of [60]Fullerene Bisadducts Possessing an Inherent Chiral Addition Pattern." Journal of Organic Chemistry 68, no. 8 (April 2003): 3251–57. http://dx.doi.org/10.1021/jo026657f.

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35

Morvillo, Pasquale, and Eugenia Bobeico. "Bisadducts of C70as Electron Acceptors for Bulk Heterojunction Solar Cells: A Theoretical Study." Fullerenes, Nanotubes and Carbon Nanostructures 19, no. 5 (April 19, 2011): 410–20. http://dx.doi.org/10.1080/15363831003721880.

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36

López, Alejandro Montellano, Francesco Scarel, Noelia Rubio Carrero, Ester Vázquez, Aurelio Mateo-Alonso, Tatiana Da Ros, and Maurizio Prato. "Synthesis and Characterization of Highly Water-Soluble Dendrofulleropyrrolidine Bisadducts with DNA Binding Activity." Organic Letters 14, no. 17 (August 24, 2012): 4450–53. http://dx.doi.org/10.1021/ol301946r.

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37

Nakamura, Yosuke, Masumi Taki, Seiji Tobita, Haruo Shizuka, Hajime Yokoi, Katsuya Ishiguro, Yasuhiko Sawaki, and Jun Nishimura. "ChemInform Abstract: Photophysical Properties of Various Regioisomers of [60]Fullerene-o-quinodimethane Bisadducts." ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918022.

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38

Lenes, Martijn, Gert-Jan A. H. Wetzelaer, Floris B. Kooistra, Sjoerd C. Veenstra, Jan C. Hummelen, and Paul W. M. Blom. "Fullerene Bisadducts for Enhanced Open-Circuit Voltages and Efficiencies in Polymer Solar Cells." Advanced Materials 20, no. 11 (June 4, 2008): 2116–19. http://dx.doi.org/10.1002/adma.200702438.

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39

Nakamura, Yosuke, Aya Asami, Toshio Ogawa, Seiichi Inokuma, and Jun Nishimura. "Regioselective Synthesis and Properties of Novel [60]Fullerene Bisadducts Containing a Dibenzocrown Ether Moiety." Journal of the American Chemical Society 124, no. 16 (April 2002): 4329–35. http://dx.doi.org/10.1021/ja0257063.

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40

Liu, Guangxin, Tiantian Cao, Yijun Xia, Bo Song, Yi Zhou, Ning Chen, and Yongfang Li. "Dihydrobenzofuran-C60 bisadducts as electron acceptors in polymer solar cells: Effect of alkyl substituents." Synthetic Metals 215 (May 2016): 176–83. http://dx.doi.org/10.1016/j.synthmet.2016.01.026.

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41

Zhang, Pu, Zhi Xin Guo, and Shuang Lv. "Synthesis and aggregation properties of amphiphilic mono and bisadducts of fullerene in aqueous solution." Chinese Chemical Letters 19, no. 9 (September 2008): 1039–42. http://dx.doi.org/10.1016/j.cclet.2008.06.017.

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42

Chen, Muqing, Yanyan Zeng, Gui Chen, and Yongfu Qiu. "Highly Regioselective Synthesis of Bisadduct[C70] Additive toward the Enhanced Performance of Perovskite Solar Cells." Nanomaterials 12, no. 14 (July 9, 2022): 2355. http://dx.doi.org/10.3390/nano12142355.

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Анотація:

The high-regioselective synthesis of bisadducts based on low-symmetry C70 has been a challenging work due to the large amount of formed regioisomers, which require tedious separation procedures for isomeric purity and block their application in different fields. Herein, we successfully obtained a novel 1, 2, 3, 4-bis(triazolino)fullerene[C70] 2 with high regioselectivity by the rigid tether-directed regioselective synthesis strategy and the corresponding molecular structure was unambiguously confirmed by single-crystal X-ray crystallography characterization. The crystal data clearly show that the addition occurs at the domain of corannulene moiety at the end of ellipse C70 as well as the 1, 2, 3, 4-addition sites located at one hexagonal ring with a [6,6]-closed addition pattern. Furthermore, 2 was applied as an additive of perovskite layer to construct MAPbI3-based regular (n-i-p) perovskite solar cells, affording the power conversion efficiency (PCE) of 18.59%, which is a 7% enhancement relative to that of control devices without additive.

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43

Kokubo, Ken, Riyah S. Arastoo, Takumi Oshima, Chun-Chih Wang, Yuan Gao, Hsing-Lin Wang, Hao Geng, and Long Y. Chiang. "Synthesis and Regiochemistry of [60]Fullerenyl 2-Methylmalonate Bisadducts and their Facile Electron-Accepting Properties." Journal of Organic Chemistry 75, no. 13 (July 2, 2010): 4574–83. http://dx.doi.org/10.1021/jo1007674.

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44

Qian, Ding-Quan, Henry J. Shine, Ilse Y. Guzman-Jimenez, John H. Thurston, and Kenton H. Whitmire. "Mono- and Bisadducts from the Addition of Thianthrene Cation Radical Salts to Cycloalkenes and Alkenes." Journal of Organic Chemistry 67, no. 12 (June 2002): 4030–39. http://dx.doi.org/10.1021/jo0104633.

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45

Pasimeni, L., U. Segre, M. Ruzzi, M. Maggini, M. Prato, and K. Kordatos. "Preferential Orientation of Fulleropyrrolidine Bisadducts in E7 Liquid Crystal: A Time-Resolved Electron Paramagnetic Resonance Study." Journal of Physical Chemistry B 103, no. 51 (December 1999): 11275–81. http://dx.doi.org/10.1021/jp9927000.

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46

Corvaja, C., L. Franco, and M. Mazzoni. "Chemically induced dynamic electron polarization of C60 nitroxide bisadducts and spin multiplicity of their excited states." Applied Magnetic Resonance 20, no. 1-2 (February 2001): 71–83. http://dx.doi.org/10.1007/bf03162311.

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47

Kim, Youngkwon, Chul-Hee Cho, Hyunbum Kang, Ki-Hyun Kim, Sunhee Park, Tae Eui Kang, Kwangyong Park, and Bumjoon J. Kim. "Benzocyclobutene-fullerene bisadducts as novel electron acceptors for enhancing open-circuit voltage in polymer solar cells." Solar Energy Materials and Solar Cells 141 (October 2015): 87–92. http://dx.doi.org/10.1016/j.solmat.2015.05.018.

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48

Nakamura, Yosuke, Aya Asami, Seiichi Inokuma, Toshio Ogawa, Munehiro Kikuyama, and Jun Nishimura. "Regioselective synthesis and complexation behavior of novel [60]fullerene bisadducts containing dibenzo-18-crown-6 moiety." Tetrahedron Letters 41, no. 13 (March 2000): 2193–97. http://dx.doi.org/10.1016/s0040-4039(00)00134-9.

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Lu, Qing, David I. Schuster, and Stephen R. Wilson. "Preparation and Characterization of Six Bis(N-methylpyrrolidine)−C60Isomers: Magnetic Deshielding in Isomeric Bisadducts of C60." Journal of Organic Chemistry 61, no. 14 (January 1996): 4764–68. http://dx.doi.org/10.1021/jo960466t.

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