Relevant bibliographies by topics / Dichloroanthracene

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Dichloroanthracene'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Dichloroanthracene"

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Lamm, Jan-Hendrik, Philipp Niermeier, Leif Körte, Beate Neumann, Hans-Georg Stammler, and Norbert Mitzel. "Improved Access to 1,8-Dichloro-10-(ethynyl)anthracene: A Useful Building Block for (Semi-)rigid Organic Frameworks." Synthesis 50, no. 10 (2018): 2009–18. http://dx.doi.org/10.1055/s-0036-1591925.

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An easy access to 1,8-dichloro-10-(ethynyl)anthracene is reported, which is widely applicable for building up rigid linkers between two 1,8-dichloroanthracene units. For this, 1,8-dichloroanthren-10(9H)-one was reacted with ethynylmagnesium bromide in the presence of CeCl3; the yield was 65%. This building block was used as a substrate in (cross-)coupling reactions and some examples of linked 1,8-dichloroanthracen-10-yls (e.g., 1,8-bis[(1,8-dichloroanthracen-10-yl)-ethynyl]naphthalene or 1,2-bis[(1,8-dichloroanthracen-10-yl)ethynyl]-benzene) were synthesized in good to moderate yields. Linked
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Benites, M. del R., A. W. Maverick, and F. R. Fronczek. "1,8-Dichloroanthracene." Acta Crystallographica Section C Crystal Structure Communications 52, no. 3 (1996): 647–48. http://dx.doi.org/10.1107/s0108270195014673.

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Mitzel, Norbert, Philipp Niermeier, Jan-Hendrik Lamm, Marvin Linnemannstöns, Beate Neumann та Hans-Georg Stammler. "Syntheses, Solid State Structures and Photochemistry of α,ω-Bis-[(1,8-dichloroanthracen-10-yl)dimethylsilyl]alkanes". Synthesis 50, № 15 (2018): 3041–47. http://dx.doi.org/10.1055/s-0037-1610128.

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Starting from 10-bromo-1,8-dichloroanthracene, a series of 1,8-dichlorinated anthracene derivatives, flexibly bridged in position 10 by –Me2Si– and –Me2Si–(CH2) n –SiMe2– linker units, were synthesised. The linked anthracenes were generated by converting (1,8-dichloroanthracen-10-yl)lithium with chlorosilanes in salt-elimination reactions. The bichromophors were tested in UV light induced photo reactions. None of the new compounds yielded any intra- or intermolecular photoproduct. All α,ω-(dimethylsilyl)alkane-linked bisanthracenes decomposed to give 1,8-dichloro-9-hydroxyanthracen-10(9H)-one
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Müller, Peter, Frank R. Fronczek, Stacey J. Smith, Teresa Mako, and Mindy Levine. "Two polymorphs of 1,8-dichloroanthracene." Acta Crystallographica Section C Crystal Structure Communications 69, no. 2 (2013): 199–203. http://dx.doi.org/10.1107/s0108270113001790.

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A second, monoclinic, polymorph of the title compound, C14H8Cl2, has been found. In addition to the structure of this monoclinic form, the structure of the previously described orthorhombic form [Desvergne, Chekpo & Bouas-Laurent (1978).J. Chem. Soc. Perkin Trans. 2, pp. 84–87; Benites, Maverick & Fronczek (1996).Acta Cryst.C52, 647–648] has been redetermined at low temperature and using modern methods. The low-temperature structure of the orthorhombic form is of significantly higher quality than the previously published structure and additional details can be derived. A comparison of
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5

Mizuno, Ken-ichi. "Exciton Dynamics in β-9,10-Dichloroanthracene". Journal of the Physical Society of Japan 59, № 4 (1990): 1458–73. http://dx.doi.org/10.1143/jpsj.59.1458.

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6

Beletskaya, Irina P., and A. D. Averin. "Palladium-catalyzed arylation of linear and cyclic polyamines." Pure and Applied Chemistry 76, no. 9 (2004): 1605–19. http://dx.doi.org/10.1351/pac200476091605.

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Synthetic protocols for the palladium-catalyzed arylation of various linear and cyclic polyamines and polyoxapolyamines has been worked out. Pd(0) and Pd(II)complexes with such phosphine ligands as dppf, BINAP, PPF-OMe, P(tBu)3,2-ditert-butylphosphino-1,1'-biphenyl have been explored in the catalytic amination reactions. Monoamination of chloro-, bromo-, and iodoarenes with di-, tri-, and tetraamines have been carried out, conditions for di- and polyarylation of linear polyamines have been elaborated. Successful arylation of 1,4,7,10-tetraazacyclododecane (cyclene) and 1,4,8,11-tetraazacyclote
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7

Pentlehner, D., and A. Slenczka. "Electronic spectroscopy of 9,10-dichloroanthracene inside helium droplets." Journal of Chemical Physics 138, no. 2 (2013): 024313. http://dx.doi.org/10.1063/1.4773894.

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8

Lederer, F. J., F. F. Graupner, B. Maerz, M. Braun, and W. Zinth. "Excimer formation in 9,10-dichloroanthracene – Solutions and crystals." Chemical Physics 428 (January 2014): 82–89. http://dx.doi.org/10.1016/j.chemphys.2013.11.005.

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9

del Rosario Benites, María, Frank R. Fronczek та Andrew W. Maverick. "Reduction during π-(cyclopentadienyliron) complexation of 1,8-dichloroanthracene". Journal of Organometallic Chemistry 516, № 1-2 (1996): 17–24. http://dx.doi.org/10.1016/0022-328x(95)06086-c.

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10

Saltiel, J., W. K. Smothers, K. S. Schanze, S. A. Charman, and R. Bonneau. "2,5-Dimethyl-2,4-hexadiene induced photodechlorination of 9,10-dichloroanthracene." Photochemical & Photobiological Sciences 8, no. 6 (2009): 856. http://dx.doi.org/10.1039/b821683e.

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Dissertations / Theses on the topic "Dichloroanthracene"

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賴昱亮. "Design, synthesis and antitumor activity of 9-alkoxy-1, 5-dichloroanthracene analogs." Thesis, 2001. http://ndltd.ncl.edu.tw/handle/23235237199950998104.

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Conference papers on the topic "Dichloroanthracene"

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Mahajan, Aman, Sukhwinder Singh Brar, R. K. Bedi, Dinesh K. Aswal, and Anil K. Debnath. "Characterization Of Hot Wall Grown 9, 10-Dichloroanthracene Films For Light Emitting Applications." In INTERNATIONAL CONFERENCE ON PHYSICS OF EMERGING FUNCTIONAL MATERIALS (PEFM-2010). AIP, 2010. http://dx.doi.org/10.1063/1.3530475.

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