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Journal articles on the topic 'Anthryl'

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Published: 4 June 2021

Last updated: 19 February 2022

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1

Aotake, Tatsuya, Mitsuharu Suzuki, Naoki Aratani, Junpei Yuasa, Daiki Kuzuhara, Hironobu Hayashi, Haruyuki Nakano, Tsuyoshi Kawai, Jishan Wu, and Hiroko Yamada. "Correction: 9,9′-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals." Chemical Communications 51, no. 24 (2015): 5124. http://dx.doi.org/10.1039/c5cc90112j.

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2

Li, Bao-Lin, Zhen-Guo Zhang, Wei Wang, Jin Li, and Chou-Wen Wang. "Solvent-free Friedel-Crafts Reaction for Regioselective Synthesis of Ethyl (9-Anthryl)glyoxylate and Chiral Resolution of (±)-(9-Anthryl)hydroxyacetic Acid." Zeitschrift für Naturforschung B 63, no. 1 (January 1, 2008): 77–82. http://dx.doi.org/10.1515/znb-2008-0111.

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A green chemistry-based highly regioselective synthesis of ethyl (9-anthryl)glyoxylate was achieved by solvent-free Friedel-Crafts reaction at r. t. Several derivatives of ethyl (9-anthryl)glyoxylate were also synthesized. Ethyl (9-anthryl)hydroxyacetate was obtained almost quantitatively by reduction of ethyl (9-anthryl)glyoxylate with NaBH4, and (9-anthryl)methoxyacetic acid was prepared by methylation of ethyl (9-anthryl)hydroxyacetate with CH3I in the presence of Ag2O and hydrolysis of ethyl (9-anthryl)methoxyacetate. The hydrolysis of ethyl (9-anthryl)hydroxyacetate gave racemic (9-anthryl)hydroxyacetic acid, and the racemate was successfully resolved by crystallization of the diastereomeric salts resulting from the reaction of (±)-(9-anthryl)hydroxyacetic acid with (-)-ephedrine. As a byproduct, crystals containing racemic (±)-(9-anthryl)hydroxyacetate and protonated (-)-ephedrine were isolated and their structures determined by X-ray diffraction.

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3

Becker, HD, BW Skelton, and AH White. "Molecular Topology of Di(9-Anthryl)Ethanedione (9,9'-Anthril) and Some Generically Related Cyclic 1,2-Diketones." Australian Journal of Chemistry 44, no. 2 (1991): 181. http://dx.doi.org/10.1071/ch9910181.

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The molecular structures of di (9-anthryl) ethanedione (9,9′-anthril) and those of four 1,2-diketones derived from 9,9′-anthril by way of intramolecular cycloadditions were investigated by single-crystal X-ray diffraction studies. Two crystal modifications of 9,9′-anthril were available and found to differ in the dihedral angles (43.9 and 178.3°) about the 1,2-dicarbonyl moiety. The 1,2-dicarbonyl group of the cyclobutanedione moiety in the anthril 4π+4π cyclomer is associated with a dihedral angle of 2.6°. In the anthril isomer derived by 4π+2π cycloaddition, an exceptionally long single bond is indicative of molecular strain. The molecular structures of a keto enol and of a novel 1,2-diketo substituted triptycene, both obtained from the 4π+2π cyclomer by acid-catalysed rearrangement and dehydrogenation, respectively, were established. The topological and spectroscopic differences between the keto en01 and its 1,2-diketo precursor are discussed.

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4

Becker, HD, V. Langer, BW Skelton, and AH White. "Molecular Structures of Di(9-anthryl)Methanol and Di(9-anthryl) Ketone." Australian Journal of Chemistry 42, no. 4 (1989): 603. http://dx.doi.org/10.1071/ch9890603.

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The molecular structures of di(9-anthryl)methanol (1) and di(9-anthryl) ketone (2) have been established by X-ray diffraction. The asymmetric unit of di(anthryl)methanol consists of two molecules in which the dihedral angle between the anthracene moieties is 81.4 and 86.3 respectively; steric interaction between the anthracene moieties results in them subtending angles of 115.0(7) and 115.8(8)� at the central carbon atom, and with unsymmetrical exocyclic angles at their point of attachment. In di(9-anthryl) ketone the planes of the anthracene systems are twisted out of the plane of the carbonyl group by 48.8 and 52.2� respectively, so that the dihedral angle between the two aromatic ring systems is 87.3�. The structures of di(anthryl)methanol and di(anthryl) ketone are discussed with respect to their different modes of photochemical isomerization by intramolecular cycloaddition.

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5

Takahashi, Koji, Yoshinobu Nishimura, Tatsuo Arai, Shiki Yagai, Akihide Kitamura, and Takashi Karatsu. "Photophysics and photochemistry of positionally isomeric 1,2-dianthryltetramethyldisilanes: Investigation of anthryl–anthryl and anthryl–SiSi interactions." Journal of Photochemistry and Photobiology A: Chemistry 218, no. 2-3 (February 2011): 204–12. http://dx.doi.org/10.1016/j.jphotochem.2010.12.021.

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6

Becker, HD, L. Hansen, BW Skelton, and AH White. "Molecular Topology of 1,2-Substituted (E) and (Z)-1,2-Di(9-anthryl)ethenes." Australian Journal of Chemistry 41, no. 10 (1988): 1557. http://dx.doi.org/10.1071/ch9881557.

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Single-crystal X-ray structure determinations have been carried out on six derivatives of (E)- and (Z)-1,2-di(9-anthryl) ethenes in which the central carbon-carbon double bond is additionally substituted, establishing the molecular topology in terms of the angles between the planes of the anthryl moieties and the plane of the central ethene bond. In general terms, substitution increases the torsion angle about the anthryl-ethene single bond by up to approximately 30°, so that the anthryl and ethene planes lie virtually orthogonal.

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7

Polo-Cerón, Dorian, Santiago Gómez-Ruiz, Sanjiv Prashar, Mariano Fajardo, Antonio Antiñolo, and Antonio Otero. "Synthesis of Bulky Zirconocene Dichloride Compounds and Their Applications in Olefin Polymerization." Collection of Czechoslovak Chemical Communications 72, no. 5-6 (2007): 747–63. http://dx.doi.org/10.1135/cccc20070747.

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The bulky substituted cyclopentadienyllithium derivatives, LiC5H4(CHMeR) (R = C6H5 (1), 1-naphthyl (2), 9-anthryl (3)), were synthesized from the reaction of 6-phenylfulvene, 6-(1-naphthyl)fulvene or 6-(9-anthryl)fulvene with LiMe. The ansa-bis(cyclopentadiene) ligands Me2Si(C5HMe4){C5H4(CHMeR)} (R = C6H5 (4), 1-naphthyl (5), 9-anthryl (6)), and their lithium derivatives Li2(Me2Si(C5Me4){C5H3(CHMeR)}) (R = C6H5 (7), 1-naphthyl (8), 9-anthryl (9)) have been prepared. The zirconocene complexes, [Zr(η5-C5H5){η5-C5H4- (CHMeR)}Cl2] (R = C6H5 (10), 1-naphthyl (11), 9-anthryl (12)) and [Zr{η5-C5H4(CHMeR)}2Cl2] (R = C6H5 (13), 1-naphthyl (14), 9-anthryl (15)), were synthesized by the reaction of lithium derivatives 1-3 and [Zr(η5-C5H5)Cl3] or ZrCl4, respectively. The reaction of the lithium ansa-derivatives 7-9 and zirconium tetrachloride yielded the ansa-zirconocene complexes, [Zr(Me2Si(η5-C5Me4){η5-C5H3(CHMeR)})Cl2] (R = C6H5 (16), 1-naphthyl (17), 9-anthryl (18)). The zirconocene complexes have been tested in the polymerization of ethene and propene. The polymerization of propene with the ansa-zirconocene catalysts 16-18 gave polypropylene with 70% mmmm pentads and the symmetric zirconocene catalysts 13-15 30-60% mmmm pentads.

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8

Agrahari, Aditya, Patrick O. Wagers, Steven M. Schildcrout, John Masnovi, and Wiley J. Youngs. "Crystal structure of 9-methacryloylanthracene." Acta Crystallographica Section E Crystallographic Communications 71, no. 4 (March 11, 2015): 357–59. http://dx.doi.org/10.1107/s2056989015004090.

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In the title compound, C18H14O, with systematic name 1-(anthracen-9-yl)-2-methylprop-2-en-1-one, the ketonic C atom lies 0.2030 (16) Å out of the anthryl-ring-system plane. The dihedral angle between the planes of the anthryl and methacryloyl moieties is 88.30 (3)° and the stereochemistry about the Csp2—Csp2bond in the side chain istransoid. In the crystal, the end rings of the anthryl units in adjacent molecules associate in parallel–planar orientations [shortest centroid–centroid distance = 3.6320 (7) Å]. A weak hydrogen bond is observed between an aromatic H atom and the O atom of a molecule displaced by translation in thea-axis direction, forming sheets of parallel-planar anthryl groups packing in this direction.

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9

Zhang, Lei, Yilong He, Na Zhang, Daosheng Liu, Jiao Han, and Weitao Gong. "Construction of a novel INHIBIT logic gate through a fine-tuned assembly of anthryl fluorophores via selective anion recognition and host–guest interactions." RSC Advances 6, no. 1 (2016): 805–9. http://dx.doi.org/10.1039/c5ra20120a.

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A novel ligand containing of anthryl fluorophore was achieved. The assembly and disassembly of anthryl fluorophore by Pi and β-CD as chemical inputs and emission around 500 nm as output resulted in the construction of novel INHIBIT gate.

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10

Aotake, Tatsuya, Mitsuharu Suzuki, Naoki Aratani, Junpei Yuasa, Daiki Kuzuhara, Hironobu Hayashi, Haruyuki Nakano, Tsuyoshi Kawai, Jishan Wu, and Hiroko Yamada. "9,9′-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals." Chemical Communications 51, no. 31 (2015): 6734–37. http://dx.doi.org/10.1039/c4cc10104a.

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11

Hirsch, T., H. Port, and H. C. Wolf. "Time Resolved Photoinduced Charge Separation in Pyridinium Substituted Anthryl-Methylenes and Anthryl-Polyenes." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 283, no. 1 (June 1996): 203–8. http://dx.doi.org/10.1080/10587259608037887.

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12

Singh, Anil K., and Mita Roy. "Bacteriorhodopsin analogue from anthryl chromophores." Canadian Journal of Chemistry 68, no. 3 (March 1, 1990): 383–89. http://dx.doi.org/10.1139/v90-058.

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Preparation and properties of the bacteriorhodopsin (bR) analogue having the 3,7-dimethyl-9-(9-anthryl)-2E,4E,6E,8E-nonatetraenal (12) chromophore is described. Synthesis of the chromophore has been achieved by successive introduction of C5 units to 9-anthraldehyde (3) via the Horner reaction. The all-trans chromophore has been characterized by its ultraviolet–visible and 1H nuclear magnetic resonance spectra. Incubation of 12 with bacterioopsin suspension (prepared by photobleaching of bR isolated from Halobacteriumhalobium) at ambient temperature in the dark gave the new bR analogue 15, which showed an absorption band at 545 nm, and an opsin shift of 5575 cm−1. The new pigment is stable to hydroxylamine in the dark. It showed light–dark adaptation with the light-adapted form absorbing at a slightly red-shifted value of 550 nm. All-trans-retinal did not replace the anthryl chromophore in competitive bindings. Photolysis of the bR analogue 15, followed by difference spectrophotometric analysis, indicated formation of a photoproduct with an absorption band near 400 nm. The results are discussed in terms of the stereoelectronic requirements of the bR reaction centre. Keywords: bacteriorhodopsin (bR), retinal analogue, reconstitution, opsin shift (OS), external point charge model (EPC).

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13

Singh, Anil K., and Mita Roy. "Fluorescence studies on anthryl bacteriorhodopsins." Journal of Photochemistry and Photobiology B: Biology 8, no. 3 (February 1991): 325–35. http://dx.doi.org/10.1016/1011-1344(91)80089-z.

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14

Arslan, Mustafa, Erol Asker, John Masnovi, and Ronald J. Baker. "10,10′-Dinitro-10,10′-(butane-1,4-diyl)dianthracen-9(10H)-one." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (June 14, 2006): o2819—o2821. http://dx.doi.org/10.1107/s160053680602157x.

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The title compound, C32H24N2O6, was obtained as the decomposition product of (E,E)-1,4-bis[9,10-dihydro-9-nitro-10-(trinitromethyl)-9-anthryl]butane, which was synthesized via a photochemical reaction of 1,4-bis(9-anthryl)butane with tetranitromethane. The asymmetric unit contains one half-molecule; the complete molecule is generated by a center of inversion. The crystal packing is determined mainly by intermolecular C—H...O interactions.

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15

Mrozek, Justyna, Katarzyna Guzow, Emilia Sikorska, and Wiesław Wiczk. "Influence of amino acid sequence on the interaction of short peptides containing 3-[2-(9-anthryl)benzoxazol-5-yl]-alanine with β-cyclodextrin." Open Chemistry 9, no. 6 (December 1, 2011): 1046–55. http://dx.doi.org/10.2478/s11532-011-0103-x.

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AbstractThe influence of peptide sequence and Leu chirality in linear and cyclic peptides containing 3-[2-(9-anthryl)benzoxazol-5-yl]alanine on interaction with β-cyclodextrin were studied using fluorescence and NMR spectroscopy. The analysis of enthalpy-entropy compensation effect (α=1.05±0.02 and TΔS00=15.1±0.5 kJ mol−1) indicates that the entropic contribution connected with the solvent reorganization is the major factor governing the peptides-β-cyclodextrin complexation. Moreover, spatial orientation of guest-host molecule depends more than association constant on Leu residue configuration. However, the cyclization of the peptide chain substantially decrease the association constant with β-CD. An analysis of 2D NMR spectra reveals that inclusion complex is formed by penetration of cyclodextrin cavity from wider and narrow rims by anthryl group in the case of Box(Ant)-SPKL or anthryl and Leu residues for Box(Ant)-SPK(D)L analogue.

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16

Toyota, Shinji, Mai Nishiuchi, Taisei Iwata, Tomokazu Yamauchi, Tetsuo Iwanaga, and Masashi Hasegawa. "Synthesis, structures, and properties of 2,5-dianthrylthiophene derivatives." Canadian Journal of Chemistry 95, no. 3 (March 2017): 286–91. http://dx.doi.org/10.1139/cjc-2016-0391.

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The title thiophene derivatives bearing two 9-, 1-, or 2-anthryl groups were synthesized by cyclization of the corresponding 1,3-diynes with sodium sulfide or by Suzuki–Miyaura coupling. X-ray analysis and DFT calculations revealed that the molecules adopt nonplanar conformations depending on the steric demand of the anthryl groups. The dihedral angles between the arene units are an important contributor to the photophysical properties in the electronic spectra as well as the electrochemical data.

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17

Lin, Chih-Hsiu, and Krishnan Radhakrishnan. "Synthesis of Anthryl Sulfides from Anthryl Methyl Ethers via Acid-Catalyzed Ether-Sulfide Exchange Reaction." Synlett, no. 14 (2005): 2179–82. http://dx.doi.org/10.1055/s-2005-872268.

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18

Becker, H., L. Hansen, BW Skelton, and AH White. "(E)-1-(9-Anthryl)-2-(10-methyl-9-anthryl)ethene: Molecular Structure and Spectroscopic Properties." Australian Journal of Chemistry 38, no. 5 (1985): 809. http://dx.doi.org/10.1071/ch9850809.

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(E)-1-(9-Anthryl)-2-(10-methyl-9-anthryl) ethelle has been synthesized from 10-methyl-9-anthraldehyde and (9-anthrylmethyl) triphenylphosphonium bromide, and its crystal structure has been determined by X-ray diffraction. Its molecular geometry was found to be such as to have the planes of the two anthracene moieties form an angle of 70.8°, the plane of the ethene bond bring twisted out of the planes of the anthracenes by an angle of about 55°. The intermolecular arrangement of parallel adjacent molecules in the crystal lattice is characterized by shifts about the short and long axes of the anthracenes. The excimer-like crystal fluorescence is attributed to the interplanar distance of 3.5 Ǻ between anthracene π- systems in parallel adjacent molecules. Crystals are triclinic, Pī , a 12.95(1), b 9.316(6), c 9.098(9) Ǻ, α 86.17(7), β 72.26(7), γ 74.61(6)°,Z 2; R was 0.054 for 1059 independent 'observed' reflections.

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19

Li, Bao-Lin, Zhen-Guo Zhang, Li-Li Du, and Wei Wang. "Chiral resolutions of (9-anthryl)methoxyacetic acid and (9-anthryl)hydroxyacetic acid by capillary electrophoresis." Chirality 20, no. 1 (January 2008): 35–39. http://dx.doi.org/10.1002/chir.20485.

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20

Becker, HD, L. Hansen, BW Skelton, H. Sorensen, and AH White. "Formation and Molecular-Structures of meso-1,2-Bis(9-anthryl)-1,2-diacetoxyethanes." Australian Journal of Chemistry 42, no. 7 (1989): 1177. http://dx.doi.org/10.1071/ch9891177.

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The molecular structures of meso-1,2-diacetoxy-1,2-di(9-anthryl)ethane (1) and meso-1,2-diacetoxy-1,2-di(10-acetoxy-9-anthryl)ethane (2) have been established by X-ray diffraction. Their molecular conformations are characterized by a staggered arrangement of substituents about the central ethane linkage, and anti-orientation of the anthracene moieties. The dianthrylethane derivative (1) was isolated in two crystalline modifications, (1a) and (1b), whose different crystal luminescence properties are correlated with the differences in packing pattern.

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21

dos Santos, M. C., and D. A. Silva-Filho. "Electronic structure of 9-anthryl-oligothiophenes." Synthetic Metals 121, no. 1-3 (March 2001): 1493–94. http://dx.doi.org/10.1016/s0379-6779(00)01062-6.

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22

Stoeckli-Evans, H., and R. A. Hann. "(−)-2-Bornyl 3-(9-anthryl)propionate." Acta Crystallographica Section C Crystal Structure Communications 43, no. 7 (July 15, 1987): 1350–53. http://dx.doi.org/10.1107/s0108270187091911.

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23

Singh, Anil K., and Mita Roy. "Fluorescence studies on some anthryl compounds." Journal of Photochemistry and Photobiology A: Chemistry 51, no. 3 (April 1990): 327–39. http://dx.doi.org/10.1016/1010-6030(90)87067-l.

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24

Becker, H., BW Skelton, and AH White. "Photochemical Isomerization of (E,Z)-1,5-Bis(9-anthryl)penta-1,4-dien-3-one and its Intramolecular Diels-Alder Adduct." Australian Journal of Chemistry 38, no. 10 (1985): 1471. http://dx.doi.org/10.1071/ch9851471.

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Photoexcitation of (E,Z)-1,5-bis(9-anthryl)penta-1,4-dien-3-one (2) leads to 4-(9-anthryl)-4,5-dihydro-5,9b[1′,2′]-benzeno-9bH- benz [e]indene-3(3aH)-one (3) which is formed by an intramolecular Diels -Alder addition. Upon irradiation, (3) undergoes a skeletal rearrangement to give a product (4), rationalized in terms of a stepwise reaction involving diradical intermediates. The molecular structure of (4) has been established by X-ray diffraction, and the stereochemistry of (3) deduced from the results of X-ray diffraction studies of its reduction products (5) and (6).

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25

Katla, Jagadish, Akshay J. M. Nair, Abhijeet Ojha, and Sriram Kanvah. "Organogels composed of trifluoromethyl anthryl cyanostyrenes: enhanced emission and self-assembly." Photochemical & Photobiological Sciences 17, no. 4 (2018): 395–403. http://dx.doi.org/10.1039/c7pp00362e.

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26

Han, Dongdong, Hang Lu, Wensi Li, Yonghao Li, and Shengyu Feng. "Light- and heat-triggered reversible luminescent materials based on polysiloxanes with anthracene groups." RSC Advances 7, no. 89 (2017): 56489–95. http://dx.doi.org/10.1039/c7ra12201b.

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27

Sontakke, Vyankat A., Anup N. Kate, Sougata Ghosh, Piyush More, Rajesh Gonnade, Navanath M. Kumbhar, Anupa A. Kumbhar, Balu A. Chopade, and Vaishali S. Shinde. "Synthesis, DNA interaction and anticancer activity of 2-anthryl substituted benzimidazole derivatives." New Journal of Chemistry 39, no. 6 (2015): 4882–90. http://dx.doi.org/10.1039/c4nj02415j.

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28

Wang, Chin-Li, Min Zhang, Yu-Hsin Hsiao, Chuan-Kai Tseng, Chia-Lin Liu, Mingfei Xu, Peng Wang, and Ching-Yao Lin. "Porphyrins bearing a consolidated anthryl donor with dual functions for efficient dye-sensitized solar cells." Energy & Environmental Science 9, no. 1 (2016): 200–206. http://dx.doi.org/10.1039/c5ee02505b.

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29

Yang, Mingdi, Yan Zhang, Weiju Zhu, Huizhen Wang, Jing Huang, Longhuai Cheng, Hongping Zhou, Jieying Wu, and Yupeng Tian. "Difunctional chemosensor for Cu(ii) and Zn(ii) based on Schiff base modified anthryl derivative with aggregation-induced emission enhancement and piezochromic characteristics." Journal of Materials Chemistry C 3, no. 9 (2015): 1994–2002. http://dx.doi.org/10.1039/c4tc02616k.

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30

Li, Ye-Xin, Zhen-Feng Yu, Cun-Zhao Zhu, Xiao-Feng Yang, Yong Nie, Yu Cui, and Guo-Xin Sun. "Three new metastable polymorphs of 1-(9-anthryl)-2-(1-naphthyl)ethylene and the polymorph-dependent phase transition and fluorescence change properties." CrystEngComm 21, no. 9 (2019): 1512–18. http://dx.doi.org/10.1039/c8ce01935e.

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31

Tomioka, Hideo, Junichi Nakajima, Hidehiko Mizuno, Eiji Iiba, and Katsuyuki Hirai. "Article." Canadian Journal of Chemistry 77, no. 5-6 (June 1, 1999): 1066–76. http://dx.doi.org/10.1139/v99-092.

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A series of triplet 9-triptycyl(aryl)carbenes, where aryl groups are phenyl, 1- and 2-naphthyl, and 9-anthryl, is generated by photolysis of the corresponding diazomethanes and observed directly by spectroscopic means. Their structures are characterized by electron spin resonance (ESR) spectroscopy in a 2-methyltetrahydrofuran matrix at 77 K, and the reactivities are investigated by laser flash photolysis in degassed benzene solution at room temperature. Comparison of the data with other arylcarbenes bearing a series of substituents, i.e., hydrogen, phenyl, naphthyl, and anthryl groups, revealed an interesting relationship between structures and reactivities of triplet arylcarbenes.Key words: steric protection, stability of triplet carbenes, electron spin resonance, laser flash photolysis, structure-reactivity relationship.

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32

UCHIUMI, Akira, Akiko TAKATSU, and Hisashi TANAKA. "Metal Complex Formation of Some Anthryl Formazans." Analytical Sciences 7, no. 3 (1991): 459–62. http://dx.doi.org/10.2116/analsci.7.459.

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33

Kharlanov, Vladimir A., Wolfgang Rettig, Michael I. Knyazhansky, and Nadezhda Makarova. "Multiple emission of N-(1-anthryl)-pyridinium." Journal of Photochemistry and Photobiology A: Chemistry 103, no. 1-2 (February 1997): 45–50. http://dx.doi.org/10.1016/s1010-6030(96)04486-3.

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34

Kraicheva, Ivanka, Ivelina Tsacheva, Elitsa Vodenicharova, Emil Tashev, and Kolio Troev. "Diethyl [(9-anthryl)(4-methylanilino)methyl]phosphonate." Acta Crystallographica Section E Structure Reports Online 67, no. 8 (July 9, 2011): o1980. http://dx.doi.org/10.1107/s1600536811025943.

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35

Buruiana, Tinca, A. Airinei, E. C. Buruiana, and Gabriela Robila. "Polyurethane cationomers containing anthryl and nitroaromatic chromophores." European Polymer Journal 33, no. 6 (June 1997): 877–80. http://dx.doi.org/10.1016/s0014-3057(96)00284-4.

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36

Kansikas, Jarno, and Kaija Sipilä. "Di-9-anthryl disulfide at 193 K." Acta Crystallographica Section C Crystal Structure Communications 56, no. 1 (January 15, 2000): 72–73. http://dx.doi.org/10.1107/s0108270199012846.

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37

Takahashi, Yasutake, Masaaki Tomura, Ken-ichi Yoshida, Shigeru Murata, and Hideo Tomioka. "Triplet Di(9-anthryl)carbene Undergoes Trimerization." Angewandte Chemie 39, no. 19 (October 2, 2000): 3478–80. http://dx.doi.org/10.1002/1521-3773(20001002)39:19<3478::aid-anie3478>3.0.co;2-l.

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38

Takahashi, Yasutake, Masaaki Tomura, Ken-ichi Yoshida, Shigeru Murata, and Hideo Tomioka. "Triplet Di(9-anthryl)carbene Undergoes Trimerization." Angewandte Chemie 112, no. 19 (October 2, 2000): 3620–22. http://dx.doi.org/10.1002/1521-3757(20001002)112:19<3620::aid-ange3620>3.0.co;2-b.

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39

Bylińska, Irena, Artur Sikorski, and Wiesław Wiczk. "4-(9-Anthryl)-2-methylbutyn-2-ol." Acta Crystallographica Section E Structure Reports Online 64, no. 2 (January 23, 2008): o484—o485. http://dx.doi.org/10.1107/s1600536808001542.

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40

Roje, Marin, Zdenko Hameršak, and Vitomir Šunjić. "EFFICIENT RESOLUTION OF (±)-1-(9-ANTHRYL)ETHYLAMINE." Synthetic Communications 32, no. 22 (January 2002): 3413–17. http://dx.doi.org/10.1081/scc-120014769.

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41

Reiners, I., and J. Martens. "Preparation of 1-(9-anthryl)-ethanol and 9-anthryloxirane via catalytic enantioselective reduction of prochiral 9-anthryl ketones." Tetrahedron: Asymmetry 8, no. 1 (January 1997): 27–28. http://dx.doi.org/10.1016/s0957-4166(96)00476-4.

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42

Cotrait, M., H. Allouchi, P. Marsau, A. Nourmamode, S. Grelier, and A. Castellan. "Studies on Aromatic Trichromophore Systems Incorporating Anthracene Moieties. III. Crystal Structures of 2-(9-Anthryl)-1-(9-anthrylmethyl)ethyl 2-(9-Anthryl)ethyl Succinate (A2A) and 2-(9-Anthryl)ethyl Acetate (AM) and Their Fluorescence in the Solid State." Australian Journal of Chemistry 49, no. 1 (1996): 13. http://dx.doi.org/10.1071/ch9960013.

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The structures of 2-(9-anthryl)-1-(9-anthrylmethyl)ethyl 2-(9 anthryl )ethyl succinate (A2A) and 2-(9-anthryl)ethyl acetate (AM) have been determined by X-ray diffraction, and the molecular fluorescence of the crystals has been established. The A2A crystal is triclinic while the AM crystal is monoclinic. A2A: Pī , a 18.514(5), b 11.802(3), c 10.836(3) Ǻ; α 99.63(2), β 85.75(2), γ 79.67(2)°, R 0.053 for 3547 observed reflections. AM: P21/c, a 12.566(2), b 12.991(2), c 8.805(2) Ǻ, β 97.84(1)°, R 0.040 for 1519 observed reflections. For the A2A molecule as for the previously studied A2PHEN and A2SC (see Part II), the bisanthracene moiety and a large part of the ester chain show similar conformations. The crystal cohesion is due to numerous van der Waals interactions in both compounds and to π intermolecular overlap between the anthracene moieties of neighbouring molecules of AM. The fluorescence emission of the AM crystal is of excimer type and correlates with the intermolecular stacking of the anthracene rings. In contrast, the emission from the A2A crystal was found to be very weak and with some similarity with the emission of the dilute solution. This is probably due to defects, not accounted for by the X-ray determination, permitting intramolecular interactions in the solid.

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43

Maria Maroń, Anna, Katarzyna Choroba, Tomasz Pedzinski, and Barbara Machura. "Towards better understanding of the photophysics of platinum(ii) coordination compounds with anthracene- and pyrene-substituted 2,6-bis(thiazol-2-yl)pyridines." Dalton Transactions 49, no. 38 (2020): 13440–48. http://dx.doi.org/10.1039/d0dt02650f.

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44

Shin, Eun Ju, and Seung Won Choi. "Photoisomerization behavior of 1-(9-anthryl)-2-(2-pyrazinyl)ethene, a diaza analogue of 1-(9-anthryl)-2-phenylethene." Journal of Photochemistry and Photobiology A: Chemistry 114, no. 1 (March 1998): 23–30. http://dx.doi.org/10.1016/s1010-6030(98)00197-x.

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45

Xu, Li, Peng-Fei Wang, Juan-Juan Zhang, Wei Wu, Jian-Wu Shi, Jing-Fang Yuan, Hui Han, and Hua Wang. "Synthesis and spectroscopic properties of propeller type 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine." RSC Advances 5, no. 64 (2015): 51745–49. http://dx.doi.org/10.1039/c5ra08833j.

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The novel propeller typed compound, 2,4,6-tri(anthracen-9-yl)-1,3,5-triazine was synthesized by using 9-anthryl lithium with 1,3,5-trichlorotriazine or 2-chloro-4,6-dimethoxy-1,3,5-triazine. It's interesting spectroscopic behaviors were also studied.

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46

Wang, Hui-Juan, Hao-Yang Zhang, Heng-Yi Zhang, Guoxing Liu, Xianyin Dai, Huang Wu, and Yu Liu. "Guest-induced supramolecular chirality transfer in [2]pseudorotaxanes: experimental and computational study." Organic & Biomolecular Chemistry 18, no. 38 (2020): 7649–55. http://dx.doi.org/10.1039/d0ob01347a.

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We constructed several [2]pseudorotaxanes via chiral binaphthalene crown ethers and achiral ammonium salts, and found that the binaphthalene groups can induce new CD signals only in the [2]pseudorotaxane between the hosts and the guest with anthryl.

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47

Sakurai, Hideki, Kenkichi Sakamoto, Akihiro Nakamura, and Mitsuo Kira. "PHOTOCHEMISTRY OF DI(9-ANTHRYL)DIMETHYLSILANE AND -GERMANE." Chemistry Letters 14, no. 4 (April 5, 1985): 497–98. http://dx.doi.org/10.1246/cl.1985.497.

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48

Kraicheva, Ivanka, Ivelina Tsacheva, Elitsa Vodenicharova, Emil Tashev, and Kolio Troev. "rac-Dimethyl [(9-anthryl)(4-methylanilino)methyl]phosphonate." Acta Crystallographica Section E Structure Reports Online 67, no. 8 (July 16, 2011): o2045. http://dx.doi.org/10.1107/s1600536811027711.

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49

Sweeting, Linda M., and Arnold L. Rheingold. "Crystal structure and triboluminescence. 1. 9-Anthryl carbinols." Journal of Physical Chemistry 92, no. 20 (October 1988): 5648–55. http://dx.doi.org/10.1021/j100331a022.

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50

Becker, H., BW Skelton, and AH White. "Molecular Geometry of 1,2-Bis(9-anthryl)acetylene." Australian Journal of Chemistry 38, no. 10 (1985): 1567. http://dx.doi.org/10.1071/ch9851567.

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The structure of 1,2-bis(9-anthryl)acetylene has been determined by single-crystal X-ray diffraction, being refined by least squares to a residual of 0.050 for 566 independent 'observed' reflections. Crystals are monoclinic, P21/c, a 12.432(5), b 5.112(1), c 18.758(8) Ǻ, β 126.58(2)°, Z 2. The molecule is centrosymmetric , with the two anthracene moieties coplanar. The spatial separation between H1/H8 and their centrosymmetric equivalents is 2.1 Ǻ. The length of the acetylenic bond is 1.193(10) Ǻ.

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