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Journal articles on the topic 'Anthracen'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Berg, David J., and Brendan Twamley. "Crystal structure of a binuclear mixed-valence ytterbium complex containing a 2-anthracene-substituted phenoxide ligand." Acta Crystallographica Section E Crystallographic Communications 75, no. 9 (2019): 1367–71. http://dx.doi.org/10.1107/s205698901901154x.

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Reaction of 2-(anthracen-9-yl)phenol (HOPhAn, 1) with divalent Yb[N(SiMe3)2]2·2THF in THF–toluene mixtures affords the mixed-valence YbII–YbIII dimer {[2-(anthracen-9-yl)phenolato-κO]bis(tetrahydrofuran)ytterbium(III)}-tris[μ-2-(anthracen-9-yl)phenolato]-κ4 O:O;κO:1,2-η,κO-{[2-(anthracen-9-yl)phenolato-κO]ytterbium(II)} toluene trisolvate, [Yb2(C20H13O)5(C4H8O)2]·3C7H7 or [YbIII(THF)2(OPhAn)](μ-OPhAn)3[YbII(OPhAn)]·3C7H7 (2), as the major product. It crystallized as a toluene trisolvate. The Yb—O bond lengths in the crystal structure of this dimer clearly identify the YbII and YbIII centres. I

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2

Boyd, Simon, Nuno M. Cabral, Kenneth P. Ghiggino, Martin J. Grannas, W. David McFadyen, and Peter A. Tregloan. "Nickel complexation and photophysics of alkylanthracenyl dioxocyclam macrocycle derivatives." Australian Journal of Chemistry 53, no. 8 (2000): 651. http://dx.doi.org/10.1071/ch00106.

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Ligands H2L in which (10-R-anthracen-9-yl)methyl moieties (R = H, Me, Et) are covalently joined (6-position) to the 5,7-dioxocyclam macrocycle framework have been prepared and their nickel(II) complexes isolated and characterized. X-Ray crystal structures of NiIIL (R = H, Me) complexes show that in both structures the anthracene moieties are folded around towards the mean plane of the macrocycles; dihedral angles between the mean anthracene and macrocyclic planes of c. 22˚ are subtended. 1H n.m.r. spectrometry indicates that the folded conformations are retained in solution. Absorption and flu

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3

Khanra, Somnath, Sabyasachi Ta, Milan Ghosh, Sudeshna Chatterjee, Pallabi Mukherjee, and Debasis Das. "Al3+ triggered aggregation induced emission of an anthracence based azine derivative in SDS medium." New Journal of Chemistry 44, no. 20 (2020): 8477–85. http://dx.doi.org/10.1039/d0nj00968g.

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Single crystal X-ray structurally characterized anthracene appended unsymmetrical azine derivative, viz. 4-(anthracen-9-ylmethylene-hydrazonomethyl)-2-methoxy-phenol (L5) shows Al<sup>3+</sup> assisted aggregation induced emission in SDS medium.

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4

Liu, Dan, Chenguang Li, Shujie Niu, et al. "A case study of tuning the crystal polymorphs of organic semiconductors towards simultaneously improved light emission and field-effect properties." Journal of Materials Chemistry C 7, no. 20 (2019): 5925–30. http://dx.doi.org/10.1039/c9tc01321k.

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Simultaneously improved light emission and field-effect performance were achieved for an anthracene derivative, 1,4-di(anthracen-9-yl)buta-1,3-diyne (DABD) in its β-phase crystals, suggesting their potential applications in integrated optoelectronic devices.

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5

Boyd, Simon, Kenneth P. Ghiggino, and W. David McFadyen. "Photochemistry of Anthracene-Appended Cobalt(III) Cyclam Complexes." Australian Journal of Chemistry 61, no. 8 (2008): 585. http://dx.doi.org/10.1071/ch08189.

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The photochemistry of two anthracene-appended cobalt(iii) cyclam complexes is explored with a view to demonstrate a photoactivated ligand release process. The ligand exchange processes that occur in the complexes cis-[CoL(NO2)(ONO)]+ and trans-[CoL(NO2)(ONO)]+ in which L = 6-(anthracen-9-ylmethyl)-1,4,8,11-tetraazacyclotetradecane were monitored upon illumination of the anthracenyl chromophore at 360 nm in the presence of a large excess of thiocyanate. The trans-[CoL(NO2)(ONO)]+ complex underwent a ligand exchange reaction in the absence of light and displayed an enhancement of the reaction up

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6

Kabay, Nilgün, Burak Doğan Bozer, Aslı Öztürk Kiraz, Yasemin Baygu, İzzet Kara, and Yaşar Gök. "Synthesis, characterization and structural computational investigation of novel Zn(II) phthalocyanines containing peripheral anthracene moieties." Journal of Porphyrins and Phthalocyanines 23, no. 07n08 (2019): 943–59. http://dx.doi.org/10.1142/s1088424619500913.

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New zinc(II) phthalocyanines (ZnPc-I and ZnPc-II) containing four peripheral anthracene pendant groups were synthesized by cyclotetramerization of (E)-4-(3-(4-((anthracen-9-yl-methylene)amino)phenoxy)propoxy)phthalonitrile and 4-(3-(4-((anthracen-9-ylmethyl)amino)phenoxy)propoxy)phthalonitrile. All compounds were characterized using a combination of analytical and spectroscopic techniques such 1H, [Formula: see text]C NMR, FT-IR, UV-vis and MS spectral data. The molecular geometry and gauge including atomic orbital (GIAO) 1H and [Formula: see text]C chemical shift values of the compounds in th

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7

Dong, Zhenming, Bo Liu, Xinxin Cui, and Yufang Liu. "2-(Anthracen-9-yl)-10-methoxybenzo[h]quinoline acetone hemisolvate." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2535. http://dx.doi.org/10.1107/s1600536812031807.

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The asymmetric unit of the title structure, C28H19NO·0.5C3H6O, comprises one 2-(anthracen-9-yl)-10-methoxybenzo[h]quinoline molecule and an acteone molecule with an occupany of 0.5. The solvent molecule is disordered around a centre of symmetry. Its occupancy was determined from NMR data and kept fixed during the refinement. The two conjugated ring systems of the molecule are almost perpendicular to each other; the interplanar angle between the anthracene and quinoline ring systems is 84.9 (2)°.

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8

Zainuri, Dian Alwani, Ibrahim Abdul Razak, and Suhana Arshad. "Crystal structures, DFT studies and UV–visible absorption spectra of two anthracenyl chalcone derivatives." Acta Crystallographica Section E Crystallographic Communications 74, no. 10 (2018): 1491–96. http://dx.doi.org/10.1107/s2056989018013087.

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The crystal structures of (E)-1-(anthracen-9-yl)-3-(3H-indol-2-yl)prop-2-en-1-one, C25H17NO, and (E)-1-(anthracen-9-yl)-3-[4-(dimethylamino)naphthalen-1-yl]prop-2-en-1-one, C29H23NO, are reported. In each case the anthracene ring system and pendant ring system are almost perpendicular to each other [dihedral angles = 75.57 (7)° and 70.26 (10)°, respectively]. In the extended structures, weak N—H...O, C—H...O and C—H...π interactions influence the centrosymmetric crystal packing. Density functional theory calculations were carried out using a 6–311 G++(d,p) basis set and the calculated structur

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9

Liao, Chung-Ping, Otto Phanstiel, Mark E. Lasbury, et al. "Polyamine Transport as a Target for Treatment of Pneumocystis Pneumonia." Antimicrobial Agents and Chemotherapy 53, no. 12 (2009): 5259–64. http://dx.doi.org/10.1128/aac.00662-09.

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ABSTRACT Polyamine levels are greatly increased in alveolar macrophages (AMs) during Pneumocystis pneumonia (PCP), leading to increased production of H2O2, which causes AMs to undergo apoptosis. One of the mechanisms by which polyamine levels in AMs are elevated is enhanced uptake of exogenous polyamines. In this study, the possibility of targeting polyamine uptake as a treatment for PCP was examined. Four anthracene- and one benzene-polyamine conjugates that are potential polyamine transport inhibitors, including N1-anthracen-9-ylmethyl-butane-1,4-diamine; N-(4-aminobutyl)-N-anthracen-9-ylmet

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10

Lee, Jaehyun, Seungho Kim, Jee-Hwan Kim, and Jongwook Park. "A New Anthracene Derivative Containing t-Butyl Group for Solution Process Organic Light-Emitting Diodes." Journal of Nanoscience and Nanotechnology 15, no. 10 (2015): 8285–88. http://dx.doi.org/10.1166/jnn.2015.11258.

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4-(10-(3′,5′-diphenylbiphenyl-4-yl)anthracen-9-yl)-N,N-diphenylaniline [TATa] and a new anthracene derivative of 4-(2 or 3-tert-butyl-10-(3′,5′-diphenylbiphenyl-4-yl)anthracen-9-yl)-N,N-diphenylaniline [T-TATa] isomer by introduced t-butyl group were synthesized. OLED devices of TATa and T-TATa were fabricated by solution process. Its physical properties such as optical, electrochemical, and electroluminescent properties were also investigated. Two compounds were used as emitting layer (EML) in OLED device: ITO/PEDOT (40 nm)/synthesized materials (60 nm)/TPBi (20 nm)/LiF (1 nm)/Al (200 nm). Th

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11

Zainuri, Dian Alwani, Ibrahim Abdul Razak, and Suhana Arshad. "Crystal structure, spectroscopic characterization and DFT study of two new linear fused-ring chalcones." Acta Crystallographica Section E Crystallographic Communications 74, no. 10 (2018): 1427–32. http://dx.doi.org/10.1107/s2056989018012641.

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The structures of two new anthracenyl chalcones, namely (E)-1-(anthracen-9-yl)-3-(4-nitrophenyl)prop-2-en-1-one, C23H15NO3, and (E)-1-(anthracen-9-yl)-3-(4-iodophenyl)prop-2-en-1-one, C23H15IO are reported. A structural comparative study between the two chalcones was performed and some effects on the geometrical parameters, such as planarity and dihedral angles, are described. The molecular geometry was determined by single-crystal X-ray diffraction, and density functional theory (DFT) at B3LYP with the 6–311++G(d,p) basis set was applied to optimize the ground-state geometry. In addition, int

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12

Janovec, Ladislav, Stanislav Böhm, Ivan Danihel, Ján Imrich, Pavol Kristian, and Karel D. Klika. "Theoretical Confirmation of the Reaction Mechanism Leading to Regioselective Formation of Thiazolidin-4-one from Bromoacetic Acid Derivatives." Collection of Czechoslovak Chemical Communications 72, no. 10 (2007): 1435–45. http://dx.doi.org/10.1135/cccc20071435.

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A regioselective synthesis of 3-alkyl-2-[(anthracen-9-yl)imino]thiazolidin-4-ones 2a-2e and 2-(alkylimino)-3-(anthracen-9-yl)thiazolidin-4-ones 3a-3e from appropriate thioureas using methyl bromoacetate or bromoacetyl bromide, respectively, has been rationalized by DFT calculations of model thiourea and its phenyl derivative. The proposed mechanism indicates that the regioselective formation of the target thiazolidinones is a consequence of a different reactivity of the reagents and a varying stability of the intermediates, 1-alkyl-3-(anthracen-9-yl)-2-[(methoxycarbonyl)methyl]isothioureas 4a-

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13

Kumar, Harish, Sandeep Jain, and Neelam Jain. "Synthesis and antibacterial activity of some 3-(5-aryl-4H-pyrazol-3-yl) anthracen-10(9H)-ones." Indian Journal of Pharmaceutical and Biological Research 2, no. 03 (2014): 12–17. http://dx.doi.org/10.30750/ijpbr.2.3.3.

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A series of 3-(5-aryl-4H-pyrazol-3-yl)anthracen-10(9H)-ones were synthesized from anthracen-10(9H)-one (1) and studied for their in vitro antibacterial activity. Anthracen- 10(9H)-one after Friedel crafts acetylation with acetyl chloride yielded 3-acetylanthracen- 10(9H)-one (2) which on further reaction with substituted aromatic aldehydes in the presence of catalytic amount of sodium hydroxide in water and ethanol furnished the corresponding 3-(3-arylacryloyl)anthracen-10(9H)-ones (3a-g) as intermediate compounds, which on further reaction with hydrazine hydrate in absolute ethanol formed the

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14

Teki, Yoshio, Sadaharu Miyamoto та Kentaro Koide. "π-Topology and spin alignment in the photo-excited states of phenylanthracene-t-butylnitroxide radicals". Physical Chemistry Chemical Physics 17, № 47 (2015): 31646–52. http://dx.doi.org/10.1039/c5cp05994a.

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We have studied the relationship between the π-topology and the photo-excited high-spin states of π-conjugated spin systems, 9-anthracen-(3-phenyl-t-butylnitroxide) radical (1m) and 9-anthracen-(4-phenyl-t-butylnitroxide) radical (1p) systems, by time-resolved ESR and transient absorption spectroscopies.

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15

Rozek, Tomas, Tomas Rozek, Dennis K. Taylor, et al. "Syntheses of Angucyclinones Related to Ochromycinone. III. An 11-Hydroxy Isomer and Some Reduced Analogues." Australian Journal of Chemistry 52, no. 2 (1999): 129. http://dx.doi.org/10.1071/c98124.

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The boron triacetate assisted Diels Alder reaction between racemic 5,5-dimethyl-3-vinylcyclohex- 2-enyl acetate and 5-hydroxynaphthoquinone yields the racemic 11-hydroxy-3,3-dimethyl-7,12-dioxo- 1,2,3,4,6,6a,7,12,12a,12b-decahydrobenzo[a]anthracen-1-yl acetate as the sole stereoisomer by regio- and stereo-selective cis endo addition. Aromatization of the Diels Alder adduct followed by hydrolysis of the acetate and oxidation of the resultant 1-hydroxy group gives the target angucyclinone, 11-hydroxy-3,3-dimethyl-1,2,3,4,7,12-hexahydrobenzo[a]anthracene-1,7,12-trione, in an overall yield of 37%

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16

Pathak, Dinesh, Sanjay Kumar, Sonali Andotra, et al. "New tailored organic semiconductors thin films for optoelectronic applications." European Physical Journal Applied Physics 95, no. 1 (2021): 10201. http://dx.doi.org/10.1051/epjap/2021210090.

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In this study, we have investigated new tailored organic semiconductor materials for optoelectronic application, such as organic solar cells. The carbon-based organic semiconductor material has promising advantages in organic thin-film form. Moreover, due to its low cost, organic thin films are suitable and cheaper than inorganic thin-film. The bandgap of organic semiconductors materials can be tuned and mostly lies between 2.0 eV and 4 eV and the optical absorption edge of organic semiconductors typically lies in between 1.7 eV and 3 eV. They can be easily tailored by modifying the carbon cha

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17

Petek, Hande, Şamil Işık, Nesuhi Akdemir, Cihan Kantar, Erbil Ağar, and İsmet Şenel. "4-(Anthracen-9-ylmethoxy)phthalonitrile." Acta Crystallographica Section E Structure Reports Online 60, no. 2 (2004): o256—o257. http://dx.doi.org/10.1107/s1600536804000285.

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18

Elazami, M., N. Bitit, A. Kerbal, M. Fahim, B. El-Bali, and M. Bolte. "Diethyl 2-anthracen-9-ylmethylenemalonate." Acta Crystallographica Section C Crystal Structure Communications 55, no. 4 (1999): IUC9900037. http://dx.doi.org/10.1107/s0108270199099643.

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19

Han, Jian-Rong, Wei Wang, Xiao-Li Zhen, Xia Tian, and Shou-Xin Liu. "(Anthracen-9-ylmethyl)benzylammonium chloride." Acta Crystallographica Section E Structure Reports Online 67, no. 6 (2011): o1482. http://dx.doi.org/10.1107/s1600536811016837.

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20

Dinh, Thi Hien, and Minh Hai Nguyen. "Structure and luminescent property of a Sm3+ complex containing benzoyltrifluoroacetone and 1,2-bis[(anthracen-9-ylmethyl)amino]ethane ligands." Ministry of Science and Technology, Vietnam 63, no. 2 (2021): 20–24. http://dx.doi.org/10.31276/vjste.63(2).20-24.

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The synthesis, structure, and luminescent propertiesof a samarium(III) complex (A2) containing benzoyltrifluoroacetone (HTFPB) and 1,2-bis[(anthracen-9-ylmethyl)amino]ethane (BAAE2) ligands are herein reported. The structure of A2 has been elucidated by infrared spectroscopy and single crystal X-ray diffraction. X-ray crystallographic analysis demonstrated that A2 has a mononuclear structure with a formula of Sm(TFPB)3(BAAE2) in which Sm3+ ion is coordinated to six O-atoms from three TFPB ligands and two N-atoms from one ancillary ligand (BAAE2). UV-Vis data show that A2 strongly absorbs in th

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21

Kiwada, Tatsuto, Hiroshi Takayama, Aika Hirasaki, Kazuma Ogawa, and Akira Odani. "Asymmetric structure of cis-[N-(9-anthracenylmethyl)-1,2-ethanediamine]dipyridineplatinum(II) dinitrate." Acta Crystallographica Section C Structural Chemistry 73, no. 11 (2017): 975–78. http://dx.doi.org/10.1107/s2053229617014255.

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Platinum antitumour agents, containing aromatic rings, which are used for targeting DNA in effective therapies for the treatment of cancer. We have synthesized the title metallocomplex with an aromatic ligand and determined its crystal structure. In many cases, complexes of platinum and other metals have a symmetrical structure. In contrast, the platinum(II) complex with pyridine and N-(9-anthracenylmethyl)-1,2-ethanediamine as ligands (systematic name: cis-{N-[(anthracen-9-yl)methyl]ethane-1,2-diamine-κ2 N,N′}bis(pyridine-κN)platinum(II) dinitrate), [Pt(C5H5N)2(C17H18N2)](NO3)2, is asymmetric

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22

Rybalko, Majya V., Anna A. Shmygareva, and Anatoly N. Sankov. "Development of the method of quantitative determination of anthracen derivatives in rhizomes and roots of Rubia tinctorum." Aspirantskiy Vestnik Povolzhiya 19, no. 5-6 (2020): 143–47. http://dx.doi.org/10.17816/2072-2354.2019.19.3.143-147.

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This paper discusses the current methods to improve standardization procedure of medicinal plant raw materials of Rubia tinctorum. New approaches for quantitative analysis of rhizomes and roots of Rubia tinctorum are introduced. They include spectrophotometry at the analytical wavelength of 510 nm and ultrasound. These methods helped to achieve the maximal output of anthracen derivatives from raw materials. At present, existing technology for extracting medicinal substances from animal and plant tissues is mostly inefficient and time-consuming. Low-frequency ultrasound reduces the time of extr

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23

Klaper, Matthias, and Torsten Linker. "Hinweise auf einen Sauerstoff-Anthracen-Sandwichkomplex." Angewandte Chemie 125, no. 45 (2013): 12112–15. http://dx.doi.org/10.1002/ange.201304768.

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24

Li, Ruohan, Shuzhang Xiao, Yi Li, et al. "Polymorphism-dependent and piezochromic luminescence based on molecular packing of a conjugated molecule." Chem. Sci. 5, no. 10 (2014): 3922–28. http://dx.doi.org/10.1039/c4sc01243g.

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25

Liu, Jialei, Fuyang Huo, and Wenqing He. "Construction of a simple crosslinking system and its influence on the poling efficiency and oriental stability of organic electro-optic materials." RSC Advances 10, no. 11 (2020): 6482–90. http://dx.doi.org/10.1039/c9ra10813k.

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26

Chen, You, Hui Peng, Yun-Xiao Pi, et al. "Efficient phosphine ligands for the one-pot palladium-catalyzed borylation/Suzuki–Miyaura cross-coupling reaction." Organic & Biomolecular Chemistry 13, no. 11 (2015): 3236–42. http://dx.doi.org/10.1039/c4ob02436b.

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27

Dekic, Stojadin, Vidoslav Dekic, Branimirka Vucic, Biljana Dekic, and Milan Dekic. "Synthesis of new condensed coumarin derivatives." Facta universitatis - series: Physics, Chemistry and Technology 5, no. 1 (2007): 85–88. http://dx.doi.org/10.2298/fupct0701085d.

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Reactions of 4-chloro-2-oxo-2H-chromene-3-carbonitrile (1) with 4-methylpyridin- 2-ylamine (2) and 6-methoxy-benzothiazol-2-ylamine (3) in acetonitrile containing a catalytic amount of triethylamine gave the new coumarin derivatives 7-imino-10-methyl-7H- 5-oxa-7a,12-diaza-benzo[a]anthracen-6-one (4) and 7-imino-10-methoxy-7H-5-oxa-12- thia-7a,13-diaza-indeno[1,2-b]phenanthren-6-one (5) in 52 and 39% yields, respectively. The novel compounds were subjected to acid hydrolysis giving the corresponding oxoderivatives 10-methyl-5-oxa-7a,12-diaza-benzo[a]anthracene-6,7-dione (6) and 10- methoxy-5-ox

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28

Tong, Fei, Maram Al-Haidar, Lingyan Zhu, Rabih O. Al-Kaysi, and Christopher J. Bardeen. "Photoinduced peeling of molecular crystals." Chemical Communications 55, no. 26 (2019): 3709–12. http://dx.doi.org/10.1039/c8cc10051a.

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29

Klein, Hans-Friedrich, Klaus Ellrich, Susanne Lamac, Goetz Lull, Laszlo Zsolnai, and Gottfried Hüttner. "Anthracen- und Phenanthren-Cobalt-Verbindungen mit Trimethylphosphan-Liganden / Anthracene and Phenanthrene Cobalt Compounds Containing Trimethylphosphane Ligands." Zeitschrift für Naturforschung B 40, no. 10 (1985): 1377–82. http://dx.doi.org/10.1515/znb-1985-1023.

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Anthracene and phenanthrene complexes of zerovalent cobalt, Co(Cl4H10)(PMe3)3, are obtained by substitution of olefin in Co(olefin)(PMe3)3 (olefin = propene, cyclopentene). Ethene replaces the η2-bonded aromatic molecules. Substitution labile ligands L′ in hydridocobalt complexes CoH(L′)(PMe3)3 (L′ = N2, C4H8) give way to an anthracene or phenanthrene ligand and can in turn be replaced by carbon monoxide. η4-Coordinated anthracene in Co[Sn(C6H5)3](C14H10)(PMe3)2 is not replaced by CO under normal conditions. In η2-coordinated anthracene the bond between coordinated C-atoms in ring positions 2

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30

Gribble, Gordon W., Craig S. LeHoullier, Mukund P. Sibi, and Robert W. Allen. "Synthesis and deamination of 7,12-dihydrobenz[a]anthracen-7,12-imines. A new benz[a]anthracene synthesis." Journal of Organic Chemistry 50, no. 10 (1985): 1611–16. http://dx.doi.org/10.1021/jo00210a011.

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31

Vaisburg, A. F., N. M�ller, and H. Falk. "2-(10-Diazo-10H-anthracen-9-ylidene)-malonodinitrile: A convenient precursor of 9,10-disubstituted anthracenes." Monatshefte f�r Chemie Chemical Monthly 126, no. 6-7 (1995): 773–81. http://dx.doi.org/10.1007/bf00807169.

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32

Almansour, Abdulrahman I., Natarajan Arumugam, Raju Suresh Kumar, P. Vijayalakshmi, and J. Suresh. "9-(2-Chlorobenzylidene)anthracen-10(9H)-one." Acta Crystallographica Section E Structure Reports Online 69, no. 5 (2013): o627. http://dx.doi.org/10.1107/s160053681300809x.

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33

Howie, R. Alan, and Solange M. S. V. Wardell. "(Anthracen-9-ylmethyl)dimethylamine at 120 K." Acta Crystallographica Section E Structure Reports Online 61, no. 6 (2005): o1686—o1688. http://dx.doi.org/10.1107/s1600536805014200.

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34

Hu, Hua-You, Yu-Cheng Huang, Hai-Tao Yu, and Yan Zhang. "(Anthracen-9-yl)(piperidin-1-yl)methanone." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2120. http://dx.doi.org/10.1107/s1600536808033205.

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35

Geetha, K., D. K. Andrew Prasanna Kumar, D. Lakshmanan, R. Savitha, and S. Murugavel. "(E)-N-(Anthracen-9-ylmethylidene)-4-nitroaniline." Acta Crystallographica Section E Structure Reports Online 67, no. 10 (2011): o2577. http://dx.doi.org/10.1107/s1600536811035859.

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36

Jira, Thomas, and Christof Tröltzsch. "Flüssigehromatographische Trennung von Anthracen und seinen Hydrierprodukten." Zeitschrift für Chemie 23, no. 9 (2010): 341–42. http://dx.doi.org/10.1002/zfch.19830230915.

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37

Fan, Wei-Qiang, and Fu-Xiao Chen. "N-(Anthracen-9-ylmethyl)adamantan-1-amine." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1831. http://dx.doi.org/10.1107/s1600536812022106.

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38

Howie, R. Alan, Andrew Kindness, Michael G. McKay, and Glenn E. M. Maguire. "(Anthracen-9-ylmethyl)diethylamine at 100 K." Acta Crystallographica Section E Structure Reports Online 61, no. 1 (2004): o52—o54. http://dx.doi.org/10.1107/s1600536804031265.

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39

Liu, Qing-Xiang, Hai-Bin Song, and Zheng-Ming Li. "N,N-Bis(anthracen-9-ylmethyl)propylamine." Acta Crystallographica Section E Structure Reports Online 61, no. 2 (2005): o385—o386. http://dx.doi.org/10.1107/s1600536804034026.

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40

Khorasani, Sanaz, and Manuel A. Fernandes. "1-(Anthracen-1-yl)pyrrolidine-2,5-dione." Acta Crystallographica Section E Structure Reports Online 68, no. 5 (2012): o1503. http://dx.doi.org/10.1107/s160053681201536x.

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41

Almansour, Abdulrahman I., Natarajan Arumugam, Usama Karama, Ibrahim Abdul Razak, and Suhana Arshad. "10-(4-Methylbenzylidene)anthracen-9(10H)-one." Acta Crystallographica Section E Structure Reports Online 68, no. 2 (2012): o478—o479. http://dx.doi.org/10.1107/s1600536812000827.

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42

Nagarajan, Kalaivanan, Shinaj K. Rajagopal та Mahesh Hariharan. "C–H⋯H–C and C–H⋯π contacts aid transformation of dimeric to monomeric anthracene in the solid state". CrystEngComm 16, № 38 (2014): 8946–49. http://dx.doi.org/10.1039/c4ce01278j.

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43

JOHNSON, REEJA, JOBY THOMAS KAKKASSERY, Vinod Raphael Palayoor, Ragi Kooliyat, and Vidhya Thomas Kannanaikkal. "Experimental and Theoretical Investigations on the Corrosion Inhibition action of Thiadiazole Derivatives on Carbon Steel in 1M HCl medium." Oriental Journal Of Chemistry 36, no. 6 (2020): 1179–88. http://dx.doi.org/10.13005/ojc/360624.

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Abstract:

Novel thiadiazole derivatives of Schiff bases namely (E)-N-(anthracen-9-ylmethylene)-5-(4-nitrophenyl)-1,3,4-thiadiazol-2-amine (A9CNPTDA) and N-(anthracen-9(10H)-ylidene)-5-(4-nitrophenyl)-1,3,4-thiadiazol-2-amine (ANNPTDA) were synthesized, characterized and corrosion inhibition behaviour, as well as the mechanism of inhibition were investigated by different monitoring techniques like gravimetric measurements, electrochemical impedance spectroscopy, potentiodynamic polarization, quantum chemical and SEM studies. Both of the thiadiazole derivatives showed excellent corrosion inhibitor action

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44

Shih, Ke-Ying, Yung-Chih Lin, Tai-Shen Hsiao, Shiang-Lin Deng, Shiao-Wei Kuo, and Jin-Long Hong. "Amorphous and crystalline blends from polytyrosine and pyridine-functionalized anthracene: hydrogen-bond interactions, conformations, intramolecular charge transfer and aggregation-induced emission." Polym. Chem. 5, no. 19 (2014): 5765–74. http://dx.doi.org/10.1039/c4py00706a.

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A new pyridine-terminated fluorophore of (E)-4-(2-(anthracen-9-yl)vinyl)pyridine (AnPy) with intramolecular charge transfer and aggregation-induced emission properties was synthesized and was blended with polytyrosine (PTyr) through hydrogen-bond interactions.

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45

Xu, Li, Peng-Fei Wang, Juan-Juan Zhang, et al. "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

Asiri, Abdullah M., and Salman A. Khan. "Anthracen-9-ylmethylene-(3,4-dimethylisoxazol-5-yl)amine." Molbank 2011, no. 3 (2011): M736. http://dx.doi.org/10.3390/m736.

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47

Heuer, Lutz, Dietmar Schomburg, and Reinhard Schmutzler. "Dimeres 9-(Difluorphosphino)anthracen: Synthese, Eigenschaften und Struktur." Chemische Berichte 122, no. 8 (1989): 1473–76. http://dx.doi.org/10.1002/cber.19891220815.

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48

Taylor, Peter N, Andrew P Wylie, Juhani Huuskonen, and Harry L Anderson. "Verstärkte elektronische Konjugation in Porphyrin-Anthracen-Porphyrin-Ketten." Angewandte Chemie 110, no. 7 (1998): 1033–37. http://dx.doi.org/10.1002/(sici)1521-3757(19980403)110:7<1033::aid-ange1033>3.0.co;2-w.

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49

Palani, K., P. Amaladass, A. K. Mohanakrishnan, and M. N. Ponnuswamy. "3-(Anthracen-9-yl)-3H-isobenzofuran-1-one." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (2005): o55—o57. http://dx.doi.org/10.1107/s1600536805039553.

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50

Zhao, Meng, Gang Zhang, Jingmiao Zhang, Shan Huang, Xiuxia Liu, and Fei Li. "Crystal structure of 4-(anthracen-9-yl)pyridine." Acta Crystallographica Section E Crystallographic Communications 77, no. 6 (2021): 605–8. http://dx.doi.org/10.1107/s2056989021004710.

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The title compound, C19H13N, which crystallizes in the monoclinic C2/c space group with one half-molecule in the asymmetric unit, was synthesized by Suzuki–Miyaura cross-coupling reaction of 9-bromoanthracene with pyridin-4-ylboronic acid and purified by column chromatography on silica gel. Light-yellow crystals of 4-(anthracen-9-yl)-pyridine suitable for X-ray diffraction were collected by the solvent evaporation method. In the crystal, pairs of molecules are connected by intermolecular C—H...π (pyridine) interactions [d(H7...Cg) = 2.7391 (2) Å], forming cyclic centrosymmetric dimers, further

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