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Journal articles on the topic 'Heteroaromatic rings'

Author: Grafiati

Published: 1 April 2023

Last updated: 31 July 2025

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1

Pitt, William R., David M. Parry, Benjamin G. Perry, and Colin R. Groom. "Heteroaromatic Rings of the Future." Journal of Medicinal Chemistry 52, no. 9 (2009): 2952–63. http://dx.doi.org/10.1021/jm801513z.

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2

Doerksen, Robert J., and Ajit J. Thakkar. "Bond orders in heteroaromatic rings." International Journal of Quantum Chemistry 90, no. 2 (2002): 534–40. http://dx.doi.org/10.1002/qua.998.

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3

Orita, Akihiro, Fangguo Ye, Govindarajulu Babu, Tomohiro Ikemoto, and Junzo Otera. "Double elimination protocol for the synthesis of arylene ethynylenes containing heteroaromatic rings." Canadian Journal of Chemistry 83, no. 6-7 (2005): 716–27. http://dx.doi.org/10.1139/v05-038.

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The double elimination reaction of β-substituted sulfones offers a versatile strategy for synthesis of arylene ethynylene kits containing heteroaromatic rings. A sequence of aldol reaction between α-sulfonyl carbanion and aldehyde, trapping the resulting aldolate to give β-substituted sulfone, and double elimination of this intermediate can be integrated in one pot. This protocol allows thiophene, pyridine, and ferrocene units to be accommodated in phenylene ethynylene arrays.Key words: aryleneethynylenes, heteroaromatic rings, ferrocene, double elimination, sulfones.

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4

Landmana, Marilé, Helmar Görls, Chantelle Crause, Hubert Nienaber, Andrew Olivier, and Simon Lotz. "Di-tungsten Bis-carbene Complexes Linked by Condensed Heteroaromatic Spacers." Zeitschrift für Naturforschung B 62, no. 3 (2007): 419–26. http://dx.doi.org/10.1515/znb-2007-0316.

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The 2,7-dilithiated substrates of 3,6-dimethylthieno[3,2-b]thiophene, N,N′-dimethylpyrrolo[3,2- b]pyrrole and N-methylthieno[3,2-b]pyrrole were reacted with W(CO)6 to give, after subsequent alkylation with Et3OBF4, the ditungsten biscarbene complexes [(CO)5W{C(OEt)XXC(OEt)} W(CO)5] (XX = condensed heteroaromatic spacers). Sites of attack during the dilithiation of the condensed rings were studied and compared, and the yields of the desired ditungsten biscarbene complexes optimized by changing the reaction conditions according to the role of the heteroatoms in the rings. The crystallographic da

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5

Mitsunuma, Harunobu, Hiromu Fuse, Yu Irie, et al. "(Invited) Identification of a Self-Photosensitizing Hydrogen Atom Transfer Organocatalyst System." ECS Meeting Abstracts MA2023-01, no. 14 (2023): 1355. http://dx.doi.org/10.1149/ma2023-01141355mtgabs.

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The carbon-hydrogen (C-H) bond is a fundamental chemical bond that constitutes organic molecules, and its direct conversion leads to highly efficient molecular synthesis. In recent years, the hydrogen atom transfer (HAT) catalysis using the energy of visible light, has been attracting attention. However, existing methods require the use of photoredox catalysts such as organic molecules with complex structures and expensive metal complexes. In this study, we developed an organocatalytic system that mimics the electron transfer process of enzymes in vivo and promotes functionalization of stable

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6

Meena, Chhuttan L., Shubdha Ingole, Satyendra Rajpoot, et al. "Discovery of a low affinity thyrotropin-releasing hormone (TRH)-like peptide that exhibits potent inhibition of scopolamine-induced memory impairment in mice." RSC Advances 5, no. 70 (2015): 56872–84. http://dx.doi.org/10.1039/c5ra06935a.

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7

Doerksen, Robert J., and Ajit J. Thakkar. "Quadrupole and Octopole Moments of Heteroaromatic Rings." Journal of Physical Chemistry A 103, no. 48 (1999): 10009–14. http://dx.doi.org/10.1021/jp992524v.

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8

Gamez, Patrick, Tiddo J. Mooibroek, Simon J. Teat та Jan Reedijk. "Anion Binding Involving π-Acidic Heteroaromatic Rings". Accounts of Chemical Research 40, № 6 (2007): 435–44. http://dx.doi.org/10.1021/ar7000099.

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9

Katritzky, Alan R., and Nicholas Dennis. "Cycloaddition reactions of heteroaromatic six-membered rings." Chemical Reviews 89, no. 4 (1989): 827–61. http://dx.doi.org/10.1021/cr00094a006.

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10

Thorimbert, Serge, Candice Botuha, and Kevin Passador. "‘Heteroaromatic Rings of the Future’: Exploration of Unconquered Chemical Space." Synthesis 51, no. 02 (2018): 384–98. http://dx.doi.org/10.1055/s-0037-1611279.

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William Pitt and co-workers have created a virtual exploratory heterocyclic library ‘VEHICLe’ containing over 200 unconquered bicyclic heteroaromatic rings, synthetically feasible with potential medicinal interest. Since the publication of the 22 ‘heteroaromatic rings of the future’ by Pitt in 2009, 15 of them have been successfully synthesized as bicyclic or polycyclic forms and evaluated for applications in both biology and material science. This short review presents the critical synthesis associated with innovative synthetic methodologies of the synthetically conquered ring scaffolds from

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11

Silva Júnior, P. E., L. C. D. Rezende, Julia Possamai Gimenes, et al. "Synthesis of two ‘heteroaromatic rings of the future’ for applications in medicinal chemistry." RSC Advances 6, no. 27 (2016): 22777–80. http://dx.doi.org/10.1039/c6ra01099g.

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12

Khazaei, Ardeshir, Mohammad Ali Zolfigol, Mohmmad Mokhlesi, and Mahtab Pirveysian. "Citric acid as a trifunctional organocatalyst for thiocyanation of aromatic and heteroaromatic compounds in aqueous media." Canadian Journal of Chemistry 90, no. 5 (2012): 427–32. http://dx.doi.org/10.1139/v2012-013.

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A green and simple procedure for the thiocynation of aromatic and heteroaromatic rings in the presence of a catalytic amount of citric acid in water are described. The reactions proceed in high yields, with short reaction times and under mild conditions.

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13

Angelini, Giancarlo, Cinzia Sparapani, and Maurizio Speranza. "Gas-phase heteroaromatic substitution. 7. Methylation of five-membered heteroaromatic rings by free methyl cations." Journal of the American Chemical Society 112, no. 8 (1990): 3060–63. http://dx.doi.org/10.1021/ja00164a028.

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14

Crestoni, Maria Elisa, Simonetta Fornarini, and Maurizio Speranza. "Gas-phase heteroaromatic substitution. 9. Silylation of simple five-membered heteroaromatic rings by trimethylsilyl cations." Journal of the American Chemical Society 112, no. 19 (1990): 6929–35. http://dx.doi.org/10.1021/ja00175a029.

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15

Lipshutz, Bruce H. "Five-membered heteroaromatic rings as intermediates in organic synthesis." Chemical Reviews 86, no. 5 (1986): 795–819. http://dx.doi.org/10.1021/cr00075a005.

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16

Seo, Jia, Che-Wei Chen, Shih-Ching Chuang, et al. "Palladium-Catalyzed C–H Benzannulation of Functionalized Furans and Pyrroles with Alkynes." Synthesis 53, no. 17 (2021): 3001–10. http://dx.doi.org/10.1055/a-1502-3641.

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AbstractA benzannulation strategy involving activation of two C–H bonds of five-membered heteroarenes was developed. Readily available furans and pyrroles stabilized by synthetically useful electron-withdrawing groups underwent Pd-catalyzed 1:2 annulation reactions with diaryl alkynes. A variety of functional groups, including ester, amide, ketone, aldehyde, and nitrile, on the heterocyclic cores were tolerated in the Pd-catalyzed oxidative reactions. In these reactions, the combination of 2,2-dimethylbutyric acid and its conjugate base facilitated metalation at the heteroaromatic rings and re

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17

Kondratov, Ivan S., Oleksandr O. Grygorenko, Oleksandr O. Stepaniuk та ін. "Synthesis of Fused Pyridine Carboxylates by Reaction of β-Alkoxyvinyl Glyoxylates with Amino Heterocycles". Synthesis 52, № 13 (2020): 1915–26. http://dx.doi.org/10.1055/s-0039-1707987.

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An efficient approach to the preparation of pyridine carboxylates fused with 5- or 6-membered heteroaromatic rings is described. The method relied on the Combes-type condensation of the low-molecular-weight β-alkoxyvinyl glyoxylates as CCC bis-electrophiles and with heteroaromatic amines as NCC binucleophiles. In most experiments, β-alkoxyvinyl glyoxylates without additional substituent at the β position led to the corresponding α-pyridine carboxylates (67–87% yield). In the case of β-methyl-substituted derivative, γ-pyridine carboxylates were obtained in 84–99% yield. It was found that regi

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18

Lattelais, M., Y. Ellinger, A. Matrane, and J. C. Guillemin. "Looking for heteroaromatic rings and related isomers as interstellar candidates." Physical Chemistry Chemical Physics 12, no. 16 (2010): 4165. http://dx.doi.org/10.1039/b924574j.

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19

Bejan, Andrei, Dragos Peptanariu, Bogdan Chiricuta, Elena Bicu, and Dalila Belei. "Low Molecular Weight Microfibers with Light Sensing Properties." Materiale Plastice 54, no. 4 (2017): 655–58. http://dx.doi.org/10.37358/mp.17.4.4920.

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Microfibers were obtained from organic low molecular weight compounds based on heteroaromatic and aromatic rings connected by aliphatic spacers. The obtaining of microfibers was proved by scanning electron microscopy. The deciphering of the mechanism of microfiber formation has been elucidated by X-ray diffraction, infrared spectroscopy, and atomic force microscopy measurements. By exciting with light of different wavelength, florescence microscopy revealed a specific optical response, recommending these materials for light sensing applications.

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20

Zhou, Chun-Shan, Ya-Mei Pei, and Xiang-Gao Meng. "2,2′,2′′,2′′′-(3,6-Dioxaoctane-1,8-diyldinitrilo)tetrabenzimidazolium tetrakis(perchlorate) dihydrate." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4334—o4335. http://dx.doi.org/10.1107/s160053680704980x.

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In the title crystal structure, C38H44N10O2 4+·4ClO4 −·2H2O, components are linked into a two-dimensional framework by a combination of N—H...O, C—H...O, O—H...O and N—H...N hydrogen bonds. In addition, weak π–π stacking interactions and anion–π noncovalent interactions between perchlorate anions and heteroaromatic imidazole rings [O...Cg = 3.328 (10) and 3.386 (11) Å; Cg is the centroid of an imidazole ring] consolidate the crystal structure.

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21

Grenet, Erwann, Ashis Das, Paola Caramenti, and Jérôme Waser. "Rhodium-catalyzed C–H functionalization of heteroarenes using indoleBX hypervalent iodine reagents." Beilstein Journal of Organic Chemistry 14 (May 25, 2018): 1208–14. http://dx.doi.org/10.3762/bjoc.14.102.

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The C–H indolation of heteroarenes was realized using the benziodoxolone hypervalent iodine reagents indoleBXs. Functionalization of the C–H bond in bipyridinones and quinoline N-oxides catalyzed by a rhodium complex allowed to incorporate indole rings into aza-heteroaromatic compounds. These new transformations displayed complete regioselectivity for the C-6 position of bipyridinones and the C-8 position of quinoline N-oxides and tolerated a broad range of functionalities, such as halogens, ethers, or trifluoromethyl groups.

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22

Harada, Shinji, Daiki Matsuda, Takahiro Morikawa, and Atsushi Nishida. "Direct Synthesis of Enones by Visible-Light-Promoted Oxygenation of Trisubstituted Olefins Using Molecular Oxygen." Synlett 31, no. 14 (2020): 1372–77. http://dx.doi.org/10.1055/s-0040-1707150.

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A one-step synthesis of enones from olefins is described. The reaction was performed under visible-light irradiation in the presence of molecular oxygen and a photocatalyst. The reaction proceeded with various types of trisubstituted olefins to give enones in good yields with high regioselectivity. In particular, oxygen- and nitrogen-containing functional groups, heteroaromatic rings, and cyclopropanes were tolerated. Mechanistic studies and previous reports indicated that the active oxygen species generated in the reaction system is singlet oxygen.

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23

Cooper, David L., Stuart C. Wright, Joseph Gerratt, and Mario Raimondi. "The electronic structure of heteroaromatic molecules. Part 1. Six-membered rings." Journal of the Chemical Society, Perkin Transactions 2, no. 3 (1989): 255. http://dx.doi.org/10.1039/p29890000255.

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24

Cooper, David L., Stuart C. Wright, Joseph Gerratt, and Mario Raimondi. "The electronic structure of heteroaromatic molecules. Part 2. Five-membered rings." Journal of the Chemical Society, Perkin Transactions 2, no. 3 (1989): 263. http://dx.doi.org/10.1039/p29890000263.

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25

McKay, Sonya L., Brandy Haptonstall, and Samuel H. Gellman. "Beyond the Hydrophobic Effect: Attractions Involving Heteroaromatic Rings in Aqueous Solution1." Journal of the American Chemical Society 123, no. 6 (2001): 1244–45. http://dx.doi.org/10.1021/ja003256d.

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26

Fraser, Robert R., Tarek S. Mansour, and Sylvain Savard. "Acidity measurements in THF. V. Heteroaromatic compounds containing 5-membered rings." Canadian Journal of Chemistry 63, no. 12 (1985): 3505–9. http://dx.doi.org/10.1139/v85-574.

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The pKa's of 13 heterocyclic aromatic compounds have been measured in tetrahydrofuran (THF) using 13C nmr spectroscopy. The acidifying effect of a nitrogen heteroatom is seen to be quite large (4–6 pK units versus C—H) on an adjacent C—H bond but small on a more remote hydrogen. Most of these aromatic heterocycles are sufficiently acidic, pKa < 34, to be completely deprotonated by lithium tetramethylpiperidide in THF. Benzoxazole appears to be an extremely strong carbon acid, its ring-opened isomer having a pKa of less than 15.7.

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27

Ferreiro, Juan J., Jose G. de la Campa, Angel E. Lozano, and Javier de Abajo. "Polyisophthalamides with heteroaromatic pendent rings: Synthesis, physical properties, and water uptake." Journal of Polymer Science Part A: Polymer Chemistry 43, no. 21 (2005): 5300–5311. http://dx.doi.org/10.1002/pola.21000.

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28

Cui, Yongkang, Shoufei Cheng, Lin Ling, Yuxue Li, and Long Lu. "Theoretical Study on Energetic Materials Containing (Difluoramino)dinitromethyl Substituted Heteroaromatic Rings." Acta Chimica Sinica 82, no. 4 (2024): 377. http://dx.doi.org/10.6023/a24010017.

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29

Chmovzh, Timofey N., Timofey A. Kudryashev, and Oleg A. Rakitin. "4,7-Bis(dodecylthio)-[1,2,5]thiadiazolo[3,4-c]pyridine." Molbank 2021, no. 4 (2021): M1291. http://dx.doi.org/10.3390/m1291.

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Bis(alkylsulfanyl) derivatives of 1,2,5-thiadiazoles fused with aromatic and heteroaromatic rings containing long alkyl chains are of interest as compounds with liquid crystalline properties. In this communication, 4,7-bis(dodecylthio)-[1,2,5]thiadiazolo[3,4-c]pyridine 1 was obtained from 4,7-dibromo-[1,2,5]thiadiazolo[3,4-c]pyridine 2 by a combination of two reactions—aromatic nucleophilic substitution SNAr and Buchwald–Hartwig cross-coupling. The structure of the newly synthesized compounds was established by means of elemental analysis; high-resolution mass spectrometry; 1H, 13C NMR, IR and

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30

Cruz, Silvia, and Jaime Portilla. "Pyrazolopyridines and Pyrazolopyrimidines as Functional Dipolar Scaffolds: An Approach Regarding Synthesis and Photophysics." Chemistry 7, no. 4 (2025): 106. https://doi.org/10.3390/chemistry7040106.

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Pyrazolopyridines and pyrazolopyrimidines are 5:6 aza-fused N-heteroaromatic compounds (NHACs) comprising a pyrazole ring fused to a pyridine or pyrimidine ring. They exhibit dipolar behavior due to their π-excessive and π-deficient characteristics conferred by their five- and six-membered rings. These features favor their stability, reactivity, and structural diversity, offering numerous modular and functional derivatives (e.g., pyrazolo[1,2-a]pyridines, pyrazolo[1,5-a]pyrimidines, etc.). They have been utilized to obtain relevant chemicals in pharmaceuticals, photophysics, industry, and mate

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31

Arai, Tatsuo, and Takuya Kobayashi. "Hydrogen Bonding Induced Highly Selective Isomerization of an Olefin Having Heteroaromatic Rings." HETEROCYCLES 86, no. 2 (2012): 1129. http://dx.doi.org/10.3987/com-12-s(n)62.

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32

Leach, Andrew G., and Nathan J. Kidley. "Quantitatively Interpreted Enhanced Inhibition of Cytochrome P450s by Heteroaromatic Rings Containing Nitrogen." Journal of Chemical Information and Modeling 51, no. 5 (2011): 1048–63. http://dx.doi.org/10.1021/ci2000506.

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33

Sato, Masaru, Shinsuke Tanaka, Seiji Ebine, Kenichi Morinaga, and Sadatoshi Akabori. "Syntheses of ferrocenophanes containing aromatic or heteroaromatic rings in the bridging chain." Journal of Organometallic Chemistry 289, no. 1 (1985): 91–95. http://dx.doi.org/10.1016/0022-328x(85)88030-x.

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34

Nguyen, Ha Vinh Lam, Walther Caminati, and Jens-Uwe Grabow. "The LAM of the Rings: Large Amplitude Motions in Aromatic Molecules Studied by Microwave Spectroscopy." Molecules 27, no. 12 (2022): 3948. http://dx.doi.org/10.3390/molecules27123948.

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Large amplitude motions (LAMs) form a fundamental phenomenon that demands the development of specific theoretical and Hamiltonian models. In recent years, along with the strong progress in instrumental techniques on high-resolution microwave spectroscopy and computational capacity in quantum chemistry, studies on LAMs have become very diverse. Larger and more complex molecular systems have been taken under investigation, ranging from series of heteroaromatic molecules from five- and six-membered rings to polycyclic-aromatic-hydrocarbon derivatives. Such systems are ideally suited to create fam

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35

Sousa, Rui, Narayana Subbiah Hari Narayana Moorthy, Pedro Alexandrino Fernandes, Maria Joao Ramos, and Natércia Fernandes Brás. "Binding Mode Prediction and Identification of New Lead Compounds from Natural Products as 3-OST Enzyme Inhibitors." Letters in Drug Design & Discovery 17, no. 9 (2020): 1186–96. http://dx.doi.org/10.2174/1570180817666200313105944.

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Background and Introduction: The availability of antiviral medicines for the treatment of viral diseases is limited, hence the discovery of novel bioactive molecules is required. The present investigation has been carried out to develop novel 3-O-sulfotransferase enzyme inhibitors to treat viral diseases. Method: Virtual screening study (QSAR, docking and pharmacophore analysis) and binding mode analysis have been performed on a dataset collected from the literature (synthetic and natural compounds). Results: The docking studies showed that Glu184, His186, Lys215 and Lys368 residues establishe

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36

Reibnegger, Gilbert. "An ab initio and density functional theory study on neutral pterin radicals." Pteridines 26, no. 4 (2015): 135–42. http://dx.doi.org/10.1515/pterid-2015-0008.

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AbstractThe electronic structures of the five radicals resulting from homolytic elimination of one of the hydrogen atoms from the most stable tautomeric form of neutral pterin were investigated in gas phase as well as in aqueous solution. Molecular wave functions obtained by density functional theory were analysed by quantum theory of atoms in molecules and electron localisation functions (ELF). Spin densities of the radicals as well as electrostatic potential functions were analysed. Radicals resulting from elimination of N-bonded hydrogen atoms are more stable in comparison with radicals obt

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37

Guan, Jinming, Christina Spry, Erick T. Tjhin, et al. "Exploring Heteroaromatic Rings as a Replacement for the Labile Amide of Antiplasmodial Pantothenamides." Journal of Medicinal Chemistry 64, no. 8 (2021): 4478–97. http://dx.doi.org/10.1021/acs.jmedchem.0c01755.

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38

Šket, Boris, Marko Zupan, Nataša Zupančič, and Barbara Pahor. "Photosubstitution reactions on aromatic and heteroaromatic rings evidence for addition and substitution mechanism." Tetrahedron 47, no. 27 (1991): 5029–42. http://dx.doi.org/10.1016/s0040-4020(01)80966-2.

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39

ELNAGDI, M. H., M. R. H. ELMOGHAYER, and K. U. SADEK. "ChemInform Abstract: Chemistry of Pyrazoles Condensed to Heteroaromatic Five- and Six- Membered Rings." ChemInform 22, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199104357.

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40

Arun, Rajale Pratik, and Trupti Thange. "Design, Synthesis, and Biological Evaluation of Anti-prostate Cancer Agent." INTERANTIONAL JOURNAL OF SCIENTIFIC RESEARCH IN ENGINEERING AND MANAGEMENT 07, no. 10 (2023): 1–11. http://dx.doi.org/10.55041/ijsrem26291.

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In search of more effective chemotherapeutics for the treatment of castration-resistant prostate cancer. The 1,3- thiazolidine-2,4-diones possess a wide diversity of important biochemical effects and interesting pharmacological properties. 1,9-diarylnona-1,3,6,8-tetraen-5-ones bearing two identical terminal heteroaromatic rings have been successfully synthesized through Wittig reaction followed by Horner-Wadsworth-Emmons reaction. The cell proliferation assay was employed to assess their anti-proliferative effects toward both androgen-sensitive and androgen-insensitive human prostate cancer ce

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41

Cador, Aël, Samia Kahlal, Gary J. Richards, Jean-François Halet, and Jonathan P. Hill. "Protic Processes in an Extended Pyrazinacene: The Case of Dihydrotetradecaazaheptacene." Molecules 29, no. 10 (2024): 2407. http://dx.doi.org/10.3390/molecules29102407.

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Pyrazinacenes are linearly fused heteroaromatic rings, with N atoms replacing all apical CH moieties. Component rings may exist in a reduced state, having NH groups instead of N, causing cross-conjugation. These compounds have interesting optical and electronic properties, including strong fluorescence in the near-infrared region and photocatalytic properties, leading to diverse possible applications in bio-imaging and organic synthesis, as well as obvious molecular electronic uses. In this study, we investigated the behavior of seven-ring pyrazinacene 2,3,11,12-tetraphenyl-7,16-dihydro-1,4,5,

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42

Ohta, Akihiro, Tokuhiro Watanabe, and Masakatsu Ohta. "Introduction of the C-Substituted into the N-Heteroaromatic Rings Using Alkyl- and Arylmetals." HETEROCYCLES 24, no. 1 (1986): 265. http://dx.doi.org/10.3987/r-1986-01-0265.

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43

Chawdhury, N., A. Köhler, R. H. Friend, et al. "Synthesis and Electronic Structure of Platinum-Containing Poly-ynes with Aromatic and Heteroaromatic Rings." Macromolecules 31, no. 3 (1998): 722–27. http://dx.doi.org/10.1021/ma971267u.

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44

Li, Zhun, Yang Wen, Ying Wang, and Shaomin Zhu. "Highly transparent and organosoluble polyimides derived from 2,2′-bis[4-(5-amino-2-pyridinoxy) phenyl] propane." High Performance Polymers 29, no. 2 (2016): 161–69. http://dx.doi.org/10.1177/0954008316632291.

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Two new isomers containing pyridine ring diamine monomers, 2,2′-bis[4-(5-amino-2-pyridinoxy)phenyl] propane (1b) and 2,2′-bis[4-(6-amino-3-pyridinoxy)phenyl] propane (2b), were prepared via a simple nucleophilic reaction of 2-chloro-5-nitropyridine and 5-bromo-2-nitropyridine with bisphenol A in the presence of potassium carbonate, respectively. A series of polyimides (PIs) were obtained from the heterocyclic diamine with various commercially available aromatic dianhydrides via the conventional two-step method. These obtained PIs were investigated in aspects of their solubility, thermal, mecha

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45

Guchhait, Sankar Kumar, and Meenu Saini. "Chan–Lam N-arylation and C–H amination with heteroaromatic ring-NH: an approach to access extended-fused imidazo[1,2-a]-pyridines/pyrazines." New Journal of Chemistry 44, no. 2 (2020): 308–12. http://dx.doi.org/10.1039/c9nj04966e.

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46

Luh, Tien-Yau, Hsin-Chieh Lin, and Chih-Ming Chou. "Heterophenes revisited." Pure and Applied Chemistry 80, no. 3 (2008): 475–84. http://dx.doi.org/10.1351/pac200880030475.

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By employing the furan annulation protocol, a new series of furan-containing teraryl [n.2]cyclophenes (n = 2-6 and 12) are prepared. These cyclophenes exhibit charge-transfer character in the absorption spectra and unusually large Stokes shifts in the emission spectra. They have neither particularly strong electron-donating moieties nor electron-withdrawing groups, but exhibit unusual second-order nonlinear optical (NLO) properties. The π-systems in teraryl system and in the bridging double bond are highly twisted. Interaction between these twisted π-systems may account for the significant enh

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47

Megala, M., and Beulah J. M. Rajkumar. "Heteroaromatic rings as linkers for quercetin-based dye-sensitized solar cell applications: a TDDFT investigation." Journal of Computational Electronics 18, no. 4 (2019): 1128–38. http://dx.doi.org/10.1007/s10825-019-01398-0.

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48

Pozzo, Jean-Luc, Vladimir Lokshin, André Samat, Robert Guglielmetti, Roger Dubest, and Jean Aubard. "Effect of heteroaromatic annulation with five-membered rings on the photochromism of 2H- [1] -benzopyrans." Journal of Photochemistry and Photobiology A: Chemistry 114, no. 3 (1998): 185–91. http://dx.doi.org/10.1016/s1010-6030(98)00215-9.

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Chin, Chong Shik, Yongsun Park, and Byeongno Lee. "Regioselective catalytic hydrogenation of nitrogen rings of fused heteroaromatic compounds with an iridium-triphenylphosphine complex." Catalysis Letters 31, no. 2-3 (1995): 239–43. http://dx.doi.org/10.1007/bf00808836.

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SKET, B., M. ZUPAN, N. ZUPANCIC, and B. PAHOR. "ChemInform Abstract: Photosubstitution Reactions on Aromatic and Heteroaromatic Rings. Evidence for Addition and Substitution Mechanism." ChemInform 22, no. 41 (2010): no. http://dx.doi.org/10.1002/chin.199141071.

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