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Journal articles on the topic 'Pechmann dyes'

Author: Grafiati
Published: 10 March 2023

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1

Hopf, Henning, Peter G. Jones, Alina Nicolescu, Elena Bicu, Lucian M. Birsa, and Dalila Belei. "A Facile Synthesis of Pechmann Dyes." Chemistry - A European Journal 20, no. 19 (April 2, 2014): 5565–68. http://dx.doi.org/10.1002/chem.201400329.

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2

Wang, Xiao-Ye, Meng-Wen Zhang, Fang-Dong Zhuang, Jie-Yu Wang, and Jian Pei. "Lactone-fused electron-deficient building blocks for n-type polymer field-effect transistors: synthesis, properties, and impact of alkyl substitution positions." Polymer Chemistry 7, no. 12 (2016): 2264–71. http://dx.doi.org/10.1039/c6py00143b.

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Dilactone-based Pechmann dyes were incorporated into conjugated polymers for n-type field-effect transistors, providing a new design concept of electron-deficient building blocks for polymer semiconductors.
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3

Calamante, Massimo, Gianna Reginato, Alessio Dessì, Matteo Bartolini, Lorenzo Zani, and Alessandro Mordini. "Extending the Conjugation of Pechmann Lactone Thienyl Derivatives: A New Class of Small Molecules for Organic Electronics Application." Synthesis 50, no. 06 (December 20, 2017): 1284–92. http://dx.doi.org/10.1055/s-0036-1591856.

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The preparation and spectroscopic characterization of some symmetrical small molecules containing the disubstituted (E)-3,3′-bifuranylidene-2,2′-dione chromophore (the so-called Pechmann lactone) and featuring an extended conjugation are reported. The synthetic approach of such compounds is based on the Stille–Migita coupling reaction, which is carried out in very mild conditions, suitable to be applied with the very sensitive Pechmann core. The absorption and emission spectra of the new molecules obtained have been recorded in solution and clearly show how their photophysical properties can be modulated by a proper choice of the (hetero)aromatic terminal groups. The compounds prepared in this study (or close analogues thereof) have interesting optical properties and could find application as semiconductors in organic electronics or as near-IR fluorescent dyes.
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4

Aysha, Tarek, Mervat El-Sedik, Hamada M. Mashaly, Morsy A. El-Apasery, Oldřich Machalický, and Radim Hrdina. "Synthesis, characterisation, and applications of isoindigo/Pechmann dye heteroanalogue hybrid dyes on polyester fabric." Coloration Technology 131, no. 4 (July 8, 2015): 333–41. http://dx.doi.org/10.1111/cote.12161.

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5

Dessì, Alessio, Adalgisa Sinicropi, Sanaz Mohammadpourasl, Riccardo Basosi, Maurizio Taddei, Fabrizia Fabrizi de Biani, Massimo Calamante, et al. "New Blue Donor–Acceptor Pechmann Dyes: Synthesis, Spectroscopic, Electrochemical, and Computational Studies." ACS Omega 4, no. 4 (April 26, 2019): 7614–27. http://dx.doi.org/10.1021/acsomega.8b03560.

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6

Kantchev, Eric Assen B., Tyler B. Norsten, Marilyn L. Y. Tan, Joey J. Y. Ng, and Michael B. Sullivan. "Thiophene-Containing Pechmann Dyes and Related Compounds: Synthesis, and Experimental and DFT Characterisation." Chemistry - A European Journal 18, no. 2 (December 8, 2011): 695–708. http://dx.doi.org/10.1002/chem.201101903.

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7

Wazzan, Nuha, and Ahmad Irfan. "Exploring the optoelectronic and charge transport properties of Pechmann dyes as efficient OLED materials." Optik 197 (November 2019): 163200. http://dx.doi.org/10.1016/j.ijleo.2019.163200.

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8

Kantchev, Eric Assen B., Tyler B. Norsten, and Michael B. Sullivan. "Time-dependent density functional theory (TDDFT) modelling of Pechmann dyes: from accurate absorption maximum prediction to virtual dye screening." Organic & Biomolecular Chemistry 10, no. 33 (2012): 6682. http://dx.doi.org/10.1039/c2ob25806d.

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9

Wazzan, Nuha. "The nonlinear optical properties of acyclic triarylamine-conjugated dimethyl diethynylfumarate and its two cyclic Pechmann dyes derivatives: A theoretical study." Optik 207 (April 2020): 163895. http://dx.doi.org/10.1016/j.ijleo.2019.163895.

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10

Kantchev, Eric Assen B., Tyler B. Norsten, and Michael B. Sullivan. "Chemically accurate and computationally-efficient time-dependent density functional theory (TDDFT) modeling of the UV/Vis spectra of Pechmann dyes and related compounds." Procedia Computer Science 4 (2011): 1157–66. http://dx.doi.org/10.1016/j.procs.2011.04.124.

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11

Hayashi, Mikihiro, Fumiyuki Toshimitsu, Ryota Sakamoto, and Hiroshi Nishihara. "Double Lactonization in Triarylamine-Conjugated Dimethyl Diethynylfumarate: Formation of Intensely Colored and Luminescent Quadrupolar Molecules Including a Missing Structural Isomer of Pechmann Dyes." Journal of the American Chemical Society 133, no. 37 (September 21, 2011): 14518–21. http://dx.doi.org/10.1021/ja2054176.

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12

Qi, Penglin, Zhijie Wang, Zitong Liu, Sifen Yang, Yang Yang, Jingjing Yao, Guanxin Zhang, and Deqing Zhang. "Conjugated donor–acceptor terpolymers entailing the Pechmann dye and dithienyl-diketopyrrolopyrrole as co-electron acceptors: tuning HOMO/LUMO energies and photovoltaic performances." Polymer Chemistry 7, no. 23 (2016): 3838–47. http://dx.doi.org/10.1039/c6py00400h.

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13

Norsten, Tyler B., Eric Assen B. Kantchev, and Michael B. Sullivan. "Thiophene-Containing Pechmann Dye Derivatives." Organic Letters 12, no. 21 (November 5, 2010): 4816–19. http://dx.doi.org/10.1021/ol1019772.

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14

Thilanga Liyanage, A. D., Begoña Milián-Medina, Bei Zhang, Johannes Gierschner, and Mark D. Watson. "¿Conjugated? Copolymers from a Pechmann Dye Derivative." Macromolecular Chemistry and Physics 217, no. 18 (July 22, 2016): 2068–73. http://dx.doi.org/10.1002/macp.201600175.

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15

Aysha, Tarek, Stanislav Luňák, Antonín Lyčka, Jan Vyňuchal, Zdeněk Eliáš, Aleš Růžička, Zdeňka Padělková, and Radim Hrdina. "Synthesis, structure, absorption and fluorescence of Pechmann dye heteroanalogues." Dyes and Pigments 98, no. 3 (September 2013): 530–39. http://dx.doi.org/10.1016/j.dyepig.2013.04.010.

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16

Luo, Hewei, Xiaobiao Dong, Zhengxu Cai, Lizhen Wang, and Zitong Liu. "Pechmann Dye-Based Molecules Containing Fluorobenzene Moieties for Ambipolar Organic Semiconductors." Asian Journal of Organic Chemistry 7, no. 3 (February 28, 2018): 592–97. http://dx.doi.org/10.1002/ajoc.201700669.

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17

Efrem, Amsalu, Marc Courté, Kai Wang, Denis Fichou, and Mingfeng Wang. "Synthesis and characterization of γ-lactone-Pechmann dye based donor-acceptor conjugated polymers." Dyes and Pigments 134 (November 2016): 171–77. http://dx.doi.org/10.1016/j.dyepig.2016.07.013.

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18

Chithanna, Sivanna, and Ding-Yah Yang. "Construction of 2-pyridones via oxidative cyclization of enamides: access to Pechmann dye derivatives." Organic & Biomolecular Chemistry 19, no. 7 (2021): 1565–74. http://dx.doi.org/10.1039/d0ob02376k.

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19

Cai, Zhengxu, Zitong Liu, Hewei Luo, Penglin Qi, Guanxin Zhang, and Deqing Zhang. "π-Extented Conjugated Polymers Entailing Pechmann Dye Moieties for Solution-Processed Ambipolar Organic Semiconductors." Chinese Journal of Chemistry 32, no. 8 (August 2014): 788–96. http://dx.doi.org/10.1002/cjoc.201400423.

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20

Fukazawa, Aiko, Makoto Adachi, Ken Nakakura, Shohei Saito, and Shigehiro Yamaguchi. "S-Pechmann dye: a thiolactone-containing organic dye with a pronounced electron-accepting character and its solid-state photophysical properties." Chemical Communications 49, no. 64 (2013): 7117. http://dx.doi.org/10.1039/c3cc41007b.

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21

Fukazawa, Aiko, Makoto Adachi, Ken Nakakura, Shohei Saito, and Shigehiro Yamaguchi. "ChemInform Abstract: S-Pechmann Dye: A Thiolactone-Containing Organic Dye with a Pronounced Electron-Accepting Character and Its Solid-State Photophysical Properties." ChemInform 44, no. 50 (November 21, 2013): no. http://dx.doi.org/10.1002/chin.201350205.

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22

Bhattacharya, Labanya, Gautomi Gogoi, Sagar Sharma, Alex Brown, and Sridhar Sahu. "Promising small molecule Pechmann dye analogue donors with low interfacial charge recombination for photovoltaic application: A DFT study." Materials Today Communications 28 (September 2021): 102555. http://dx.doi.org/10.1016/j.mtcomm.2021.102555.

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23

Hodgson, Gregory K., Stefania Impellizzeri, and Juan C. Scaiano. "Dye synthesis in the Pechmann reaction: catalytic behaviour of samarium oxide nanoparticles studied using single molecule fluorescence microscopy." Chemical Science 7, no. 2 (2016): 1314–21. http://dx.doi.org/10.1039/c5sc03214h.

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24

Silver, Jack, Mustafa T. Ahmet, Keith Bowden, John R. Miller, Shahdah Rahmat, Christopher A. Reynolds, Alan Bashall, Mary McPartlin, and Jill Trotter. "Electrochromic behaviour and X-ray structure analysis of a Pechmann dye, (E)-5,5′-diphenyl-3,3′-bifuranylidene-2,2′-dione." J. Mater. Chem. 4, no. 8 (1994): 1201–4. http://dx.doi.org/10.1039/jm9940401201.

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25

Yang, Si-Fen, Zi-Tong Liu, Zheng-Xu Cai, He-Wei Luo, Peng-Lin Qi, Guan-Xin Zhang, and De-Qing Zhang. "Conjugated Donor–Acceptor Polymers Entailing Pechmann Dye-Derived Acceptor with Siloxane-Terminated Side Chains Exhibiting Balanced Ambipolar Semiconducting Behavior." Macromolecules 49, no. 16 (August 12, 2016): 5857–65. http://dx.doi.org/10.1021/acs.macromol.6b01440.

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26

Cai, Zhengxu, Yunlong Guo, Sifen Yang, Qian Peng, Hewei Luo, Zitong Liu, Guanxin Zhang, Yunqi Liu, and Deqing Zhang. "New Donor–Acceptor–Donor Molecules with Pechmann Dye as the Core Moiety for Solution-Processed Good-Performance Organic Field-Effect Transistors." Chemistry of Materials 25, no. 3 (January 14, 2013): 471–78. http://dx.doi.org/10.1021/cm303793g.

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27

Irikawa, Hajime, Norihide Adachi, and Hirokazu Muraoka. "Preparation and Absorption Spectral Properties of the Nitrogen Analogs of a Pechmann Dye and Its Isomeric Pyrano[4,3-c]pyran-1,5-dione." HETEROCYCLES 48, no. 7 (1998): 1415. http://dx.doi.org/10.3987/com-98-8176.

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28

Cai, Zhengxu, Hewei Luo, Penglin Qi, Jianguo Wang, Guanxin Zhang, Zitong Liu, and Deqing Zhang. "Alternating Conjugated Electron Donor–Acceptor Polymers Entailing Pechmann Dye Framework as the Electron Acceptor Moieties for High Performance Organic Semiconductors with Tunable Characteristics." Macromolecules 47, no. 9 (April 14, 2014): 2899–906. http://dx.doi.org/10.1021/ma5003694.

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29

Chaudhary, Diksha, Pooja Bedi, Soumava Santra, and Tanay Pramanik. "Synthesis and Biological Properties of Coumarin Analogue: A Brief Review." Letters in Organic Chemistry 18 (February 2, 2021). http://dx.doi.org/10.2174/1570178618666210202152452.

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: One of the most prominent aromatic organic chemical compound is Coumarin having formula C9H6O2 which is widely known for its benefits in drug industry. Colourless crystalline solid having sweet scent is coumarin’s physical identity. It serves various purposes such as in synthesis of medicines, laser dyes, perfumes and many more. Having enormous usages it becomes important to synthesize such compound so various reactions were performed in order to obtain coumarins. This review explicates the preparation of coumarin by Pechmann Condensation and its biological characteristics.
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