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1

HANSONGNERN, Kanidtha, Uraiwan CHANGSALUK, and Chaveng PAKAWATCHAI. "Crystal Structure of 5-Methyl-2-(phenylazo)pyridine." Analytical Sciences: X-ray Structure Analysis Online 24 (2008): x99—x100. http://dx.doi.org/10.2116/analscix.24.x99.

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2

Barf, Gert A., and Roger A. Sheldon. "Ruthenium(II) 2-(phenylazo)pyridine complexes as epoxidation catalysts." Journal of Molecular Catalysis A: Chemical 98, no. 3 (1995): 143–46. http://dx.doi.org/10.1016/1381-1169(95)00026-7.

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3

Hafijur, Rahaman, Bose Doyel, Banerjee Jaya, Kumar Ghosh Alak, and Kumar Ghosh Barindra. "Isolation of one-electron reduced product of [OsL3)2+ [L = 2-(arylazo)pyridines)." Journal of Indian Chemical Society Vol. 79, Sep 2002 (2002): 755–58. https://doi.org/10.5281/zenodo.5844300.

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Department of Chemistry, The University of Burdwan, Burdwan-713 104, India Department of Chemistry, Regional Engineering College, Durgapur-713 209, India <em>Manuscript received 10 August 2001, accepted 25 April 2002</em> The preparation of [OsL<sub>3</sub>]ClO<sub>4</sub>.H<sub>2</sub>O [L = 2-(phenylazo)pyridine (L<sup>1</sup>), 2-(<em>m</em>-tolylazo)pyridine (L<sup>2</sup>) and 2-(<em>p</em>-tolylazo)pyridine (L<sup>3</sup>)] via chemical/electrochemical reduction of [OsL<sub>3</sub>](ClO<sub>4</sub>)<sub>2</sub>.H<sub>2</sub>O is described. The paramagnetic compounds display a highly inte
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4

Ragon, Florence, Korcan Yaksi, Natasha F. Sciortino, et al. "Thermal Spin Crossover Behaviour of Two-Dimensional Hofmann-Type Coordination Polymers Incorporating Photoactive Ligands." Australian Journal of Chemistry 67, no. 11 (2014): 1563. http://dx.doi.org/10.1071/ch14188.

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Two spin crossover (SCO)-active 2D Hofmann-type framework materials, [Fe(3-PAP)2Pd(CN)4] (A) and [Fe(4-PAP)2Pd(CN)4] (B) containing the photoactive azo-benzene-type ligands 3-phenylazo-pyridine (3-PAP) and 4-phenylazo-pyridine (4-PAP) were prepared. These materials form non-porous Hofmann-type structures whereby 2D [FeIIPd(CN)4] grids are separated by 3- or 4-PAP ligands. The iron(ii) sites of both materials (A and B) undergo abrupt and hysteretic spin transitions with characteristic transition temperatures T1/2↓,↑: 178, 190 K (ΔT: 12 K) and T1/2↓,↑: 233, 250 K (ΔT: 17 K), respectively. Photo-
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5

Dougan, Sarah J., Michael Melchart, Abraha Habtemariam, Simon Parsons, and Peter J. Sadler. "Phenylazo-pyridine and Phenylazo-pyrazole Chlorido Ruthenium(II) Arene Complexes: Arene Loss, Aquation, and Cancer Cell Cytotoxicity." Inorganic Chemistry 45, no. 26 (2006): 10882–94. http://dx.doi.org/10.1021/ic061460h.

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6

Dougan, Sarah J., Michael Melchart, Abraha Habtemariam, Simon Parsons, and Peter J. Sadler. "Phenylazo-pyridine and Phenylazo-pyrazole chlorido Ruthenium(II) Arene Complexes: Arene Loss, Aquation, and Cancer Cell Cytotoxicity." Inorganic Chemistry 46, no. 4 (2007): 1508. http://dx.doi.org/10.1021/ic070028c.

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7

Lahiri, Goutam Kumar, Samaresh Bhattacharya, Sreebrata Goswami, and Animesh Chakravorty. "High-potential isomeric ruthenium(III) complexes of 2-(phenylazo)pyridine." Journal of the Chemical Society, Dalton Transactions, no. 2 (1990): 561. http://dx.doi.org/10.1039/dt9900000561.

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8

Kumar, Birendra, Rekha Rani, Dayanand Prasad, Praveen Kumar Singh, Amit Kumar, and Shivadhar Sharma. "Electronic Structure and Spectral Study of Some Five Coordinate Complexes of Copper (II)." Oriental Journal Of Chemistry 35, no. 4 (2019): 1463–68. http://dx.doi.org/10.13005/ojc/350430.

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1-phenylazo-2-nephthol has been synthesized and used for complexation with Cu(II) metal ion along with pyridine, α-picoline, β- picoline, γ-picoline and water as secondary ligands. On the basis of elemental analysis and molar conductivity complexes were formulated as CuL2X [Where L is the prime ligand i.e 1-phenyl-azo-2-nephthol and X is the secondary ligand i.e. pyridine, α-picoline, β-picoline, and H2O.] The magnetic moment of these complexes (1.80 - 1.83 BM) indicates that these complexes are magnetically dilute. The appearance of 3 bands in the electronic spectra of complexes rules out the
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9

Hansongnern, Kanidtha, Supojjanee Sansook, Thassani Romin, Arunpatcha Nimthong Roldan та Chaveng Pakawatchai. "Crystal structure of [3-amino-2-(phenyldiazenyl)pyridine]chlorido(η6-p-cymene)ruthenium(II) chloride". Acta Crystallographica Section E Crystallographic Communications 71, № 10 (2015): m185—m186. http://dx.doi.org/10.1107/s2056989015017466.

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The title compound, [RuCl(C10H14)(C11H10N4)]Cl is an RuIIcomplex in which an η6-p-cymene ligand, two N atoms of 3-amino-2-(phenylazo)pyridine and one Cl ion form a piano-stool coordination environment around the metal ion. In the crystal structure, N—H...Cl hydrogen bonds play an important role in the formation of the supramolecular zigzag chain along thea-axis direction. Disorder is observed for the isopropyl group with site-occupancy factors refined to 0.78 (5) and 0.22 (5).
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10

Ackermann, Martin N., Jerome W. Naylor, Eric J. Smith, et al. "Iron carbonyl complexes of 2-(phenylazo)pyridines. First example of a six-electron, bridging 2-(phenylazo)pyridine ligand." Organometallics 11, no. 5 (1992): 1919–26. http://dx.doi.org/10.1021/om00041a026.

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11

PANNEERSELVAM, Kaliyamoorthy, Kanidtha HANSONGNERN, Nattaporn RATTANAWIT, Fen-Ling LIAO, and Tian-Huey LU. "Crystal Structure of the [Protonated 2-(phenylazo)pyridine and Protonated 2-(4-hydroxyphenylazo)-pyridine (3:1)]tetrafluoroborate." Analytical Sciences 16, no. 10 (2000): 1107–8. http://dx.doi.org/10.2116/analsci.16.1107.

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12

HANSONGNERN, Kanidtha, Uraiwan CHANGSALUK, and Chaveng PAKAWATCHAI. "Crystal Structure of ccc-Bis(5-methyl-2-(phenylazo)pyridine)-dichlororuthenium(II)." Analytical Sciences: X-ray Structure Analysis Online 24 (2008): x171—x172. http://dx.doi.org/10.2116/analscix.24.x171.

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13

HANSONGNERN, Kanidtha, Luksamee SAHAVISIT, and Chaveng PAKAWATCHAI. "Crystal Structure of cis-Bis(5-chloro-2-(phenylazo)pyridine)-dichlororuthenium(II)." Analytical Sciences: X-ray Structure Analysis Online 24 (2008): x57—x58. http://dx.doi.org/10.2116/analscix.24.x57.

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14

Das, Anindya, Shie-Ming Peng, and Samaresh Bhattacharya. "Chemistry of 2-(phenylazo)pyridine complexes of osmium: synthesis, characterization and reactivities." Polyhedron 19, no. 10 (2000): 1227–32. http://dx.doi.org/10.1016/s0277-5387(00)00378-8.

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15

Tongying, Pornthip, Suthirat Yoopensuk, Nararak Leesakul, and Yuthana Tantirungrotechai. "Exploring photochemistry of 2-(phenylazo)pyridine dye by using TDDFT/DFT methods." Canadian Journal of Chemical Engineering 90, no. 4 (2011): 860–64. http://dx.doi.org/10.1002/cjce.20678.

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16

ACKERMANN, M. N., J. W. NAYLOR, E. J. SMITH, et al. "ChemInform Abstract: Iron Carbonyl Complexes of 2-(Phenylazo)pyridines. The First Example of a Six-Electron, Bridging 2-(Phenylazo)pyridine Ligand." ChemInform 23, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199236236.

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17

HANSONGNERN, Kanidtha, Uraiwan SAETEAW, Golam MOSTAFA, Fen-Ling LIAO, and Tian-Huey LU. "Crystal Structure of Bromo(2,2': 6',2"-terpyridine)(2-(phenylazo)-pyridine)ruthenium(II) Tetrafluoroborate." Analytical Sciences 19, no. 6 (2003): 971–72. http://dx.doi.org/10.2116/analsci.19.971.

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18

Partha, Majumdar. "Synthesis, spectral characterization and redox properties of a hetero-tetranuclear biimidazolato-bridged complex with OsII 2AgI 2 core." Journal of Indian Chemical Society Vol. 93, Jan 2016 (2016): 19–23. https://doi.org/10.5281/zenodo.5607031.

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Department of Chemistry, Krishnanath College, Berhampore-742 101, West Bengal, India <em>E-mail</em> : kncpm@rediffmail.com <em>Manuscript received online 12 June 2015, accepted 20 August 2015</em> A hetero-tetranuclear complex of osmium(II) and silver(I) containing the terminal ligand 2-(phenylazo)pyridine(pap) and the bridging ligand 2,2&acute;-biimidazolate (biim<sup>2&ndash;</sup>) has been synthesized. The complex is characterized by the analysisof physicochemical data. Electron spray ionization mass spectrum (ESIMS) of the complex has been reported whichauthenticates its formulation. The
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19

Ackermann, Martin N., Suzanne R. Kiihne, Patricia A. Saunders, et al. "Synthesis and studies of cis-Mo(CO)2(L–L′)2 and Mo(L–L′)3 complexes of 2-(phenylazo)pyridines (L–L′) and the crystal structures of Mo(CO)2(4-methyl-2-(phenylazo)pyridine)2 and Mo(4-methyl-2-(phenylazo)pyridine)3." Inorganica Chimica Acta 334 (May 2002): 193–203. http://dx.doi.org/10.1016/s0020-1693(02)00851-4.

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20

Doyel, Bose, Rahaman Hafijur, Banerjee Jaya, Kumar Mallick Tapan, Sinha Chittaranjan, and Kumar Ghosh Barindra. "Mixed ligand complexes of osmium(II/III/IV)-2,2' -dipyridylamine synthesis and redox behavior." Journal of Indian Chemical Society Vol. 79, Sep 2002 (2002): 713–18. https://doi.org/10.5281/zenodo.5843897.

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Department of Chemistry, The University of Burdwan, Burdwan-713 104, India <em>E-mail :</em> barin_1 @yahoo.co.uk&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;<em>Fax : </em>91-342-530452 <em>Manuscript received 27 August 2001, revised 11 February 2002, accepted 25 April 2002</em> Eight mixed ligand compounds of osmium(II), -(III), -(IV) of general formula, [Os(dpya)L<sub>2</sub>]<sup>z+</sup> [dpya = 2,2&#39;-dipyridylamine; L = 2-(phenylazo)pyridine (L<sup>1</sup>), 2-(<em>m</em>-tolylazo)pyridine (L<sup>2</sup>), 2,2&#39;-bipyridyl (L<sup>3</sup>),
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21

Ahmed, Hoda, Mohamed Hagar, and Omaima Alhaddad. "Phase Behavior and DFT Calculations of Laterally Methyl Supramolecular Hydrogen-Bonding Complexes." Crystals 9, no. 3 (2019): 133. http://dx.doi.org/10.3390/cryst9030133.

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Four new series of laterally methyl-substituted hydrogen-bonded supramolecular complexes were prepared. The prepared complexes were thermally investigated by differential scanning calorimetry (DSC) and phases identified by polarized light microscopy (PLM). Supramolecular hydrogen-bonded complexes formed from a 1:1 mixture of any two derivatives, bearing different alkoxy chains, of 4-alkoxyphenylazobenzoic acid and 4-(2-(pyridin-4-yl)diazenyl-(2-(or 3-)methylphenyl) 4-alkoxybenzoate. The investigated 1:1 mixture made by introducing a lateral methyl group by different spatial orientation angles
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22

Ratanaphan, Adisorn, Tidarat Nhukeaw, Pornvichai Temboot, and Kanidtha Hansongnern. "DNA-binding properties of ruthenium(II) complexes with the bidentate ligand 5-chloro-2-(phenylazo)pyridine." Transition Metal Chemistry 37, no. 2 (2012): 207–14. http://dx.doi.org/10.1007/s11243-012-9576-5.

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23

Agarkar, Harshawardhan, and Dipanwita Das. "The photo-switching study of guest 2-(phenylazo)pyridine (PAP) embedded in solid host material MOF-5." Journal of Molecular Structure 1184 (May 2019): 435–42. http://dx.doi.org/10.1016/j.molstruc.2019.02.059.

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24

HANSONGNERN, Kanidtha, Uraiwan CHANGSALUK, Jian-Sung WU, and Tian-Huey LU. "Crystal Structure of the [Ru(azpy)2(bpy)](PF6)2 Complex (azpy = 2-(phenylazo)pyridine, bpy = 2,2′-bipyridine)." Analytical Sciences: X-ray Structure Analysis Online 23 (2007): x131—x132. http://dx.doi.org/10.2116/analscix.23.x131.

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25

Deb, Alok Kumar, and Sreebrata Goswami. "Reactions of primary aromatic amines with strongly electrophilic no coordinated to a ruthenium complex of 2-(phenylazo)pyridine." Polyhedron 10, no. 15 (1991): 1799–801. http://dx.doi.org/10.1016/s0277-5387(00)83802-4.

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26

Bugaeva, Aleksandra I., and Yuriy G. Slizhov. "SILICA GEL MODIFICATION BY NICKEL(II) COMPLEXES WITH NITROGEN- AND OXYGEN-CONTAINING ORGANIC LIGANDS FOR GAS CHROMATOGRAPHY." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 64, no. 1 (2020): 59–66. http://dx.doi.org/10.6060/ivkkt.20216401.6299.

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Gas chromatographic sorbents based on Siloсhrome S-80 adsorptively modified with 8-hydroxyquinolinate, 1-phenylazo-2-naphtholate and 2-nitroso-1-naphtholate of nickel(II) have been obtained. It has been established that the thermal stability (up to 170–350 °C) of chelate-containing sorbents is sufficient for carrying out gas chromatographic separations. The IR and Raman spectra of the obtained materials confirmed the success of the complexation processes in the synthesis of complex nickel(II) compounds and the retention of coordination bonds after the deposition of chelates on silica gel. The
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27

Bugaeva, Aleksandra I., and Yuriy G. Slizhov. "SILICA GEL MODIFICATION BY NICKEL(II) COMPLEXES WITH NITROGEN- AND OXYGEN-CONTAINING ORGANIC LIGANDS FOR GAS CHROMATOGRAPHY." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 64, no. 1 (2020): 59–66. http://dx.doi.org/10.6060/ivkkt.20216401.6299.

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Gas chromatographic sorbents based on Siloсhrome S-80 adsorptively modified with 8-hydroxyquinolinate, 1-phenylazo-2-naphtholate and 2-nitroso-1-naphtholate of nickel(II) have been obtained. It has been established that the thermal stability (up to 170–350 °C) of chelate-containing sorbents is sufficient for carrying out gas chromatographic separations. The IR and Raman spectra of the obtained materials confirmed the success of the complexation processes in the synthesis of complex nickel(II) compounds and the retention of coordination bonds after the deposition of chelates on silica gel. The
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28

Klenina, O. V., T. I. Chaban, V. V. Ogurtsov, I. G. Chaban, and I. Ya Golos. "3D Pharmacophore modeling in the molecules of 5,7-dimethyl-6-phenylazo-3H-thiazolo[4,5-b]pyridine-2-one derivatives." Journal of Organic and Pharmaceutical Chemistry 12, no. 1(45) (2014): 60–68. http://dx.doi.org/10.24959/ophcj.14.768.

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29

Vittaya, Luksamee, Nararak Leesakul, Saowanit Saithong, et al. "Synthesis, characterization, and biological studies of novel Ni(II) and Zn(II) complexes with 5-chloro-2-(phenylazo)pyridine." ScienceAsia 43, no. 3 (2017): 175. http://dx.doi.org/10.2306/scienceasia1513-1874.2017.43.175.

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30

Michalski, J., E. Kucharska, M. Wandas, et al. "Crystal structure, vibrational and NMR studies and chemical quantum calculations of 2-phenylazo-5-nitro-6-methyl-pyridine (C12H10N4O2)." Journal of Molecular Structure 744-747 (June 2005): 377–92. http://dx.doi.org/10.1016/j.molstruc.2004.11.072.

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31

Tan, Xing-wu, Xiao-hua Xie, Jin-ye Chen, and Shu-zhong Zhan. "Synthesis, structures and properties of cobalt(II) and copper(I) complexes of 2,6-diamino-3-[(2-carboxymethyl)phenylazo]-pyridine." Inorganic Chemistry Communications 13, no. 12 (2010): 1455–58. http://dx.doi.org/10.1016/j.inoche.2010.08.015.

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32

Ackermann, Martin N., William G. Fairbrother, Neelim S. Amin, Charles J. Deodene, Carl M. Lamborg, and Paul T. Martin. "Tetracarbonylmolybdenum complexes of 2-(phenylazo)pyridine ligands. Correlations of molybdenum-95 chemical shifts with electronic, infrared, and electrochemical properties." Journal of Organometallic Chemistry 523, no. 2 (1996): 145–51. http://dx.doi.org/10.1016/0022-328x(96)06346-2.

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33

Guo, Yanmei, Yunhui Hao, Lei Gao, and Hongxun Hao. "Photomechanical Molecular Crystals of an Azopyridine Derivative and Its Zinc(II) Complex: Synthesis, Crystallization and Photoinduced Motion." Crystals 10, no. 2 (2020): 92. http://dx.doi.org/10.3390/cryst10020092.

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In this work, photomechanical molecular crystals of 4-(4-(6-Hydroxyhexyloxy) phenylazo) pyridine (6cazpy) and its zinc(II) organic complex (complex-I) were synthesized and crystallized. DSC and TGA were used to characterize and compare properties of 6cazpy and its complex-I crystals. Photoinduced motions of 6cazpy crystals and its complex-I crystals were investigated and compared by UV/Vis irradiation. Bending away motions from the light source were observed from both 6cazpy crystals and its complex-I crystals. The bending away motion was attributed to the trans-to-cis photoisomerization of az
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34

Rekha, Rani, Ranjan Rajeeva, C. Bhattacharjee N., Sharma S., and Suraiya Afshan. "Spectroscopic characterization of some copper(II) complexes." Journal of Indian Chemical Society Vol. 90, Mar 2013 (2013): 331–36. https://doi.org/10.5281/zenodo.5769591.

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University Department of Chemistry, Magadh University, Bodh Gaya-824 234, Bihar, India G.B.M. College, Gaya-823 001, Bihar, India <em>Manuscript received 29 November 2011, revised 02 May 2012, accepted 14 May 2012</em> 1-(Phenylazo)-2-naphthol (PANH) has three potential donor sites and thus it acts as a very good chelating agent. This ligand has been used for complexation with Cu<sup>II</sup>&nbsp;ions to synthesize the complexes of general formula Cu(PAN)<sub>2</sub> Ln, where L = secondary ligands like pyridine, picoline, H<sub>2</sub>O&nbsp;and n = 0, 1&nbsp;and 2. These complexes have been
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35

Krause, Kirsten, R. A. Krause, Sine Larsen, Bjarne Rasmussen, and Eberhard Hoyer. "Complexes of 2-(Phenylazo)pyridine. Chemical Reactivity and Crystal and Molecular Structure of Conformers of [Ru(azpy)2(N3)2]." Acta Chemica Scandinavica 39a (1985): 375–88. http://dx.doi.org/10.3891/acta.chem.scand.39a-0375.

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36

Kamar, Kunal K., Amrita Saha, Alfonso Castiñeiras, Chen-Hsiung Hung, and Sreebrata Goswami. "Chromium Complexes of an IsomericN-Donor Ligand, 2-[(N-Arylamino)phenylazo]pyridine: Amination Reactions, X-ray Structure, and Redox Properties." Inorganic Chemistry 41, no. 17 (2002): 4531–38. http://dx.doi.org/10.1021/ic0201497.

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37

Melánová, Klára, Petr Kovář, Martina Gamba, et al. "Structural Arrangement of 4-[4-(Dimethylamino)phenylazo]pyridine Push-Pull Molecules in Acidic Layered Hosts Solved by Experimental and Calculation Methods." European Journal of Inorganic Chemistry 2017, no. 1 (2016): 115–23. http://dx.doi.org/10.1002/ejic.201601053.

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38

Das, Chayan, Amrita Saha, Chen-Hsiung Hung, Gene-Hsiang Lee, Shie-Ming Peng, and Sreebrata Goswami. "Ruthenium Complexes of 2-[(4-(Arylamino)phenyl)azo]pyridine Formed via Regioselective Phenyl Ring Amination of Coordinated 2-(Phenylazo)pyridine: Isolation of Products, X-ray Structure, and Redox and Optical Properties." Inorganic Chemistry 42, no. 1 (2003): 198–204. http://dx.doi.org/10.1021/ic0203724.

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39

Majumdar, Partha, Shie-Ming Peng, and Sreebrata Goswami. "Biimidazole complexes of ML22+ [M = Ru or Os, L = 2-(phenylazo)pyridine]. Synthesis, structure and redox properties of mono- and di-nuclear complexes ‡." Journal of the Chemical Society, Dalton Transactions, no. 10 (1998): 1569–74. http://dx.doi.org/10.1039/a801071d.

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40

Hotze, Anna C. G., Aldrik H. Velders, Franco Ugozzoli та ін. "Synthesis, Characterization, and Crystal Structure of α-[Ru(azpy)2(NO3)2] (azpy = 2-(Phenylazo)pyridine) and the Products of Its Reactions with Guanine Derivatives". Inorganic Chemistry 39, № 17 (2000): 3838–44. http://dx.doi.org/10.1021/ic000066v.

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41

Bessler, Karl E., Elisabeth B. Dourado, Myller de S. Carvalho, Sebastião S. Lemos, and Javier Ellena. "An Alternative Method for the Preparation of Diphenylboron Chelates. The Crystal and Molecular Structures of (Pyridine-2-acetyloximato)diphenylboron and (1-Phenylazo-2-naphtholato)diphenylboron." Zeitschrift für anorganische und allgemeine Chemie 631, no. 10 (2005): 1935–40. http://dx.doi.org/10.1002/zaac.200500192.

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42

Saha, Amrita, Partha Majumdar, Shie-Ming Peng, and Sreebrata Goswami. "Transition-Metal-Promoted C−N Bond-Formation Processes − Low-Spin FeIII, FeII, and NiII Complexes of 2-[(Arylamido)phenylazo]pyridine − X-ray Structure, Redox- and Spectroelectrochemistry." European Journal of Inorganic Chemistry 2000, no. 12 (2000): 2631–39. http://dx.doi.org/10.1002/1099-0682(200012)2000:12<2631::aid-ejic2631>3.0.co;2-k.

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43

Aviles Sanchez, Alejandro, Maryam Ghotbi, and Perla B. Balbuena. "Electron Transfer through Molecular Films for Neuromorphic Computing." ECS Meeting Abstracts MA2025-01, no. 63 (2025): 3069. https://doi.org/10.1149/ma2025-01633069mtgabs.

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The development of materials with neuromorphic behavior is essential for advancing computing hardware capable of mimicking biological neural networks. This work presents a comparative study of electron transfer mechanisms in thin films of two distinct types of materials with neuromorphic potential: (i) metal complexes such as [RuᴵᴵL₂](PF₆)₂, where L represents 2,6-bis(phenylazo)pyridine, and (ii) electroactive metal-organic frameworks (MOFs) like Zn²⁺-pyrazolate-based MOF with redox-active naphthalene diimide (NDI) groups, referred to as Zn(pyrazol-NDI) (where pyrazol-NDI = 1,4-bis[(3,5-dimeth
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44

Sheikhshoaie, Iran, and Vahid Saheb. "A new salen base 5-(phenylazo)-N-(2-amino pyridine) salicyliden Schiff base ligand: Synthesis, experimental and density functional studies on its crystal structure, FTIR, 1H NMR and 13C NMR spectra." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 77, no. 5 (2010): 1069–76. http://dx.doi.org/10.1016/j.saa.2010.08.075.

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Ackermann, Martin N., Carolyn R. Barton, Charles J. Deodene, et al. "Chromium, molybdenum, and tungsten zerovalent complexes of the nitrogen chelating ligand 2-(phenylazo)pyridine (2-PAP), including air-stable cis-M(CO)2(2-PAP)2 and M(2-PAP)3." Inorganic Chemistry 28, no. 3 (1989): 397–403. http://dx.doi.org/10.1021/ic00302a006.

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Rauth, Goutam Kumar, Sanjib Pal, Debasis Das, Chittaranjan Sinha, Alexander M. Z. Slawin, and J. Derek Woollins. "Synthesis, spectral characterization and electrochemical studies of mixed-ligand complexes of platinum(II) with 2-(arylazo)pyridines and catechols. Single-crystal X-ray structure of dichloro{2-(phenylazo) pyridine}platinum(II)." Polyhedron 20, no. 5 (2001): 363–72. http://dx.doi.org/10.1016/s0277-5387(00)00530-1.

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Zhu, Zhicheng, Masaaki Kojima, and Kiyohiko Nakajima. "Reversible ring opening and closure reactions of the triazine ligands derived from 1-phenylazo-2-naphthylamine and pyridine-2-aldehyde or quinoline-2-aldehyde – structure and reactivity of the palladium (II) complexes." Inorganica Chimica Acta 358, no. 3 (2005): 476–88. http://dx.doi.org/10.1016/j.ica.2004.08.024.

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Robertson, Jennifer J., Anders Kadziola, Ronald A. Krause, and Sine Larsen. "Preparation and characterization of four- and five-coordinate rhodium(I) complexes. Crystal structures of chloro(2-phenylazo)pyridine)(norbornadiene)rhodium(I), (2,2'-bipyridyl)(norbornadiene)rhodium(I) chloride hydrate, and chloro(2,2'-bipyridyl)(norbornadiene)rhodium(I)." Inorganic Chemistry 28, no. 11 (1989): 2097–102. http://dx.doi.org/10.1021/ic00310a017.

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Saha, Amrita, Partha Majumdar, and Sreebrata Goswami. "Low-spin manganese(II) and cobalt(III) complexes of N-aryl-2-pyridylazophenylamines: new tridentate N,N,N-donors derived from cobalt mediated aromatic ring amination of 2-(phenylazo)pyridine. Crystal structure of a manganese(II) complex †." Journal of the Chemical Society, Dalton Transactions, no. 11 (2000): 1703–8. http://dx.doi.org/10.1039/a909769d.

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Garza-Ortiz, Ariadna, Hans den Dulk, Jaap Brouwer, Huub Kooijman, Anthony L. Spek, and Jan Reedijk. "The synthesis, chemical and biological properties of dichlorido(azpy)gold(III) chloride (azpy=2-(phenylazo)pyridine) and the gold-induced conversion of the azpy ligand to the chloride of the novel tricyclic pyrido[2,1-c][1,2,4]benzotriazin-11-ium cation." Journal of Inorganic Biochemistry 101, no. 11-12 (2007): 1922–30. http://dx.doi.org/10.1016/j.jinorgbio.2007.05.008.

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