Relevant bibliographies by topics / 2-hydroxy-1-naphthaldehyde

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Academic literature on the topic '2-hydroxy-1-naphthaldehyde'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "2-hydroxy-1-naphthaldehyde"

1

Lovejoy, David B., Des R. Richardson, and Paul V. Bernhardt. "2-Hydroxy-1-naphthaldehyde 2-methylthiosemicarbazone." Acta Crystallographica Section C Crystal Structure Communications 56, no. 3 (2000): 341–42. http://dx.doi.org/10.1107/s0108270199015140.

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Maniukiewicz, W., and M. Bukowska-Strzyżewska. "Structure of 2-hydroxy-1-naphthaldehyde." Acta Crystallographica Section C Crystal Structure Communications 48, no. 7 (1992): 1324–26. http://dx.doi.org/10.1107/s0108270191013628.

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Ahmed, Ahmed Ibrahim, and Enaam Ismail Yousif. "New Metal Complexes with AZO ligand; Synthesis, Spectral Characterisation and Biological Evaluation." Pakistan Journal of Medical and Health Sciences 16, no. 7 (2022): 550–53. http://dx.doi.org/10.53350/pjmhs22167550.

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The new Azo ligand and its metal complexes have been prepared and characterized The reaction of 4-nitroaniline and 2-hydroxy-1-naphthaldehyde in a 1:1 mole ratio resulted in the synthesis of ((E)-2-hydroxy-3-((4-nitrophenyl) diazenyl)-1-naphthaldehyde) (HL). The separation of monomeric complexes was accomplished by reacting ((E)-2-hydroxy-3-((4-nitrophenyl)diazenyl)-1-naphthaldehyde) (HL) with Cr, Mn II, Co II, Ni II, and Cu II metal ions in a mole ratio of 2:1 (L: M). Elemental microanalysis, magnetic susceptibility, conductance, FT-IR, electronic spectra, and 1HNMR, 13C-NMR, and mass spectra
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Zhu, Li-Na, Chang-Qing Li, Xiao-Zeng Li, and Rong Li. "Bis(2-hydroxy-1-naphthaldehyde) oxaloyldihydrazone dihydrate." Acta Crystallographica Section E Structure Reports Online 62, no. 10 (2006): o4603—o4605. http://dx.doi.org/10.1107/s1600536806037615.

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Narang, Krishan K., and Meena K. Singh. "Polymeric complexes of bivalent transition metal ions with 2-hydroxy-1-naphthaldehyde oxaldihydrazone and 2-hydroxy-1-naphthaldehyde malondihydrazone." Transition Metal Chemistry 12, no. 5 (1987): 385–88. http://dx.doi.org/10.1007/bf01171642.

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Valdés-Martínez, Jesús, Simón Hernández-Ortega, and Victor Bautista Jimenez. "Ammine[2-hydroxy-1-naphthaldehyde 4-piperidylthiosemicarbazonato]nickel(II)." Acta Crystallographica Section E Structure Reports Online 58, no. 12 (2002): m710—m711. http://dx.doi.org/10.1107/s1600536802020184.

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7

Chowdhury, Papia, Subhasis Panja, and Sankar Chakravorti. "Excited State Prototropic Activities in 2-Hydroxy 1-Naphthaldehyde." Journal of Physical Chemistry A 107, no. 1 (2003): 83–90. http://dx.doi.org/10.1021/jp026404q.

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Martínez, R. Fernando, Martín Ávalos, Reyes Babiano, et al. "Tautomerism in Schiff bases. The cases of 2-hydroxy-1-naphthaldehyde and 1-hydroxy-2-naphthaldehyde investigated in solution and the solid state." Organic & Biomolecular Chemistry 9, no. 24 (2011): 8268. http://dx.doi.org/10.1039/c1ob06073b.

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9

Huang, Jing, Lei Yang, Minglian Fu, Zhangxu Chen, and Xiaojin Huang. "Theoretical investigations on the excited-state intramolecular proton transfer in the solvated 2-hydroxy-1-naphthaldehyde carbohydrazone." Open Chemistry 20, no. 1 (2022): 785–92. http://dx.doi.org/10.1515/chem-2022-0199.

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Abstract The vast applications of 2-hydroxy-1-naphthaldehyde-derived systems in the sensors originate from their unusual excited-state intramolecular proton transfer (ESIPT) fluorescence in the molecules. The mechanism of ESIPT fluorescence in the solvated 2-hydroxy-1-naphthaldehyde carbohydrazone (HNLSC) system was investigated by ab initio time-dependent density functional theory (TDDFT) calculation. The solvation stabilized both ground state and excited state in the enol form, and the medium intramolecular interaction ensured the bond break, bond-forming and proton transfer in the conversio
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You, Zhong-Lu, Jia Wang, and Jing-Yun Chi. "4-{[(2-Hydroxy-1-naphthyl)methylidene]amino}-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (2006): o1652—o1653. http://dx.doi.org/10.1107/s160053680601110x.

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The title compound, C22H19N3O2, is a Schiff base compound derived from 4-aminoantipyrine and 2-hydroxy-1-naphthaldehyde. As expected, the two crystallographically independent molecules adopt trans configurations about the central C=N bonds.
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Book chapters on the topic "2-hydroxy-1-naphthaldehyde"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_111.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxomolybdenum(V) complex with hydrazone derived from 6-methyl-4-hydroxy-2- hydrazinopyrimidine and 2-hydroxy-1-naphthaldehyde." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_558.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of tetraaqua-[bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazonato]cobalt(II)-copper(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_252.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of tetraaqua-[bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazonato]oxomolybdenum(VI)-copper(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_153.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of tetraaqua-[bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazonato]manganese(II)-copper(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_216.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterobimetallic Ni(II)-Cu(II) complex with bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_89.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterobimetallic UO2(VI)-Cu(II) complex with bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_444.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterobimetallic Zn(II)-Cu(II) complex with bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_280.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of homobimetallic Cu(II)-Cu(II) complex with bis(2-hydroxy-1-naphthaldehyde)malonoyldihydrazone." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_183.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of manganese(III) complex with Schiff-base derived from 2-hydroxy-1-naphthaldehyde and glycine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_356.

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Journal articles
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