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Relevant bibliographies by topics / 9-diaminononane

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Journal articles

Academic literature on the topic '9-diaminononane'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "9-diaminononane"

1

R., N. Prasad, and Gupta Nitin. "Template synthesis of Mnll complexes of tetraazamacrocycles derived from 2,3-butanedione and diaminoalkanes." Journal of Indian Chemical Society Vol. 82, Feb 2005 (2005): 140–42. https://doi.org/10.5281/zenodo.5824830.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, India <em>E-mail</em> : prasadraghtmandan@yahoo.com <em>Manuscript received 9 February 2004, revised 13 September 2004, accepted 17 September 2004 </em> Mn<sup>ll</sup> complexes of the type [MNL(NO<sub>3</sub>)<sub>2</sub>] (where L = macrocycle having 16 to 32-membered ring incorporating N<sub>4</sub> donor set) have been synthesized h the reactions of 2,3-butanedione with diaminoalkanes such as 1,4-diaminobutane, 1,5-diaminopentanc, 1,6- diaminolmexamme, 1,7-diaminolleptamme, 1,24-diaminooctane, 1,9-diaminononane, 1,10-d

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2

Reiß, Guido J., and Judith S. Engel. "Crystal Engineering of a New Layered Polyiodide Using 1,9-Diammoniononane as a Flexible Template Cation." Zeitschrift für Naturforschung B 59, no. 10 (2004): 1114–17. http://dx.doi.org/10.1515/znb-2004-1006.

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AbstractThe reaction of 1,9-diaminononane with hydroiodic acid in the presence of iodine gave a compound best described as 1,9-diammoniononane bis-triiodide iodine, (H3N-(CH2)9-NH3)[I3]2 · I2. The structure is built from two crystallographically independent I3− anions, which are connected via secondary I···I interactions to the iodine molecules, and the 1,9-diammonioalkane cations are connected via weak hydrogen bonds to neighbouring iodine atoms. By a cooperative phenomenon, the shape and the functionality of the cation lead to a solid state structure that includes a polyiodide substructure w

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3

Köferstein, Roberto. "Synthesis, Crystal Structure, Hydrogen Bonding, and Thermal Behavior of a Three-Dimensional CuII-benzene-1,2,4,5-tetracarboxylate Templated by 1,9-Diaminononane." Z. Anorg. Allg. Chem. 640 (April 16, 2014): 1937–42. https://doi.org/10.1002/zaac.201400177.

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Triclinic single crystals of Cu4(H3N–(CH2)9–NH3)(OH)2[C6H2(COO)4]2·5H2O were prepared in aqueous solution at 80 °C in the presence of 1,9-diaminononane. Space group P-1 (no. 2) with a = 1057.5(2), b = 1166.0(2), c = 1576.7(2) pm, alpha = 106.080(10)°, beta = 90.73(2)° and gamma = 94.050(10)°. The four crystallographic independent Cu2+ ions are surrounded by five oxygen atoms each with Cu–O distances between 191.4(3) and 231.7(4) pm. The connection between the Cu2+ coordination polyhedra and the [C6H2(COO)4]4– anions yields three-dimensional framew

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4

G., Indramahalakshmi, Thamaraichelvan A., and Gandhidasan R. "Inclusion Compounds Formed between Hofmann-(1,9-diaminononane)-type Host and Aromatic Guest." Asian Journal of Chemical Sciences 2, no. 4 (2017): 1–7. https://doi.org/10.9734/AJOCS/2017/34599.

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IR spectra of three tetracyanonickelate complexes with 1,9-diaminononane as ligand and three of their clathrates with guest nitrobenzene are presented. It is shown that they have similar structures and exhibit weak hydrogen bonding between the pi-electron cloud of aromatic guest and the ligand of the host lattice which is observed in all clathrates. A second type of hydrogen bonding is present between the NO<sub>2</sub> of nitrobenzene and the cyanide group of the lattice. The cyanide vibrational frequencies in the present clathrates are found to be in the order Cd-Ni-NB < Co-Ni-NB < Ni-

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5

R., N. Prasad, and Mathur Mala. "CrIII, FeIII, CoII, NiIII, CuIII and ZnIII complexes of 26- and 28-membered tetraazamacrocycles." Journal of Indian Chemical Society Vol. 83, Dec 2006 (2006): 1208–13. https://doi.org/10.5281/zenodo.5833937.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India <em>E-mail </em>: prasadraghunandan@yahoo.com <em>Manuscript received 17 June 2003, revised 11 September 2006, accepted 25 September 2006</em> 2+2 Cyclocondensation of 2,3-hexanedione with 1,9-diaminononane or 1,10-diaminodecane in the presence of metal ions as templates resulted in the formation of complexes of the types [ML(NO<sub>3</sub>)<sub>2</sub>]NO<sub>3</sub> {M = Cr<sup>III</sup>, Fe<sup>III</sup>}, [ML(NO<sub>3</sub>)<sub>2</sub>] {M = Co<sup>II</sup>, Ni<sup>II</sup>}, (CuL]CI<sub>2</sub> and (ZnLCl<

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6

Park, J. "Enzyme and reaction engineering to produce 9-aminononanoic acid, 1,9-nonanedioic acid, 1,9-nonanediol, 9-amino-1-nonanol, and 1,9-diaminononane from oleic acid to high yields." New Biotechnology 85 (March 2025): 177. https://doi.org/10.1016/j.nbt.2024.08.244.

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7

Kojima, Takahiko, Takeshi Usui, Morio Yashiro та ін. "Novel Carbinolamine Complex Derived from Ketomalonate and trans-[CoCl2(3,7-Diaza-1,9-diaminononane)]+. Synthesis and Characterization of [Co(N-(3,7-Diaza-9-aminononyl)-α-amino-α-hydroxymalonato)] ClO4·H2O". Chemistry Letters 20, № 1 (1991): 137–40. http://dx.doi.org/10.1246/cl.1991.137.

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8

Hwang, Se-Yeun, Ji-Min Woo, Go Eun Choi, Deok-Kun Oh, Joo-Hyun Seo, and Jin-Byung Park. "Biological Reaction Engineering for the Preparation of C9 Chemicals from Oleic Acid: 9-Aminononanoic Acid, 1,9-Nonanediol, 9-Amino-1-nonanol, and 1,9-Diaminononane." ACS Catalysis, March 4, 2024, 4130–38. http://dx.doi.org/10.1021/acscatal.4c00302.

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