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	<dc:title xml:lang="en-US">Synthesis, crystal structure, and Hirshfeld surface analysis of a cubane-type tetranuclear polyoxotitanate cluster</dc:title>
	<dc:creator>Nath, Jayanta Kumar</dc:creator>
	<dc:subject xml:lang="en-US">Cubane</dc:subject>
	<dc:subject xml:lang="en-US">Carboxylic acids</dc:subject>
	<dc:subject xml:lang="en-US">Naphthalic anhydride</dc:subject>
	<dc:subject xml:lang="en-US">Polyoxotitanate cluster</dc:subject>
	<dc:subject xml:lang="en-US">Hirshfeld surface analysis</dc:subject>
	<dc:subject xml:lang="en-US">Supramolecular chemistry</dc:subject>
	<dc:description xml:lang="en-US">A cubane-type tetranuclear polyoxotitanate cluster derived from 8-(isopropoxycarbonyl)-1-naphthoic acid is reported which is synthesized under reflux conditions in isopropanol (HOiPr). The ligand 8-(isopropoxycarbonyl)-1-naphthoic acid (INA) was generated in situ from 1,8-naphthalic anhydride and isopropyl alcohol in the reaction mixture where one of the carboxylate groups of 1,8-naphthalene dicarboxylic acid (generated from the ring opening reaction of 1,8-naphthalic anhydride) forms isopropyl ester by reacting with solvent isopropoxide. The solid-state structural elucidation of the cluster is achieved through the single crystal X-ray diffraction method, providing detailed insights into their molecular arrangements. Crystal data for C72H80O24Ti4: Triclinic, space group P-1 (no. 2), a = 19.086(3) Å, b = 20.341(4) Å, c = 21.538(4) Å, α = 88.895(4)°, β = 72.158(4)°, γ = 89.049(4)°, V = 7958(3) Å3, Z = 4, T = 293(2) K, μ(MoKα) = 0.457 mm-1, Dcalc = 1.269 g/cm3, 64356 reflections measured (4.42° ≤ 2Θ ≤ 54.94°), 34455 unique (Rint = 0.0458, Rsigma = 0.0752) which were used in all calculations. The final R1 was 0.0603 (&amp;gt;2sigma(I)) and wR2 was 0.1558 (all data). In the crystal lattice, the asymmetric unit of the cluster contains two molecules. Various types of supramolecular interactions such as C-H···O, C-H···π, π···π and unusual O···O interactions are observed in the X-ray structures. All these interactions guide the formation of 3D supramolecular architecture in the solid state of the compound. In addition to these, 2D fingerprint (2D-FP) and Hirshfeld surface analysis (HSA) computations were used to prove and quantify various supramolecular interactions within the crystal lattice.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2025-06-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/2646</dc:identifier>
	<dc:identifier>10.5155/eurjchem.16.2.146-153.2646</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 16 No. 2 (2025): June 2025; 146-153</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/2646/2926</dc:relation>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/2646/2918</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2025 Jayanta Kumar Nath</dc:rights>
	<dc:rights xml:lang="en-US">https://creativecommons.org/licenses/by-nc/4.0</dc:rights>
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