Self-assembly of tetra nuclear lanthanide (Pr, Nd) hydroxo clusters with functionalized β-diketone: Experimental and theoretical studies

被引:0
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作者
Jami, Ananda Kumar [1 ]
Kishore, Pilli V. V. N. [2 ]
Srinivasadesikan, Venkatesan [2 ]
Tripuramallu, Bharat Kumar [2 ]
Rao, Maddina Sreenivasa [3 ]
机构
[1] Godavari Global Univ, Dept Chem, Rajamahendravaram 533296, Andhra Pradesh, India
[2] Vignans Fdn Sci Technol & Res, Sch Appl Sci & Humanities, Dept Chem, Guntur 522213, India
[3] Godavari Global Univ, Dept Mech Engn, Rajamahendravaram 533296, Andhra Pradesh, India
关键词
Functionalization; beta-Diketones; Lanthanide hydroxo clusters; Structural topology; SINGLE-MOLECULE MAGNET; STRUCTURAL-CHARACTERIZATION; TRANS-A(2)B(2) PORPHYRINS; CRYSTAL-STRUCTURE; AMINO-ACIDS; COMPLEXES; COORDINATION; TETRANUCLEAR; LIGAND; REACTIVITY;
D O I
10.1016/j.poly.2024.117306
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of LnCl3 & sdot;6H2O (Ln = Pr, Nd) with functionalized beta-Diketone {ortho-hydroxydibenzoylmethane (HODBM)} in 1:2 ratio in methanol and in presence of triethylamine (excess) as base yielded two tetra nuclear lanthanide hydroxo clusters of composition [Ln4(O-DBM)4(HO-DBM)4(mu 3-OH)2][Et3NH]2.3CH2Cl2, (Ln = Pr (1), Nd (2)). The clusters 1 and 2 has been structurally characterized by single crystal X-ray diffraction. A onedimensional supramolecular chain is observed in the solid state structure (2), where dichloromethane solvent molecules are linked to the phenyl rings of adjacent diketone linkers through C-H & ctdot;pi and Cl & ctdot;pi interactions. Theoretical studies support the stability of structure (2), with calculated geometric parameters aligning with experimental findings.
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页数:7
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