Four 3D coordination polymers based on layers with single syn–anti carboxylate bridges: synthesis,structures, and magnetic properties

Four novel coordination polymers (CPs) based on a new 4-(3,5-dicarboxylphenyl) picolinic acid ligands (H₃L), [M₃(L)₂(H₂O)₆]·4H₂O (M₃ = Mn₃, 1; Co₃, 2; Ni₃, 3, Co_1.01Ni_1.99, 4), have been hydrothermally synthesized, and structurally and magnetically characterized. In these isomorphous CPs, octahedrally coordinated metal ions are linked by the single syn–anti carboxylate bridge (μ-COO) to give linear trinuclear motifs. The motifs are connected through the other single syn–anti carboxylate bridge (μ-COO) to give a 2D (4,4) layer, and the layers are interlinked by the L ligands into 3D frameworks. Magnetic measurement indicates that antiferromagnetic interactions between metal ions are mediated through the single syn–anti carboxylate bridges in 1 and 2, while the same carboxylate bridges in 3 transmit ferromagnetic couplings. The bimetallic CP 4 shows interesting complicated magnetic behaviors due to the competition effect of Co(ii) and Ni(ii) ions.

Four 3D carboxylate-bridged metal(II) compounds were prepared. Mn(II) and Co(II) compounds show AFM interactions, while FM coupling is found in Ni(II) compound. The bimetallic shows interesting competition effect of FM and AFM interactions.     

Comment on “Structural,electrical, and multiferroic characteristics of lead-free multiferroic: Bi(Co0.5Ti0.5)O3–BiFeO3 solid solution” by N. Kumar,A. Shukla,N. Kumar,R. Choudhary and A. Kumar,RSC Adv., 2018, 8, 36939”

My comments concern the significant errors in the crystallographic part of the commented paper. It was found that the studied crystal is of the sillenite type and the correct formula should be Bi₂₅FeO₃₉ : Co,Ti instead of BiFeO₃. Moreover, the type of unit cell is not correct. Due to the double doping the new type of unit cell, previously unknown, was proposed for such crystals. Furthermore, the authors did not find that the studied sample contains two slightly different phases, both of the sillenite type. The actual chemical composition of the studied crystals is not known.

The significant errors in the crystallographic part of the commented paper are described. The new chemical formula of the studied crystal is proposed: Bi₂₅FeO₃₉ : Co,Ti. The coexistence of two sillenite type phases is evidenced.     

A series of Ln4III clusters: Dy4 single molecule magnet and Tb4 multi-responsive luminescent sensor for Fe3+, CrO42−/Cr2O72− and 4-nitroaniline

Five tetranuclear lanthanide clusters of compositions [Ln₄L₄(NO₃)₂(Piv)₂]·2CH₃OH (Ln = Gd (1), Tb (2), Dy (3), Ho (4), Er (5); H₂L = 2-(((2-hydroxy-3-methoxybenzyl)imino)methyl)-6-methoxyphenol; Piv = pivalic acid) were synthesized under solvothermal conditions. The structures of 1–5 were characterized by single-crystal X-ray crystallography. Complexes 1–5 possess a zig-zag topology with [Ln₄O₆] cores being formed by the fusion of oxygen atom-bridged two [Ln₂O₂] moieties. Direct-current magnetic susceptibility studied in the 2–300 K range revealed weak antiferromagnetic interactions in 1, 2, 4, 5 and ferromagnetic interactions in 3. Complex 3 exhibits single molecule magnet (SMM) behavior. The luminescence studies indicated that complex 2 can serve as highly sensitive and selective luminescent materials for Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻ and 4-nitroaniline (4-NA), demonstrating that complex 2 should be a potential candidate for multi-responsive luminescent sensor.

Five tetranuclear lanthanide clusters were synthesized. Dy₄ complex exhibits single molecule magnet (SMM) behavior and Tb₄ compound shows sensing properties towards Fe³⁺, CrO₄²⁻, Cr₂O₇²⁻ and 4-nitroaniline (4-NA).     

Comment on “Metal–organic green dye: chemical and physical insight into a modified Zn-benzoporphyrin for dye-sensitized solar cells” by G. Zanotti,N. Angelini,G. Mattioli,A. M. Paoletti,G. Pennesi,G. Rossi,D. Caschera,L. de Marcoc and G. Giglide,RSC Adv., 2016, 6, 5123

The emission spectroscopy and photophysics reported in the title paper are shown to be untenable in light of previously reported experimental results and widely accepted theories of electronic excited state relaxation. The published results strongly suggest that the newly synthesized dye is contaminated with one of more highly fluorescent impurities.

The emission spectroscopy and photophysics reported in the title paper are shown to be untenable in light of previously reported experimental results and widely accepted theories of electronic excited state relaxation.