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Reference Reading

1.Understanding the electromagnetic interaction of metal organic framework reactants in aqueous solution at microwave frequencies.
Laybourn A1, Katrib J2, Palade PA2, Easun TL3, Champness NR4, Schröder M5, Kingman SW2. Phys Chem Chem Phys. 2016 Feb 10;18(7):5419-31. doi: 10.1039/c5cp05426e.
Preparation of metal organic frameworks (MOFs) via microwave heating is becoming increasingly popular due to reduced reaction times and enhanced control of MOF particle size. However, there is little understanding about the detailed interaction of the electric field portion of the wave with reactants during the synthesis of MOFs. In order to overcome this lack of fundamental understanding, information about the dielectric properties of the reactants is required. In this work the dielectric constants (ε') and loss factors (ε'') of benzene-1,4-dicarboxylic acid (H2BDC; also known as terephthalic acid) and a number of M(iii) (M = metal) salts dissolved in deionized water were measured as a function of frequency, temperature and concentration and with varying anions and cations. Dielectric data confirm the aqueous M(iii) salts to be strong microwave absorbers, particularly at 915 MHz. M(iii) salts with mono-anionic ligands (for example chlorides and nitrates) exhibit higher losses than di-anionic salts (sulfates) demonstrating that the former are heated more effectively in an applied microwave field.
2.Tuning Interchain Interactions in Two-Dimensional Networks of Mn(III) Schiff-Base Complexes and Dicarboxylic Acids by Varying the Linker.
Aono Y1, Yoshida H1, Katoh K1,2, Breedlove BK1,2, Kagesawa K1,2, Yamashita M1,2. Inorg Chem. 2015 Jul 20;54(14):7096-102. doi: 10.1021/acs.inorgchem.5b01154. Epub 2015 Jul 7.
Two-dimensional (2D) coordination polymers consisting of Mn(III) Schiff-base complexes and dicarboxylic acids, [{Mn(salen)}4(L1)](PF6)2·(CH3OH)2 (C4; H2L1 = adipid acid) and [{Mn(salen)}4(L2)](PF6)2·(CH3OH)4 (C4'; H2L2 = E,E-1,3-butadiene-1,4-dicarboxylic acid) (salen(2-) = N,N'-(ethylene)bis(salicylideneiminato), were synthesized by using a one-pot reaction and characterized by using single-crystal X-ray crystallographic analysis. One-dimensional (1D) chains composed of Mn(salen) dimers, [Mn2], bridged by carboxylato ligands (-[Mn2]-OCO--[Mn2]-), were linked by dicarboxylato ligands with n-butyl (-C4H8-) (C4) and butadienyl aliphatic groups (-C4H4-) (C4'). From static magnetic measurements on both C4 and C4', there were ferromagnetic interactions between the Mn(III) ions through the phenoxo oxygen atoms of the salen(2-), and antiferromagnetic interactions between the Mn(III) ions through carboxylato ligands (-OCO-). As a result, weak ferromagnetism occurred because of the zigzag-shaped chain structure of C4 and C4', and magnetic anisotropy for Mn(salen).
3.Novel nanorose-like Ce(iii)-doped and undoped Cu(ii)-biphenyl-4,4-dicarboxylic acid (Cu(ii)-BPDCA) MOSs as visible light photocatalysts: synthesis, characterization, photodegradation of toxic dyes and optimization.
Mousavinia SE1, Hajati S1, Ghaedi M2, Dashtian K2. Phys Chem Chem Phys. 2016 Apr 7. [Epub ahead of print]
A novel nanorose-like metal organic system (MOS) based on Cu(ii) and biphenyl-4,4-dicarboxylic acid (Cu-BPDCA) was hydrothermally synthesized and characterized via EDS, FE-SEM, XRD, DRS and FT-IR analysis. This novel nanomaterial was found to be of narrow energy band gap (1.24 eV) and thus it was applied as a photocatalyst driven by visible light for the degradation of the rose bengal (RB) and eosin Y (EY) dyes. For further improvement in the photocatalytic performance of Cu-BPDCA, it was doped with a trace amount of Ce(iii) in a simple way followed by characterization. The achieved improvement is due to the formation of a large number of O2-˙ and ˙OH radicals compared to the case of undoped Cu-BPDCA. The influence of important variables such as initial dye concentration, photocatalyst dosage and time of irradiation on the photocatalytic degradation efficiency was studied and optimized using central composite design. The optimum condition for the photodegradation of RB was found to be 40 min, 4.
4.Synthesis and optical power limiting properties of heteroleptic Mo3S7 clusters.
Recatalá D1, Llusar R, Barlow A, Wang G, Samoc M, Humphrey MG, Guschin AL. Dalton Trans. 2015 Aug 7;44(29):13163-72. doi: 10.1039/c5dt01244a.
Substitution of the halide ligands in (Bu4N)2[Mo3S7X6] (X = Cl, Br) by diimine ligands, such as 4,4'-dimethyl-2,2'-bipyridine (dmbpy), 2,2'-bipyridine (bpy) and 1,10-phenanthroline (phen), affords the neutral heteroleptic clusters Mo3S7Cl4(dmbpy) (), Mo3S7Br4(dmbpy) (), Mo3S7Br4(bpy) (), and Mo3S7Br4(phen) (). Further substitution of the halide ligands in Mo3S7Br4(diimine) clusters by dmit (1,3-dithiole-2-thione-4,5-dithiolate) allows the preparation of the mixed diimine-dithiolene neutral cluster complexes Mo3S7(dnbpy)(dmit)2 (, dnbpy = 4,4'-dinonyl-2,2'-bipyridine), Mo3S7(dcmbpy)(dmit)2 (, dcmbpy = 4,4'-dimethoxycarbonyl-2,2'-bipyridine), and Mo3S7(dcbpy)(dmit)2 (, dcbpy = 2,2'-bipyridine-4,4'-dicarboxylic acid). The optical limiting properties of complexes have been assessed by the open-aperture Z-scan technique at 570 nm, employing a nanosecond optical parametric oscillator. In order to investigate the effect of increasing the π-system, complexes , with the general formula Mo3S7X4(diimine), (X = Cl, Br), were compared to clusters , containing the dmit ligand.