Magnetic properties and magnetocaloric effect of Ln = Dy, Tb carborane-based metal-organic frameworks.

We present the synthesis and magneto-thermal properties of carborane-based lanthanide metal-organic frameworks (MOFs) with the formula {[(Ln)3(mCB-L)4(NO3)(DMF)n]·Solv}, where Ln = Dy or Tb, characterized by dc and ac susceptibility, X-ray absorption spectroscopy (XAS), X-ray magnetic circular dichroism (XMCD) and heat capacity measurements. The MOF structure is formed by polymeric 1D chains of Ln ions with three different coordination environments (Ln1, Ln2, Ln3) running along the b-axis, linked by carborane-based linkers thus to provide a 3D structure. Static magnetic measurements reveal that these MOFs behave at low temperature as a system of S* = 1/2 Ising spins, weakly interacting ferromagnetically along the 1D polymeric chain (J*/kB = +0.45 K (+0.5 K) interaction constant estimated for Dy-MOF (Tb-MOF)) and coupled to Ln ions in adjacent chains through dipolar antiferromagnetic interactions. The Dy MOF exhibits slow relaxation of magnetization through a thermally activated process, transitioning to quantum tunneling of the magnetization at low temperatures, while both compounds exhibit field-induced relaxation through a very slow, direct process. The maximum magnetic entropy changes (-ΔSmaxm) for an applied magnetic field change of 2-0 T are 5.71 J kg-1 K-1 and 4.78 J kg-1 K-1, for Dy and Tb MOFs, respectively, while the magnetocaloric effect (MCE) peak for both occurs at T ∼ 1.6 K, approximately double that for the Gd counterpart.

Switchable Surface Hydrophobicity-Hydrophilicity of a Metal-Organic Framework.

Materials with surfaces that can be switched from high/superhydrophobicity to superhydrophilicity are useful for myriad applications. Herein, we report a metal-organic framework (MOF) assembled from ZnII ions, 1,4-benzenedicarboxylate, and a hydrophobic carborane-based linker. The MOF crystal-surface can be switched between hydrophobic and superhydrophilic through a chemical treatment to remove some of the building blocks.

Binaphthyl platform as starting materials for the preparation of electron rich benzo[g,h,i]perylenes. Application to molecular architectures based on amino benzo[g,h,i]perylenes and carborane combinations.

Valuable amino benzo[g,h,i]perylenes have been obtained through a one pot electrophilic aromatic substitution--Scholl reaction sequence. Novel molecular architectures combining 3D-o-carborane and planar amino benzo[g,h,i]perylene units are described. Photophysical properties of amino benzo[g,h,i]perylene and the carborane-appended derivatives are discussed.

Self-assembly of halogenated cobaltacarborane compounds: boron-assisted C--H...X--B hydrogen bonds?

Full structural characterisation and complete synthetic procedures for three monohalogenated cobaltacarborane compounds closo-[3-Co(eta5-C5H5)-8-X-1,2-C2B9H10] (X=Cl (1), Br (2), I (3)) and the dibromo derivative closo-[3-Co(eta5-C5H5)-8,9-Br2-1,2-C2B9H9] (4) are reported. The supramolecular structures of 1, 3, and 4 reveal the existence of intermolecular C--HX--B interactions. The role of these interactions has been investigated through a CSD search and subsequent analysis of the reported crystalline compounds. The results show that halogens become reasonably good hydrogen-bond acceptors when bonded to boron and, in this respect, are comparable in strength to metal-bound halogens.

Generation and reactions of ruthenium phosphido complexes [(eta5-C5H5)Ru(PR'3)2(PR2)]: remarkably high phosphorus basicities and applications as ligands for palladium-catalyzed Suzuki cross-coupling reactions.

Reactions of [(eta5-C5H5)Ru(PR'3)2(Cl)] with NaBAr(F) [BAr(F)-=B{3,5-[C6H3(CF3)2]}4-; PR'3=PEt3 or 1/2Et2PCH2CH2PEt2) (depe)] and PR2H (R=Ph, a; tBu, b; Cy, c) in C6H5F, or of related cationic Ru(N2) complexes with PR2H in C6H5F, gave the secondary phosphine complexes [(eta5-C5H5)Ru(PR'3)2(PR2H)]+ BAr(F)- (PR'3=PEt3, 3 a-c; 1/2depe, 4 a,b) in 65-91 % yields. Additions of tBuOK (3 a, 4 a; [D6]acetone) or NaN(SiMe3)2 (3 b,c, 4 b; [D8]THF) gave the title complexes [(eta5-C5H5)Ru(PEt3)2(PR2)] (5 a-c) and [(eta5-C5H5)Ru(depe)(PR2)] (6 a,b) in high spectroscopic yields. These complexes were rapidly oxidized in air; with 5 a, [(eta5-C5H5)Ru(PEt3)2{P(=O)Ph2}] was isolated (>99 %). The reaction of 5 a and elemental selenium yielded [(eta5-C5H5)Ru(PEt3)2{P(=Se)Ph2}] (70 %); selenides from 5 c and 6 a were characterized in situ. Competitive deprotonation reactions showed that 5 a is more basic than the rhenium analog [(eta5-C5H5)Re(NO)(PPh3)(PPh2)], and that 6 b is more basic than PtBu3 and P(iPrNCH2CH2)3N. The latter is one of the most basic trivalent phosphorus compounds [pK(a)(acetonitrile) 33.6]. Complexes 5 a-c and 6 b are effective ligands for Pd(OAc)2-catalyzed Suzuki coupling reactions: 6 b gave a catalyst nearly as active as the benchmark organophosphine PtBu3; 5 a, with a less bulky and electron-rich PR2 moiety, gave a less active catalyst. The reaction of 5 a and [(eta3-C3H5)Pd(NCPh)2]+ BF4- gave the bridging phosphido complex [(eta5-C5H5)Ru(PEt3)2(PPh2)Pd(NCPh)(eta3-C3H5)]+ BAr(F)- in approximately 90 % purity. The crystal structure of 4 a is described, as well as substitution reactions of 3 b and 4 b.