Reactions of the arene-linked bis(pyrazolyl)methane ligands m-bis[bis(1-pyrazolyl)methyl]benzene, (m-[CH(pz)2]2C6H4, Lm), p-bis[bis(1-pyrazolyl)methyl]benzene, (p-[CH(pz)2]2C6H4, Lp), and 1,3,5-tris[bis(1-pyrazolyl)methyl]benzene (1,3,5-[CH(pz)2]3C6H3, L3) with AgX salts (pz = 1-pyrazolyl; X = BF4- or PF6-) yield two types of molecular motifs depending on the arrangement of the ligating sites about the central arene ring. Reactions of the m-phenylene-linked Lm with AgBF4 and AgPF6 afford complexes consisting of discrete, metallacyclic dications: [Ag2(mu-Lm)2](BF4)2 (1) and [Ag2(mu-Lm)2](PF6)2 (2). When the p-phenylene-linked Lp is treated with AgBF4 and AgPF6, acyclic, cationic coordination polymers are obtained: {[Ag(mu-Lp)]BF4}infinity (3) and {[Ag(mu-Lp)]PF6}infinity (4). Reaction of the ligand L3, containing three bis(pyrazolyl)methane units in a meta arrangement, with an equimolar amount of AgBF4 again yields discrete metallacyclic dications in which one bis(pyrazolyl)methane unit on each ligand remains unbound: [Ag2(mu-L3)2](BF4)2 (5). Treatment of L3 with an excess of AgBF4 affords a polymer of metallacycles, {[Ag3(mu-L3)2](BF4)3}infinity (6), with one of the bis(pyrazolyl)methane units on each ligand bound to a silver cation bridging two metallacycles. The supramolecular structures of the silver(I) complexes 1-6 are organized by noncovalent interactions, including weak hydrogen bonding, pi-pi, and anion-pi interactions.
The new ligands 1,1,4,4-tetra(1-pyrazolyl)butane [CH(pz)(2)(CH(2))(2)CH(pz)(2), L2] and 1,1,5,5-tetra(1-pyrazolyl)pentane [CH(pz)(2)(CH(2))(3)CH(pz)(2), L3] have been prepared to determine the structural changes in silver(I) complexes, if any, that accompany the lengthening of the spacer group between two linked bis(pyrazolyl)methane units. Silver(I) complexes of both ligands with BF(4)(-) and SO(3)CF(3)(-) as the counterion have the formula [Ag(2)(micro-L)(2)](counterion)(2). These complexes have a cyclic dimeric structure in the solid state previously observed with the shorter linked ligand CH(pz)(2)CH(2)CH(pz)(2). Similar chemistry starting with AgNO(3) for L2 yields a complex of the empirical formula [Ag(2)[micro-CH(pz)(2)(CH(2))(2)CH(pz)(2)](3)](NO(3))(2) that retains the cyclic dimeric structure, but bonding of an additional ligand creates a coordination polymer of the cyclic dimers. In contrast, coordination of the nitrate counterion to silver in the complex of L3 leads to the formation of the coordination polymer of the empirical formula [Ag(micro-CH(pz)(2)(CH(2))(3)CH(pz)(2))]NO(3). All six new complexes have extended supramolecular structures based on noncovalent interactions supported by the counterions and the functional groups designed into the ligands.
The new fixed-geometry, phenylene-linked bis(pyrazolyl)methane ligands α,α,α‘,α‘-tetra(1-pyrazolyl)-m-xylene (m-[CH(pz)2]2C6H4, L
m
), α,α,α‘,α‘-tetra(1-pyrazolyl)-p-xylene (p-[CH(pz)2]2C6H4, L
p
), and α,α,α‘,α‘-tetrakis(4-benzylpyrazol-1-yl)-p-xylene (p-[CH(4Bnpz)2]2C6H4,
4Bn
L
p
) have been synthesized in order to prepare hetero- and homobimetallic complexes
incorporating tricarbonylrhenium(I) and bis(p-tolyl)platinum(II) fragments. Coordination of
one rhenium center to L
m
was achieved to yield the monometallic rhenium complex {m-[CH(pz)2]2C6H4}Re(CO)3Br, which then incorporated a second metal center to give the heterobimetallic complex {μ-m-[CH(pz)2]2C6H4}[Re(CO)3Br][Pt(p-tolyl)2]. The homobimetallic rhenium complexes of each ligand, {μ-m-[CH(pz)2]2C6H4}[Re(CO)3Br]2, {μ-p-[CH(pz)2]2C6H4}[Re(CO)3Br]2, and {μ-p-[CH(4Bnpz)2]2C6H4}[Re(CO)3Br]2, were also prepared. The crystalline
structure of each complex shows extensive noncovalent interactions, including weak hydrogen
bonds and π···π and CH···π interactions, that organize the molecules into complex supramolecular structures.
The reaction of M(BF(4))(2).xH(2)O, where M is Fe, Co, Cu, and Zn, and the ditopic, bis(pyrazolyl)methane ligand m-[CH(pz)(2)](2)C(6)H(4), L(m), where pz is a pyrazolyl ring, yields the monofluoride bridged, binuclear [M(2)(mu-F)(mu-L(m))(2)](BF(4))(3) complexes. In contrast, a similar reaction of L(m) with Ni(BF(4))(2).6H(2)O yields dibridged [Ni(2)(mu-F)(2)(mu-L(m))(2)](BF(4))(2). The solid state structures of seven [M(2)(mu-F)(mu-L(m))(2)](BF(4))(3) complexes show that the divalent metal ion is in a five-coordinate, trigonal bipyramidal, coordination environment with either a linear or nearly linear M-F-M bridging arrangement. NMR results indicate that [Zn(2)(mu-F)(mu-L(m))(2)](BF(4))(3) retains its dimeric structure in solution. The [Ni(2)(mu-F)(2)(mu-L(m))(2)](BF(4))(2) complex has a dibridging fluoride structure that has a six-coordination environment about each nickel(II) ion. In the solid state, the [Fe(2)(mu-F)(mu-L(m))(2)](BF(4))(3) and [Co(2)(mu-F)(mu-L(m))(2)](BF(4))(3) complexes show weak intramolecular antiferromagnetic exchange coupling between the two metal(II) ions with J values of -10.4 and -0.67 cm(-1), respectively; there is no observed long-range magnetic order. Three different solvates of [Cu(2)(mu-F)(mu-L(m))(2)](BF(4))(3) are diamagnetic between 5 and 400 K, thus showing strong antiferromagnetic exchange interactions of -600 cm(-1) or more negative. Mossbauer spectra indicate that [Fe(2)(mu-F)(mu-L(m))(2)](BF(4))(3) exhibits no long-range magnetic order between 4.2 and 295 K and isomer shifts that are consistent with the presence of five-coordinate, high-spin iron(II).
Reactions of the arene-linked bis(pyrazolyl)methane ligands m-bis[bis(1-pyrazolyl)methyl]benzene (m-[CH(pz)2]2C6H4, Lm) and 1,3,5-tris[bis(1-pyrazolyl)methyl]benzene (1,3,5-[CH(pz)2]3C6H3, L3) with BF4- salts of divalent iron, zinc, and cadmium result in fluoride abstraction from BF4- and formation of fluoride-bridged metallacyclic complexes. Treatment of Fe(BF4)2.6H2O and Zn(BF4)2.5H2O with Lm leads to the complexes [Fe2(mu-F)(mu-Lm)2](BF4)3 (1) and [Zn2(mu-F)(mu-Lm)2](BF4)3 (2), in which a single fluoride ligand and two Lm molecules bridge the two metal centers. The reaction of [Cd2(thf)5](BF4)4 with Lm results in the complex [Cd2(mu-F)2(mu-Lm)2](BF4)2 (3), which contains dimeric cations in which two fluoride and two Lm ligands bridge the cadmium centers. Equimolar amounts of the tritopic ligand L3 and Zn(BF4)2.5H2O react to give the related monofluoride-bridged complex [Zn2(mu-F)(mu-L3)2](BF4)3 (4), in which one bis(pyrazolyl)methane unit on each ligand remains unbound. NMR spectroscopic studies show that in acetonitrile the zinc metallacycles observed in the solid-state remain intact in solution.
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