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1.
The reactions of [M(II)(Tpm(Me))(H2O)3]2+ (M = Ni, Co, Fe; Tpm(Me) = tris(3,5-dimethyl-1-pyrazoyl)methane) with [Bu4N][(Tp)Fe(III)(CN)3] (Bu4N+ = tetrabutylammonium cation; Tp = tris(pyrazolyl)hydroborate) in MeCN-Et2O afford three pentanuclear cyano-bridged clusters, [(Tp)3(Tpm(Me))2Fe(III)3M(II)2(CN)9]ClO4.15H2O (M = Ni, 1; M = Co, 2) and [(Tp)3(Tpm(Me))2Fe(III)3Fe(II)2(CN)9]BF4.15H2O (3). Single-crystal X-ray analyses reveal that they show the same trigonal bipyramidal structure featuring a D3h-symmetry core, in which two opposing Tpm(Me)-ligated M(II) ions situated in the two apical positions are linked through cyanide bridges to an equatorial triangle of three Tp-ligated Fe(III) (S = 1/2) centers. Magnetic studies for complex 1 show ferromagnetic coupling giving an S = 7/2 ground state and an appreciable magnetic anisotropy with a negative D(7/2) value equal to -0.79 cm(-1). Complex 2 shows zero-field splitting parameters deducted from the magnetization data with D = -1.33 cm(-1) and g = 2.81. Antiferromagnetic interaction was observed in complex 3. 相似文献
2.
Miyasaka H Takahashi H Madanbashi T Sugiura K Clérac R Nojiri H 《Inorganic chemistry》2005,44(17):5969-5971
Two cyano-bridged tetranuclear complexes composed of Mn(III) salen (salen = N,N'-ethylene bis(salicylideneiminate)) and hexacyanometalate(III) (M = Fe, Cr) in a stoichiometry of 3:1 have been selectively synthesized using {NH2(n-C12H25)2}3[M(III)(CN)6] (M(III) = Fe, Cr) starting materials: [{Mn(salen)(EtOH)}3{M(CN)6}] (M = Fe, 1; Cr, 2). Compounds 1 and 2 are isostructural with a T-shaped structure, in which [M(CN)6]3- assumes a meridional-tridentate building block to bind three [Mn(salen)(EtOH)]+ units. The strong frequency dependence and observation of hysteresis on the field dependence of the magnetization indicate that 1 is a single-molecule magnet. 相似文献
3.
Self-assembly of a new precursor [Cu(L)](ClO4)2 (1) (L = macrocyclic ligand) with octacyanometalates [M(CN)8]3- (M = Mo, W) produced two-dimensional cyano-bridged Cu(II)-M(V) bimetallic assemblies [Cu(L)]3n[M(CN)8]2n.6nH2O [M = Mo (2), W (3)] with novel honeycomblike structures, characterized by spectroscopic data, single-crystal X-ray diffraction studies, and magnetic measurements. The crystallographic determination reveals that compounds 2 and 3 are isostructural and crystallize in the triclinic system (P). The Cu atom in a distorted octahedral environment experiences a tetragonal elongation of apical nitrogen atoms exhibiting average Cu-Nax lengths of 2.566 Angstroms for 2 and 2.593 Angstroms for 3, which accounts for the Jahn-Teller effect of a Cu(II) ion. The Cu-NC angles are magnetically important, ranging from 135.7 to 159.2 degrees. Three types of L in the crystal lattice are observed, which are dependent on the relative positions of the pendant hydroxyl groups with respect to the CuN4 basal plane. The positions are correlated with hydrogen bonding of OH groups to neighboring atoms. The magnetic data indicate that ferromagnetic and antiferromagnetic interactions between Cu(II) and M(V) through the CN linkage coexist. 相似文献
4.
Colacio E Ghazi M Stoeckli-Evans H Lloret F Moreno JM Pérez C 《Inorganic chemistry》2001,40(19):4876-4883
Reactions between [M(N(4)-macrocycle)](2+) (M = Zn(II) and Ni(II); macrocycle ligands are either CTH = d,l-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane or cyclam = 1,4, 8, 11-tetrazaazaciclotetradecane) and [M(CN)(6)](3-) (M = Fe(III) and Mn(III)) give rise to cyano-bridged assemblies with 1D linear chain and 2D honeycomblike structures. The magnetic measurements on the 1D linear chain complex [Fe(cyclam)][Fe(CN)(6)].6H(2)O 1 points out its metamagnetic behavior, where the ferromagnetic interaction operates within the chain and the antiferromagnetic one between chains. The Neel temperature, T(N), is 5.5 K and the critical field at 2 K is 1 T. The unexpected ferromagnetic intrachain interaction can be rationalized on the basis of the axially elongated octahedral geometry of the low spin Fe(III) ion of the [Fe(cyclam)](3+) unit. The isostructural substitution of [Fe(CN)(6)](3-) by [Mn(CN)(6)](3-) in the previously reported complex [Ni(cyclam)](3)[Fe(CN)(6)](2).12H(2)O 2 leads to [Ni(cyclam)](3)[Mn(CN)(6)](2).16 H(2)O 3, which exhibits a corrugated 2D honeycomblike structure and a metamagnetic behavior with T(N) = 16 K and a critical field of 1 T. In the ferromagnetic phase (H > 1 T) this compound shows a very important coercitive field of 2900 G at 2 K. Compound [Ni(CTH)](3)[Fe(CN)(6)](2).13H(2)O 4, C(60)H(116)Fe(2)N(24)Ni(3)O(13), monoclinic, A 2/n, a = 20.462(7), b = 16.292(4), c = 27.262(7) A, beta = 101.29(4) degrees, Z = 4, also has a corrugated 2D honeycomblike structure and a ferromagnetic intralayer interaction, but, in contrast to 2 and 3, does not exhibit any magnetic ordering. This fact is likely due to the increase of the interlayer separation in this compound. ([Zn(cyclam)Fe(CN)(6)Zn(cyclam)] [Zn(cyclam)Fe(CN)(6)].22H(2)O.EtOH) 5, C(44)H(122)Fe(2)N(24)O(23)Zn(3), monoclinic, A 2/n, a = 14.5474(11), b = 37.056(2), c = 14.7173(13) A, beta = 93.94(1) degrees, Z = 4, presents an unique structure made of anionic linear chains containing alternating [Zn(cyclam)](2+) and [Fe(CN)(6)](3)(-) units and cationic trinuclear units [Zn(cyclam)Fe(CN)(6)Zn(cyclam)](+). Their magnetic properties agree well with those expected for two [Fe(CN)(6)](3-) units with spin-orbit coupling effect of the low spin iron(III) ions. 相似文献
5.
Colacio E Costes JP Domínguez-Vera JM Maimoun IB Suárez-Varela J 《Chemical communications (Cambridge, England)》2005,(4):534-536
The first examples of azide-bridged bimetallic trinuclear complexes ([M(cyclam)][FeL(N3)(mu1,5-N3)]2) (H2L = 4,5-dichloro-1,2-bis(pyridine-2-carboxamido) benzene) have been structurally and magnetically characterized. 相似文献
6.
Two cyano-bridged Cu(II)-M(V) [M = Mo (2), W (3)] complexes formed by self-assembly of octacyanometalates [M(CN)8]3- (M = Mo, W) with a new molecular precursor [Cu(L2)]2+ (1) (L2 = a macrocyclic ligand) in a 2:3 ratio have been investigated in terms of structures and magnetic behaviors. The M2Cu3 repeating unit of both bimetallic compounds is extended to a two-dimensional honeycomblike layered structure. The pendant ethyl groups on L2 noticeably influence the structural parameters around the Cu center. Compared with the system composed of a macrocycle without a side group, Cu-N(ax) (ax = axial) distances become shorter and the Cu-N(ax)-C(ax) angles are more bent for 2 and 3. The magnetic data denote that the Cu(II) and M(V) spins undergo explicit ferromagnetic interactions via CN bridges. From a structural and magnetic point of view, given that the Cu-N(ax) bond length in the tetragonally distorted octahedral Cu(II) environment is long enough, the overall ferromagnetic character remains despite the variation of Cu-N(ax)-C(ax) angle in this system. 相似文献
7.
Two cyano-bridged bimetallic complexes {[M2(H2O)4Mo(CN)8] · 4H2O}
n
[M = Mn (I) and Co (II)] have been synthesized and structurally characterized. The single-crystal X-ray analyses reveal that
these two compounds have three-dimensional structures, and cell parameters are similar in a tetragonal system with space group
I
$
\bar 4
$
\bar 4
. In the both complexes, each [Mo(CN)8]4− building block is linked with M2+ [M = Mn and Co] ions through its eight CN ligands. Each M2+ center is connected to four Mo units forming a three-dimensional framework. In addition, magnetic studies of these complexes
have been presented. 相似文献
8.
The dinucleating macrocyclic ligands (L(2;2))(2-) and (L(2;3))(2-), comprised of two 2-[(N-methylamino)methyl]-6-(iminomethyl)-4-bromophenolate entities combined by the -(CH(2))(2)- chain between the two aminic nitrogen atoms and by the -(CH(2))(2)- or -(CH(2))(3)- chain between the two iminic nitrogen atoms, have afforded the following M(II)Cu(II) complexes: [CoCu(L(2;2))](ClO(4))(2).MeCN (1A), [NiCu(L(2;2))](ClO(4))(2) (2A), [ZnCu(L(2;2))](ClO(4))(2).0.5MeCN.EtOH (3A), [CoCu(L(2;3))(MeCN)(2-PrOH)](ClO(4))(2) (4A), [NiCu(L(2;3))](ClO(4))(2) (5A), and [ZnCu(L(2;3))](ClO(4))(2).1.5DMF (6A). [CoCu(L(2;2))(MeCN)(3)](ClO(4))(2) (1A') crystallizes in the monoclinic space group P2(1)/n, a = 11.691(2) A, b = 18.572(3) A, c = 17.058(3) A, beta= 91.18(2) degrees, V = 3703(1) A(3), and Z = 4. [NiCu(L(2;2))(DMF)(2)](ClO(4))(2) (2A') crystallizes in the triclinic space group P(-)1, a = 11.260(2) A, b = 16.359(6) A, c = 10.853(4) A, alpha= 96.98(3) degrees, beta= 91.18(2) degrees, gamma= 75.20(2) degrees, V = 1917(1) A(3), and Z = 2. 4A crystallizes in the monoclinic space group P2(1)/c, a = 15.064(8) A, b = 11.434(5) A, c = 21.352(5) A, beta= 95.83(2)degrees, V = 3659(2) A(3), and Z = 4. The X-ray crystallographic results demonstrate the M(II) to reside in the N(amine)(2)O(2) site and the Cu(II) in the N(imine)(2)O(2) site. The complexes 1-6 are regarded to be isomeric with [CuCo(L(2;2)))](ClO(4))(2).DMF (1B), [CuNi(L(2;2)))](ClO(4))(2).DMF.MeOH (2B), [CuZn(L(2;2)))](ClO(4))(2).H(2)O (3B)), [CuCo(L(2;3)))](ClO(4))(2).2H(2)O (4B), [CuNi(L(2;3)))](ClO(4))(2) (5B), and [CuZn(L(2;3)))](ClO(4))(2).H(2)O (6B) reported previously, when we ignore exogenous donating and solvating molecules. The isomeric M(II)Cu(II) and Cu(II)M(II) complexes are differentiated by X-ray structural, magnetic, visible spectroscopic, and electrochemical studies. The two isomeric forms are significantly stabilized by the "macrocyclic effect" of the ligands, but 1A is converted into 1B on an electrode, and 2A is converted into 2B at elevated temperature. 相似文献
9.
Four octacyanometalate-based bimetallic Cu-M (M = Mo, W) assemblies coordinated by tetradentate macrocyclic ligands were prepared via self-assembly process in a stoichiometric ratio of [M(CN)8]3- and Cu(macrocycle)2+ and characterized in terms of structures and magnetic properties. The crystal structures are varied depending on the macrocycles used. The employment of cyclam with no pendant groups produced a one-dimensional chain (1) with a rope-ladder pattern, whereas macrocycles with side groups allowed for the formation of two-dimensional honeycomb-like architectures (2-4). From the crystal structures, the variations in apical Cu-Nax lengths and Cu-Nax-Cax angles on the bridging pathways are observed, which arises from the existence of side groups on macrocyclic ligands. The magnetic results reveal that all of the prepared compounds show ferromagnetic couplings between magnetic centers transimitted through CN bridges under the present structural parameters. Comparing the magnetic strength of the Cu-Mo (3d-4d; 2) and Cu-W (3d-5d; 3) complexes supports that 3d-5d magnetic coupling is stronger than 3d-4d because the 5d orbital is more diffuse than 4d. The magnetic analyses for 1-4 and related complexes tentatively suggest that, when the Cu-Nax distances are long enough, the axial Cu-Nax bond length in the bridging route may be one of the major structural parameters to determine the magnitude of the ferromagnetic exchange coupling. 相似文献
10.
Two unique cyano-bridged 2D coordination polymers have been synthesized and characterized structurally and magnetically. The complexes contain two polyaza Cu(II) units and one novel macromolecular Cu(II) moiety, which have been synthesized via one-pot metal template condensation reactions involving ethylenediamine (en) and formaldehyde. Self-assembly of the polyaza Cu(II) mixture with [Cr(CN)(6)](3)(-) gave rise to two layered complexes. One complex contains unprecedented covalently linked polymeric Cu(II) chains and cyano-bridged Cu(II)(-)Cr(III) coordination chains, which are interwoven to form a novel layer. The other complex shows intriguing encapsulation of [Cr(CN)(6)](3)(-) anions. Intermetallic ferromagnetic coupling is operative within the bridged 2D layer. The magnetic susceptibilities of both complexes were simulated using approximate models. 相似文献
11.
Toma LM Delgado FS Ruiz-Pérez C Carrasco R Cano J Lloret F Julve M 《Dalton transactions (Cambridge, England : 2003)》2004,(18):2836-2846
The bimetallic complexes [[Fe(III)(phen)(CN)4]2Cu(II)(H2O)2].4H2O (1), [[Fe(III)(phen)(CN)4]2Cu(II)].H2O (2) and [[Fe(III)(bipy)(CN)4]2Cu(II)].2H2O (3) and [[Fe(III)(bipy)(CN)4]2Cu(II)(H2O)2].4H2O (4) (phen = 1,10-phenanthroline and bipy = 2,2'-bipyridine) have been prepared and the structures of 1-3 determined by X-ray diffraction. The structure of 1 is made up of neutral cyanide-bridged Fe(III)-Cu(II) zigzag chains of formula [[Fe(III)(phen)(CN)4]2Cu(II)(H2O)2] and uncoordinated water molecules with the [Fe(phen)(CN)4]- entity acting as a bis-monodentate bridging ligand toward two trans-diaquacopper(II) units through two of its four cyanide groups in cis positions. The structure of 2 can be viewed as the condensation of two chains of 1 connected through single cyanide-bridged Fe(III)-Cu(II) pairs after removal of the two axially coordinated water molecules of the copper atom. The structure of 3 is like that of 2, the main differences being the occurrence of bipy (phen in 2) and two (one in 2) crystallization water molecules. The crystals of 4 diffract poorly but the analysis of the limited set of diffraction data shows a chain structure like that of 1 the most important difference being the fact that elongation axis at the copper atom is defined by the two trans coordinated water molecules. 1 behaves as a ferromagnetic Fe(III)2Cu(II) trinuclear system. A metamagnetic-like behavior is observed for 2 and 3, the value of the critical field (Hc) being ca. 1100 (2) and 900 Oe (3). For H > Hc the ferromagnetic Fe(III)2Cu(II) chains exhibit frequency dependence of the out-of-phase ac susceptibility signal at T < 4.0 K. The magnetic behavior of 4 corresponds to that of a ferromagnetically coupled chain of low spin iron(III) and copper(II) ions with frequency dependence of the out-of-phase susceptibility at T < 3.0 K. Theoretical calculations using methods based on density functional theory (DFT) have been employed to analyze and substantiate the exchange pathways in this family of complexes. 相似文献
12.
Toma L Toma LM Lescouëzec R Armentano D De Munno G Andruh M Cano J Lloret F Julve M 《Dalton transactions (Cambridge, England : 2003)》2005,(8):1357-1364
The binuclear complex NiII2L(H2O)2(ClO4)2(1) and the neutral tetranuclear bimetallic compounds [{M(III)(phen)(CN)4}2{NiII2L(H2O)2}].2CH3CN with M=Fe (2) and Cr (3)[H2L=11,23-dimethyl-3,7,15,19-tetraazatricyclo[19.3.1.1(9,13)]hexacosa-2,7,9,11,13(26),14,19,21(25),22,24-decaene-25,26-diol] have been synthesized and the structures of and determined by single crystal X-ray diffraction. and are isostructural compounds whose structure is made up of centrosymmetric binuclear cations [Ni2(L)(H2O)2]2+ and two peripheral [M(phen)(CN)4]- anions [M=Fe (2) and Cr (3)] acting as monodentate ligands towards the nickel atoms through one of their four cyanide nitrogen atoms. The environment of the metal atoms in 2 and 3 is six-coordinated: two phen-nitrogen and four cyanide-carbon atoms at the iron and chromium atoms and a water molecule, one cyanide-nitrogen and two phenolate-oxygens and two imine-nitrogens from the binucleating ligand L2- at the nickel atom build distorted octahedral surroundings. The values of the FeNi and CrNi separations through the single cyanide bridge are 5.058(1) and 5.174(2)A respectively, whereas the Ni-Ni distances across the double phenolate bridge are 3.098(2)(2) and 3.101(1) A (3). The magnetic properties of have been investigated in the temperature range 1.9-290 K. The magnetic behaviour of corresponds to that of an antiferromagnetically coupled nickel(II) dimer with J=-61.0(1) cm-1, the Hamiltonian being defined as H=-J S(A).S(B). An overall antiferromagnetic behaviour is observed for and with a low-lying singlet spin state. The values of the intramolecular magnetic couplings are J(Fe-Ni)=+17.4(1) cm-1 and J(Ni-Ni(a))=-44.4(1) cm-1 for and J(Cr-Ni)=+11.8(1) cm-1 and J(Ni-Ni(a))=-44.6(1) cm-1 for [H=-J(M-Ni)(S(M).S(Ni)+S(Ma).S(Nia))-J(Ni-Nia)S(Ni)S(Nia)]. Theoretical calculations using methods based on density functional theory (DFT) have been employed on in order to analyze the efficiency of the exchange pathways involved and also to substantiate the exchange coupling parameters. 相似文献
13.
Cyano-bridged Mn(III)-M(III) single-chain magnets with M(III)=Co(III), Fe(III), Mn(III), and Cr(III)
Miyasaka H Madanbashi T Saitoh A Motokawa N Ishikawa R Yamashita M Bahr S Wernsdorfer W Clérac R 《Chemistry (Weinheim an der Bergstrasse, Germany)》2012,18(13):3942-3954
A series of isostructural cyano-bridged Mn(III)(h.s.)-M(III)(l.s.) alternating chains, [Mn(III)(5-TMAMsalen)M(III)(CN)(6)]?4H(2)O (5-TMAMsalen(2-)=N,N'-ethylenebis(5-trimethylammoniomethylsalicylideneiminate), Mn(III)(h.s.)=high-spin Mn(III), M(III)(l.s.)=low-spin Co(III), Mn-Co; Fe(III), Mn-Fe; Mn(III), Mn-Mn; Cr(III), Mn-Cr) was synthesized by assembling [Mn(III)(5-TMAMsalen)](3+) and [M(III)(CN)(6)](3-). The chains present in the four compounds, which crystallize in the monoclinic space group C2/c, are composed of an [-Mn(III)-NC-M(III)-CN-] repeating motif, for which the -NC-M(III)-CN- motif is provided by the [M(III)(CN)(6)](3-) moiety adopting a trans bridging mode between [Mn(III)(5-TMAMsalen)](3+) cations. The Mn(III) and M(III) ions occupy special crystallographic positions: a C(2) axis and an inversion center, respectively, forming a highly symmetrical chain with only one kind of cyano bridge. The Jahn-Teller axis of the Mn(III)(h.s.) ion is perpendicular to the N(2)O(2) plane formed by the 5-TMAMsalen tetradentate ligand. These Jahn-Teller axes are all perfectly aligned along the unique chain direction without a bending angle, although the chains are corrugated with an Mn-N(axis) -C angle of about 144°. In the crystal structures, the chains are well separated with the nearest inter-chain M???M distance being relatively large at 9?? due to steric hindrance of the bulky trimethylammoniomethyl groups of the 5-TMAMsalen ligand. The magnetic properties of these compounds have been thoroughly studied. Mn-Fe and Mn-Mn display intra-chain ferromagnetic interactions, whereas Mn-Cr is characterized by an antiferromagnetic exchange that induces a ferrimagnetic spin arrangement along the chain. Detailed analyses of both static and dynamic magnetic properties have demonstrated without ambiguity the single-chain magnet (SCM) behavior of these three systems, whereas Mn-Co is merely paramagnetic with S(Mn)=2 and D/k(B)=-5.3?K (D being a zero-field splitting parameter). At low temperatures, the Mn-M compounds with M=Fe, Mn, and Cr display remarkably large M versus H hysteresis loops for applied magnetic fields along the easy magnetic direction that corresponds to the chain direction. The temperature dependence of the associated relaxation time for this series of compounds systematically exhibits a crossover between two Arrhenius laws corresponding to infinite-chain and finite-chain regimes for the SCM behavior. These isostructural hetero-spin SCMs offer a unique series of alternating [-Mn-NC-M-CN-] chains, enabling physicists to test theoretical SCM models between the Ising and Heisenberg limits. 相似文献
14.
《Journal of Coordination Chemistry》2012,65(22):3914-3922
Two octacyanometallate-based NiII–MIV [M?=?Mo(1), W(2)] bimetallic assemblies chelated with tetradentate macrocyclic ligands have been synthesized by slow diffusion and characterized structurally. In both complexes, M and Ni centers acting as linker and connector, respectively, are connected by M–CN–Ni–NC–M linkages to form a 3-D diamond-type topological network. Magnetic behaviors of both complexes show a very weak antiferromagnetic interaction between NiII ions mediated by the diamagnetic [M(CN)8]4? bridges. 相似文献
15.
Ferrando-Soria J Pardo E Ruiz-García R Cano J Lloret F Julve M Journaux Y Pasán J Ruiz-Pérez C 《Chemistry (Weinheim an der Bergstrasse, Germany)》2011,17(7):2176-2188
A series of neutral oxamato‐bridged heterobimetallic chains of general formula [MCu(Lx)2(S)2] ? p S ? q H2O [p=0–1, q=0–2.5; L1=N‐2,6‐dimethylphenyloxamate, S=DMF with M=Mn ( 1 a ) and Co ( 1 b ); L2=N‐2,6‐diethylphenyloxamate, S=DMF with M=Mn ( 2 a ) and Co ( 2 b ) or S=DMSO with M=Mn ( 2 c ) and Co ( 2 d ); L3=N‐2,6‐diisopropylphenyloxamate, S=DMF with M=Mn ( 3 a ) and Co ( 3 b ) or S=DMSO with M=Mn ( 3 c ) and Co ( 3 d )] were prepared by treating the corresponding anionic oxamatocopper(II) complexes [Cu(Lx)2]2? (x=1–3) with M2+ cations (M=Mn and Co) in DMF or DMSO as the solvent. The single‐crystal X‐ray structures of 2 a and 3 a reveal the occurrence of well‐isolated, zigzag, oxamato‐bridged manganese(II)–copper(II) chains. The intrachain Cu ??? Mn distances across the oxamato bridge are 5.3761(7) and 5.4002(17) Å for 2 a and 3 a , respectively, whereas the shortest interchain Mn ??? Mn distances are 9.4475(16) and 8.1649(14) Å for 2 a and 3 a , respectively. All of these MIICuII chains (M=Mn and Co) exhibit 1D ferrimagnetic behaviour with moderately strong intrachain antiferromagnetic coupling between the square‐planar CuII and octahedral high‐spin MII ions across the oxamato bridge [?J=31.4–35.2 and 33.4–44.8 cm?1, respectively; H =∑i?J S M,i( S Cu,i+ S Cu,i?1)]. Only the CoIICuII chains show slow magnetic relaxation effects characteristic of single‐chain magnets (SCMs). Analysis of the magnetic relaxation dynamics of 3 d shows a thermally activated mechanism (Arrhenius law dependence) with values of the pre‐exponential factor (τ0=2.6×10?9 s) and activation energy (Ea=7.7 cm?1) that are typical of SCMs. In contrast, two relaxation regimes are observed for 2 d in different temperature regions (τ0=3.2×10?10 s and Ea=24.7 cm?1 for T<4.5 K and τ0=3.2×10?14 s and Ea=37.5 cm?1 for T>4.5 K). 相似文献
16.
Atanasov M Comba P Förster S Linti G Malcherek T Miletich R Prikhod'ko AI Wadepohl H 《Inorganic chemistry》2006,45(19):7722-7735
The reaction of [M(CN)6]3- (M = Cr3+, Fe3+, Co3+) with the nickel(II) complex of 2,4-diamino-1,3,5-triazin-6-yl-{3-(1,3,5,8,12-pentaazacyclotetradecane)} ([NiL]2+) in excess of ANO3 or ACl (A = Li+, Na+, K+, Rb+, Cs+, NH4+) leads to the cyano-bridged dinuclear assemblies A{[NiL][M(CN)6]}.xH2O (x = 2-5). X-ray structures of Li{[NiL][Cr(CN)6]}.5H2O, NH4{[NiL][Cr(CN)6]}.3.5H2O, K{[NiL][Cr(CN)6]}.4H2O, K{[NiL][Fe(CN)6]}.4H2O, Rb{[NiL][Fe(CN)6]}.3.5H2O, and Cs{[NiL][Fe(CN)6]}.3.5H2O, as well as the powder diffractometry of the entire Fe(III) series, are reported. The magnetic properties of the assemblies are dependent on the monocation A and discussed in detail. New efficient pathways for ferromagnetic exchange between Ni(II) and Fe(III) or Cr(III) are demonstrated. Field dependencies of the magnetization for the Fe(III) samples at low temperature and low magnetic field indicate a weak interchain antiferromagnetic coupling, which is switched to ferromagnetic coupling at increasing magnetic field (metamagnetic behavior). The interchain magnetic coupling can be tuned by the size of the A cations. 相似文献
17.
Three bimetallic assemblies with alternate homometallic bridges through chloride ligands and heterometallic bridges through cyanide ligands of formula [(323)(2)Cu(2)(Cl)M(CN)(6)](n).2n(H(2)O), where 323 = N,N'-bis(3-aminopropyl)ethylenediamine and M = Co(3+) for 1, Fe(3+) for 2, and Cr(3+) for 3, were synthesized. They have been characterized structurally, analytically, spectroscopically, and magnetically. All three assemblies crystallize in the monoclinic system in the same space group P2(1)/n, with a = 11.642(2) A, b = 10.285(3) A, c = 13.622(2) A, beta = 95.69(3) degrees, V = 1623.1(6) A(3), and Z = 4 for 1; a = 11.681(4) A, b = 10.315(3) A, c = 13.567(5) A, beta = 95.62(3) degrees, V = 1626.8(9) A(3), Z = 4 for 2, and a = 11.782(4) A, b = 10.386(2) A, c = 13.755(4) A, beta = 95.51(3) degrees, V = 1657.4(8) A(3), Z = 4 for 3. Crystal structure analyses reveal that one-dimensional zigzag chains propagate in two different crystallographic directions (a and b) which are held together during the course of their propagation. All three assemblies have a homometallic Cu-Cl-Cu core in common. Assembly 1 exhibits metamagnetic behavior and shows weak antiferromagnetic interactions between Cu(2+) paramagnetic centers, through the chloride bridges. The Neel temperature, T(N), is 3.5 K, and the critical field is 4 T. In the presence of a magnetic field larger than 4 T, the local spin doublets of Cu(2+) in the assembly 1 remain in parallel arrangements. Assemblies 2 and 3 may be described as an alternative repetition of the antiferromagnetically coupled Cu-Cl-Cu fragment and ferromagnetically coupled Cu-CN-Fe(3+)/Cr(3+)fragment. The overall magnetic character of the strings in assemblies 2 and 3 are antiferromagnetic. Ferromagnetic interaction evidenced by the (Cu-CN-Fe(3+)/Cr(3+)) fragment was masked by the antiferromagnetic interaction between the Cu(2+) centers through the chloride bridge. The magnetic properties agree well with those expected for two [323 Cu(2+)] and a [Fe(CN)](3+) unit with spin-orbit coupling effect of the low-spin iron(III) ions for 2 and for two [323 Cu(2+)] and a [Cr(CN)](3+) unit for 3. In aqueous solution, trinuclear [(323)(2)Cu(2)M(CN)(6)](+) and dinuclear [(323)CuM(CN)(6)](-) species were observed. 相似文献
18.
On the basis of high-spin metal-cyanide clusters of Mn(III)(6)M(III) (M = Cr, Fe, Co), three one-dimensional (1D) chain complexes, [Mn(salen)](6)[Cr(CN)(6)](2)·6CH(3)OH·H(2)O (1), [Mn(5-CH(3))salen)](6)[Fe(CN)(6)](2)·2CH(3)CN·10H(2)O (2), and [Mn(5-CH(3))salen)](6)[Co(CN)(6)](2)·2CH(3)CN·10H(2)O (3) [salen = N,N'-ethylenebis(salicylideneiminato) dianion], have been synthesized and characterized structurally as well as magnetically. Complexes 2 and 3 are isomorphic but slightly different from complex 1. All three complexes contain a 1D chain structure which is comprised of alternating high-spin metal-cyanide clusters of [Mn(6)M](3+) and a bridging group [M(CN)(6)](3-) in the trans mode. Furthermore, the three complexes all exhibit extended 3D supramolecular networks originating from short intermolecular contacts. Magnetic investigation indicates that the coupling mechanisms are intrachain antiferromagnetic interactions for 1 and ferromagnetic interactions for 2, respectively. Complex 3 is a magnetic dilute system due to the diamagnetic nature of Co(III). Further magnetic investigations show that complexes 1 and 2 are dominated by the 3D antiferromagnetic ordering with T(N) = 7.2 K for 1 and 9.5 K for 2. It is worth noting that the weak frequency-dependent phenomenon of AC susceptibilities was observed in the low-temperature region in both 1 and 2, suggesting the presence of slow magnetic relaxations. 相似文献
19.
Kuppuswamy S Cooper BG Bezpalko MW Foxman BM Powers TM Thomas CM 《Inorganic chemistry》2012,51(3):1866-1873
The heterobimetallic complexes [Mn((i)PrNPPh(2))(3)Cu((i)PrNHPPh(2))] (1) and [Fe((i)PrNPPh(2))(3)Cu((i)PrNHPPh(2))] (2) have been synthesized by the one pot reaction of LiN(i)PrPPh(2), MCl(2) (M = Mn, Fe), and CuI in high yield. Addition of excess CuI into 2 or directly to the reaction mixture led to the formation of a heterotrimetallic [Fe((i)PrNPPh(2))(3)Cu(2)((i)PrNPPh(2))] (3) in good yield. Complexes 1-3 have been characterized by means of elemental analysis, paramagnetic (1)H NMR, UV-vis spectroscopy, cyclic voltammetry, and single crystal X-ray analysis. In all three complexes, Mn or Fe are in the +2 oxidation state and have a high spin electron configuration, as evidenced by solution Evans' method. In addition, the oxidation state of Fe in complex 3 is confirmed by zero-field (57)Fe M?ssbauer spectroscopy. X-ray crystallography reveals that the three coordinate Mn/Fe centers in the zwitterionic complexes 1-3 adopt an unusual trigonal planar geometry. 相似文献
20.
Zhao XQ Cui P Zhao B Shi W Cheng P 《Dalton transactions (Cambridge, England : 2003)》2011,40(4):805-819
The structures, luminescent and magnetic properties of three series of coordination polymers with formulas-{[Fe(3)Ln(2)(L(1))(6)(H(2)O)(6)]·xH(2)O}(n) (Ln = Pr-Er; 1-9), {[Co(3)Ln(2)(L(1))(6)(H(2)O)(6)]·yH(2)O}(n) (Ln = Pr-Dy, Yb; 10-17) and {[Co(2)Ln(L(2))(HL(2))(2)(H(2)O)(7)]·zH(2)O}(n) (Ln = Eu-Yb; 18-25) (H(2)L(1) = pyridine-2,6-dicarboxylic acid, H(3)L(2) = 4-hydroxyl-pyridine-2,6-dicarboxylic acid) were systematically explored in this contribution. [Fe(II)(HS)-L(1)-Ln(III)] (1-9) and [Co(II)-L(1)-Ln(III)] (10-17) series are isostructural, and display 3D porous networks with 1D nanosized channels constructed by Fe/Co-OCO-Ln linkages. Furthermore, two types of "water" pipes are observed in 1D channels. [Co(II)-L(2)-Ln(III)] (18-25) series exhibit 2D open frameworks based on double-stranded helical motifs, which are further assembled into 3D porous structures by intermolecular hydrogen bonds between hydroxyl groups. The variety of the resulting structures is mainly due to the HO-substitution effect. These 3D coordination polymers show considerably high thermal stability, and do not decomposed until 400 °C. The high-spin Fe(II) ion in [Fe(II)(HS)-L(1)-Ln(III)] was confirmed by X-ray photoelectron spectroscopy, M?ssbauer spectroscopy and magnetic studies. The luminescent spectra of coordination polymers associated with Sm(III), Eu(III), Tb(III) and Dy(III) were systematically investigated, and indicate that different d-metal ions in d-f systems may result in dissimilar luminescent properties. The magnetic properties of [Fe(II)(HS)-L(1)-Ln(III)] (3, 6, 7, 9, 13), [Co(II)-L(1)-Ln(III)] (15-17) and [Co(II)-L(2)-Ln(III)] (19-24) coordination polymers were also studied, and the χ(M)T values decrease with cooling. For the single ion behavior of Co(II) and Ln(III) ions, the magnetic coupling nature between Fe(II)(HS)/Co(II) and Ln(III) ions cannot be clearly depicted as antiferromagnetic coupling. 相似文献