Copper(II) complexes of bis(1,4,7-triazacyclononane) ligands with polymethylene bridging groups: An equilibrium and structural study

被引:49
作者
Haidar, R [1 ]
Ipek, M [1 ]
DasGupta, B [1 ]
Yousaf, M [1 ]
Zompa, LJ [1 ]
机构
[1] UNIV MASSACHUSETTS,DEPT CHEM,BOSTON,MA 02125
关键词
D O I
10.1021/ic970070f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Copper(II) complexation by a series of Ligands containing two 1,4,7-triazacyclononane, [9]aneN(3), groups conjoined by polymethylene chains two to six carbons in length is described. Equilibrium modeling studies in aqueous solution using pH-potentiometry indicate that the smallest homologue of the series, EM2, forms only Cu(EM2)(2+) in dilute aqueous solutions. All other ligands of the series form stable 1:1 (protonated and nonprotonated) and 2:1 dicopper(II) (hydroxo and non-hydroxo) complexes. Those ligands that contain bridging chains of four or more carbon atoms likely form dimeric or oligomeric complex species in solution. The EM ligands with the shortest polymethylene bridging groups form the most stable 1:1 species. There is little difference among the ligands (n = 3-6) in complex stability of the protonated, CuH2(EMn)(4+), and dicopper(II), Cu-2(EMn)(4+), species. W-vis spectroscopic continuous variation studies at pH 4.0 and 7.5 are interpreted on the basis of the principal equilibrium species obtained from the equilibrium models. Single-crystal X-ray diffraction studies on four complexes ([Cu(EM2)]SO4 . 6H(2)O (1), [Cu-2(EM2)Cl-4]. 2H(2)O (2), [Cu-2(EM6)Cl-4] (3), and [Cu(EM3)][ZnBr4]. H2O (4)) characterize structural features of several 1:1 monomeric and dicopper(II) complexes in the crystalline solid. The monomeric compounds contain CuN6 chromophores while the dicopper(IT) compounds contain square pyramidal CuN3Cl2 coordination geometry. Compound 1 crystallizes in space group <P(1)over bar> with a = 7.849(2) Angstrom, b = 9.783(2) Angstrom, c = 16.919(5) Angstrom, alpha = 78.42(3)degrees, beta = 85.76(3)degrees, gamma = 73.06(3)degrees, and Z = 2. 2: P2(1)/n with a = 9.689(3) Angstrom, b = 11.733(3) Angstrom, c = 10.124(3) Angstrom, beta = 98.20(2)degrees, and Z = 2. 3: P2(1)/n with a = 7.278(2) Angstrom, b = 12.416(3) Angstrom, c = 13.781(2) Angstrom, beta = 90.15(2)degrees, and Z = 2. 4: P2(1)/c with a = 9.295(3) Angstrom, b = 16.233(4) Angstrom, c = 16.544(5) Angstrom, beta = 92.62(2)degrees, and Z = 4. Cyclic voltammograms of aqueous solutions prepared by dissolving [Cu-2(EM2)Cl-4]. 2H(2)O confirm its dissociation to Cu(EM2)(2+). Aqueous solutions containing 1:1 molar ratios of Cu(II) and EM2 in 0.1 mol dm(-3) KCl at 25 degrees C show a one-electron chemically reversible reduction at scan rates of 500 mV s(-1) with E-1/2 (Cu(II)-Cu(I)) = -868 mV relative to SCE. EPR (X- and Q- band) spectra of frozen solutions (1:1 DMSO/H2O and glycerol/H2O) of Cu(EM2)(2+) at 100 K are typical of axial copper(II) features (X-band parameters: g(parallel to) = 2.225 (A(parallel to) = 164 x 10(-4)) and g(perpendicular to) = 2.045).
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页码:3125 / 3132
页数:8
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共 39 条
[1]   METAL-COMPLEXES WITH MACROCYCLIC LIGANDS .39. MONONUCLEAR AND BINUCLEAR COPPER(II) COMPLEXES OF A BRIDGING BIS[1,4,7-TRIAZACYCLONONANE] [J].
BEHLE, L ;
NEUBURGER, M ;
ZEHNDER, M ;
KADEN, TA .
HELVETICA CHIMICA ACTA, 1995, 78 (03) :693-702
[2]   PREPARATION AND CRYSTAL AND MOLECULAR-STRUCTURE OF DIBROMO(1,4,7-TRIAZACYCLONONANE)COPPER(II) [J].
BEREMAN, RD ;
CHURCHILL, MR ;
SCHABER, PM ;
WINKLER, ME .
INORGANIC CHEMISTRY, 1979, 18 (11) :3122-3125
[3]   STUDIES ON TRANSITION-METAL MACROCYCLIC COMPLEXES - SINGLE-CRYSTAL X-RAY STRUCTURE AND ELECTROCHEMISTRY OF THE BIS-MACROCYCLIC COMPLEX [CU(1,4,7-TRIAZACYCLONONANE)2][CIO4]2.2H2O(1,4,7-TRIAZACYCLONONANE) [J].
BEVERIDGE, AD ;
LAVERY, AJ ;
WALKINSHAW, MD ;
SCHRODER, M .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1987, (02) :373-377
[4]   SYNTHESIS OF A NEW BINUCLEATING LIGAND LH(4) - SYNTHESIS AND X-RAY STRUCTURES OF ANTI-[CO-2(LH(4))(OH2)(2)](NO3)(4).5H2O, ANTI-[NI-2(LH(4))(NCME)(2)](PF6)(4).4H2O, ANTI-[ZN-2(LH(4))(NO3)(2)](NO3)(2) AND SYN-[CU-2(LH(2))](BPH(4))(2) [J].
BLAKE, AJ ;
DONLEVY, TM ;
ENGLAND, PA ;
FALLIS, IA ;
PARSONS, S ;
ROSS, SA ;
SCHRODER, M .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (17) :1981-1982
[5]   Binuclear copper(II) complexes of bis(pentadentate) ligands derived from alkyl-bridged bis(1,4,7-triazacyclonane) macrocycles [J].
Brudenell, SJ ;
Spiccia, L ;
Tiekink, ERT .
INORGANIC CHEMISTRY, 1996, 35 (07) :1974-1979
[6]   COMPARTMENTAL LIGANDS - ROUTES TO HOMO-DINUCLEAR AND HETERO-DINUCLEAR COMPLEXES [J].
CASELLATO, U ;
VIGATO, PA .
CHEMICAL SOCIETY REVIEWS, 1979, 8 (02) :199-220
[7]   SYNTHESES AND REACTIVITY OF NICKEL-COMPLEXES OF 8-AZA-1,5-DITHIACYCLODECANE AND THE MACROBICYCLIC LIGAND 1,2-BIS(8-AZA-1,5-DITHIA-8-CYCLODECANYL)ETHANE [J].
CHANDRASEKHAR, S ;
MCAULEY, A .
INORGANIC CHEMISTRY, 1992, 31 (11) :2234-2240
[8]   ELECTROCATALYTIC PROPERTIES OF NI(CYCLAM)2+ AND NI2(BISCYCLAM)4+ WITH RESPECT TO CO2 AND H2O REDUCTION [J].
COLLIN, JP ;
JOUAITI, A ;
SAUVAGE, JP .
INORGANIC CHEMISTRY, 1988, 27 (11) :1986-1990
[9]   INDIRECT COOPERATIVE EFFECTS LEADING TO SYNERGISM IN BIMETALLIC HOMOGENEOUS CATALYSTS CONTAINING AZOLATES AS BRIDGING LIGANDS [J].
ESTERUELAS, MA ;
GARCIA, MP ;
LOPEZ, AM ;
ORO, LA .
ORGANOMETALLICS, 1991, 10 (01) :127-133
[10]   SUPERQUAD - AN IMPROVED GENERAL PROGRAM FOR COMPUTATION OF FORMATION-CONSTANTS FROM POTENTIOMETRIC DATA [J].
GANS, P ;
SABATINI, A ;
VACCA, A .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1985, (06) :1195-1200