RESUMO
Mononuclear rare-earth metal alkyl complexes supported by tetradentate dianionic bis(amino-oxazoline) ligands have been synthesized, and their reactivity toward small molecules and catalytic performance on ring-opening polymerization have been studied. Treatment of Ln(CH2SiMe3)3(THF)2 (Ln = Sc, Y; THF = tetrahydrofuran) with the bis(amino-oxazoline) proligand H2L afforded the corresponding rare-earth metal monoalkyl complexes L-Ln(CH2SiMe3)(THF)x (Ln = Sc, x = 0 (1); Ln = Y, x = 1 (2)). The isopropyl-substituted Sc alkyl complex L'-Sc(CH2SiMe3) (3) and the analogue Y silylamide complex L-Y[N(SiHMe2)2] (4) have been prepared by a similar method. Complexes 1 and 2 were stable in solution at room temperature but transformed gradually at elevated temperature to give a nucleophilic addition product for Sc (5) and an oxazoline ring-opened dimeric complex for Y (6). Reactions of 1 with elemental sulfur and selenium each led to insertion of one chalcogen into the Sc-C bond, and the corresponding six-coordinate mononuclear chalcogenolate complexes L-Sc(ECH2SiMe3)(THF) (E = S (7), Se (8)) were isolated. Treatment of 1 with an equimolar amount of aniline yielded the Sc anilide complex L-Sc(NHC6H5) (9), whereas the reaction of 1 with [NHEt3][BPh4] afforded the Sc ion-pair [L-Sc][BPh4] (10), which upon recrystallization led to formation of a THF-solvated product [L-Sc(THF)][BPh4] (11). Single-crystal X-ray diffraction analyses of complexes 1-3, 7-9, and 11 revealed the flexible coordination capability of the tetradentate bis(amino-oxazoline) ligand of upholding a mononuclear metal center via a torsion of the diaminobiphenyl axis. Complexes 1-4 were active catalysts for initiating the ring-opening polymerization of rac-lactide with good activity (TOF up to 3204 h-1) and heteroselectivity (Pr = 0.65-0.71). This study highlights the applicability of the well-defined tetradentate bis(amino-oxazoline) ligands for mononuclear rare-earth metal complexation and shed light on the new potential of rare-earth metal catalysts bearing this type of easily derivatizable polydentate ligand.
RESUMO
Tetravalent cerium alkoxide complexes supported by the Kläui tripodal ligand [Co(η5-C5H5){P(O)(OEt)2}3]- (LOEt-) have been synthesized, and their nucleophilic and redox reactivity have been studied. Treatment of the Ce(IV) oxo complex [CeIV(LOEt)2(O)(H2O)]·MeCONH2 (1) with iPrOH or reaction of [CeIV(LOEt)2Cl2] (2) with Ag2O in iPrOH afforded the Ce(IV) dialkoxide complex [CeIV(LOEt)2(OiPr)2] (3-iPr). The methoxide and ethoxide analogues [CeIV(LOEt)2(OR)2] (R = Me (3-Me), Et (3-Et)) have been prepared similarly from 2 and Ag2O in ROH. Reaction of 3-iPr with an equimolar amount of 2 yielded a new Ce(IV) complex that was formulated as the chloro-alkoxide complex [CeIV(LOEt)2(OiPr)Cl] (4). Treatment of 3-iPr with HX and methyl triflate (MeOTf) afforded [Ce(LOEt)2X2] (X- = Cl-, NO3-, PhO-) and [CeIV(LOEt)2(OTf)2], respectively, whereas treatment with excess CO2 in hexane led to isolation of the Ce(IV) carbonate [CeIV(LOEt)2(CO3)]. 3-iPr reacted with water in hexane to give a Ce(III) complex and a Ce(IV) species, presumably the reported tetranuclear oxo cluster [CeIV4(LOEt)4(O)5(OH)2]. The Ce(IV) alkoxide complexes are capable of oxidizing substituted phenols, possibly via a proton-coupled electron transfer pathway. Treatment of 3-iPr with ArOH afforded the Ce(III) aryloxide complexes [CeIII(LOEt)2(OAr)] (Ar = 2,4,6-tri-tert-butylphenyl (5), 2,6-diphenylphenyl (6)). On the other hand, a Ce(III) complex containing a monodeprotonated 2,2'-biphenol ligand, [CeIII(LOEt)2(tBu4C12H4O2H)] (7) (tBu4C12H4O2H2 = 4,4',6,6'-tetra-tert-butyl-2,2'-biphenol), was isolated from the reaction of 3-iPr with 2,4-di-tert-butylphenol. The crystal structures of complexes 3-iPr, 3-Me, 3-Et, and 5-7 have been determined.
RESUMO
A combined experimental and theoretical investigation on the cerium(IV) oxo complex [(LOEt )2 Ce(=O)(H2 O)]â MeC(O)NH2 (1; LOEt - =[Co(η5 -C5 H5 ){P(O)(OEt)2 }3 ]- ) demonstrates that the intermediate spin-state nature of the ground state of the cerium complex is responsible for the versatility of its reactivity towards small molecules such as CO, CO2 , SO2 , and NO. CASSCF calculations together with magnetic susceptibility measurements indicate that the ground state of the cerium complex is of multiconfigurational character and comprised of 74 % of CeIV and 26 % of CeIII . The latter is found to be responsible for its reductive addition behavior towards CO, SO2 , and NO. This is the first report to date on the influence of the multiconfigurational ground state on the reactivity of a metal-oxo complex.
RESUMO
Dinuclear iron nitrido phthalocyanine complexes are of interest owing to their applications in catalytic oxidation of hydrocarbons. While nitrido-bridged diiron phthalocyanine complexes are well documented, the oxidation chemistry of heterodinuclear iron(IV) phthalocyanine nitrides has not been well explored. In this paper we report on the synthesis of a heterometallic FeIV/RuIV phthalocyanine nitride and its oxidation to yield phthalocyanine cation radical and hydroxyphthalocyanine complexes. Treatment of [FeII(Pc)] (Pc2- = phthalocyanine dianion) with [RuVI(LOEt)(N)Cl2] (LOEt- = [Co(η5-C5H5){P(O)(OEt)2}3]-) (1) afforded the heterometallic µ-nitrido complex [Cl2(LOEt)RuIV(µ-N)FeIV(Pc)(H2O)] (2) that contains an RuIV=N = FeIV linkage with the Ru-N and Fe-N distances of 1.689(6) and 1.677(6) Å, respectively, and Ru-N-Fe angle of 176.0(4)°. Substitution of 2 with 4- tert-butylpyridine (Bupy) gave [Cl2(LOEt)RuIV(µ-N)FeIV(Pc)(Bupy)]. The cyclic voltammogram of 2 displayed a reversible Pc-centered oxidation couple at +0.18 V versus Fc+/0 (Fc = ferrocene). The oxidation of 2 with [N(4-BrC6H4)3]SbCl6 led to isolation of the cationic complex [Cl2(LOEt)RuIV(µ-N)FeIV(Pc·+)(H2O)][SbCl6]0.85[SbCl5(OH)]0.15 (2[SbCl6]0.85[SbCl5(OH)]0.15), whereas that with PhICl2 yielded the chloride complex [Cl2(LOEt)RuIV(µ-N)FeIV(Pc·+)Cl] (3). Complexes 2[SbCl6]0.85[SbCl5(OH)]0.15 and 3 have been characterized by X-ray crystallography. The UV/visible spectra of 2+ (λmax = 515 and 747 nm) and 3 (λmax = 506 and 748 nm) displayed absorption bands that are characteristic of Pc cation radical. The EPR spectrum of 3 showed a signal with the g value of 2.0012 (width = 5 G) that is consistent with an organic radical. The spectroscopic data support the formulation of 2+ and 3 as RuIV-FeIV Pc cation radical complexes. The reaction of 2 with PhI(CF3CO2)2 in dried CH2Cl2 afforded a mixture of [Cl2(LOEt)RuIV(µ-N)FeIV(Pc·+)(CF3CO2)] (4) and a hydroxyphthalocyanine complex, [Cl2(LOEt)RuIV(µ-N)FeIV(Pc-OH)(H2O)](CF3CO2) (5), whereas that in wet CH2Cl2 (containing ca. 0.5% water) led to isolation of 5 as the sole product. Complex 4 was independently prepared by salt metathesis of 3 with AgCF3CO2.
RESUMO
Heterobimetallic nitrido porphyrin complexes with the [(L)(por)M-N-M'(LOEt)Cl2] formula {por2- = 5,10,15,20-tetraphenylporphyrin (TPP2-) or 5,10,15,20-tetra(p-tolyl)porphyrin (TTP2-) dianion; LOEt- = [Co(η5-C5H5){P(O)(OEt)2}3]-; M = Fe, Ru, or Os; M' = Ru or Os; L = H2O or pyridine} have been synthesized, and their electrochemistry has been studied. Treatment of trans-[Fe(TPP)(py)2] (py = pyridine) with Ru(VI) nitride [Ru(LOEt)(N)Cl2] (1) afforded Fe/Ru µ-nitrido complex [(py)(TPP)Fe(µ-N)Ru(LOEt)Cl2] (2). Similarly, Fe/Os analogue [(py)(TPP)Fe(µ-N)Os(LOEt)Cl2] (3) was obtained from trans-[Fe(TPP)(py)2] and [Os(LOEt)(N)Cl2]. However, no reaction was found between trans-[Fe(TPP)(py)2] and [Re(LOEt)(N)Cl(PPh3)]. Treatment of trans-[M(TPP)(CO)(EtOH)] with 1 afforded µ-nitrido complexes [(H2O)(TPP)M(µ-N)Ru(LOEt)Cl2] [M = Ru (4a) or Os (5)]. TTP analogue [(H2O)(TTP)Ru(µ-N)Ru(LOEt)Cl2] (4b) was prepared similarly from trans-[Ru(TTP)(CO)(EtOH)] and 1. Reaction of [(H2O)(por)M(µ-N)M(LOEt)Cl2] with pyridine gave adducts [(py)(por)M(µ-N)Ru(LOEt)Cl2] [por = TTP, and M = Ru (6); por = TPP, and M = Os (7)]. The diamagnetism and short (por)M-N(nitride) distances in 2 [Fe-N, 1.683(3) Å] and 4b [Ru-N, 1.743(3) Å] are indicative of the MIVâNâM'IV bonding description. The cyclic voltammograms of the Fe/Ru (2) and Ru/Ru (4b) complexes in CH2Cl2 displayed oxidation couples at approximately +0.29 and +0.35 V versus Fc+/0 (Fc = ferrocene) that are tentatively ascribed to the oxidation of the {LOEtRu} and {Ru(TTP)} moieties, respectively, whereas the Fe/Os (3) and Os/Ru (5) complexes exhibited Os-centered oxidation at approximately -0.06 and +0.05 V versus Fc+/0, respectively. The crystal structures of 2 and 4b have been determined.
RESUMO
The reactivity of the cerium(IV) oxo complex [(LOEt)2CeIV(âO)(H2O)]·MeC(O)NH2 (1; LOEt- = [CoCp{P(O)(OEt)2}3]-, where Cp = η5-C5H5) toward electrophiles and Brønsted acids has been investigated. The treatment of 1 with acetic anhydride afforded the diacetate complex [CeIV(LOEt)2(O2CMe)2] (2). The reaction of 1 with B(C6F5)3 yielded [CeIV(LOEt)2(Me2CONH2)2][B(C6F5)3(OH)]2 (3), in which the [B(C6F5)3(OH)]- anions are H-bonded to the O-bound acetamide ligands. The treatment of 1 with HCl and HNO3 afforded [CeIV(LOEt)2Cl2] and [CeIV(LOEt)2(NO3)2], respectively. Protonation of 1 with triflic acid (HOTf) gave the diaqua complex [CeIV(LOEt)2(H2O)2](OTf)2 (4), in which the triflate anions are H-bonded to the two aqua ligands. The treatment of 1 with phenol afforded the phenoxide complex [CeIV(LOEt)2(OPh)2] (5). The oxo-bridged bimetallic complex [(LOEt)2(Me2CONH2)CeIV(O)NaLOEt] (6) with the Ce-Ooxo and Na-Ooxo distances of 1.953(4) and 2.341(4) Å, respectively, was obtained from the reaction of 1 with [NaLOEt]. Density functional theory calculations showed that the model complex [(LOMe)2CeIV(Me2CONH2)(O)NaLOMe] (6A; LOMe- = [CoCp{P(O)(OMe)2}3]-) contains a polarized CeâO multiple bond. The energy for dissociation of the {NaLOMe} fragment from 6A in acetonitrile was calculated to be +33.7 kcal/mol, which is higher than that for dissociation of the H-bonded acetamide from [(LOMe)2CeIV(âO)(H2O)]·MeC(O)NH2 (1A) (calculated to be +17.4 kcal/mol). In hexanes containing trace water, complex 1 decomposed readily to a mixture of a tetranuclear cerium(IV) oxo cluster, [CeIV4(LOEt)4(µ4-O)(µ2-O)4(µ2-OH)2] (7), and a cerium(III) complex, [CeIII(LOEt)2(H2O)2][LOEt] [8(LOEt)], whereas the cerium/sodium oxo complex 6 is stable under the same conditions. The crystal structures of 3, 4·H2O, 6, and 8(LOEt) have been determined.
RESUMO
A tetranuclear Ce(IV) oxo cluster compound containing the Kläui tripodal ligand [Co(η(5) -C5 H5 ){P(O)(OEt)2 }3 ](-) (LOEt (-) ) has been synthesized and its reactions with H2 O2 , CO2 , NO, and Brønsted acids have been studied. The treatment of [Ce(LOEt )(NO3 )3 ] with Et4 NOH in acetonitrile afforded the tetranuclear Ce(IV) oxo cluster [Ce4 (LOEt )4 O7 H2 ] (1) containing an adamantane-like {Ce4 (µ2 -O)6 } core with a µ4 -oxo ligand at the center. The reaction of 1 with H2 O2 resulted in the formation of the peroxo cluster [Ce4 (LOEt )4 (µ4 -O)(µ2 -O2 )4 (µ2 -OH)2 ] (2). The treatment of 1 with CO2 and NO led to isolation of [Ce(LOEt )2 (CO3 )] and [Ce(LOEt )(NO3 )3 ], respectively. The protonation of 1 with HCl, ROH (R=2,4,6-trichlorophenyl), and Ph3 SiOH yielded [Ce(LOEt )Cl3 ] (3), [Ce(LOEt )(OR)3 ] (4), and [Ce(LOEt )(OSiPh3 )3 ] (5), respectively. The chloride ligands in 3 are labile and can be abstracted by silver(I) salts. The treatment of 3 with AgOTs (OTs(-) =tosylate) and Ag2 O afforded [Ce(LOEt )(OTs)3 ] (6) and 1, respectively. The electrochemistry of the Ce-LOEt complexes has been studied by using cyclic voltammetry. The crystal structures of complexes 1-5 have been determined.
RESUMO
Whereas terminal oxo complexes of transition and actinide elements are well documented, analogous lanthanide complexes have not been reported to date. Herein, we report the synthesis and structure of a cerium(IV) oxo complex, [CeO(LOEt )2 (H2 O)]â MeC(O)NH2 (1; LOEt (-) =[Co(η(5) -C5 H5 ){P(O)(OEt)2 }3 ](-) ), featuring a short CeO bond (1.857(3)â Å). DFT calculations indicate that the hydrogen bond to cocrystallized acetamide plays a key role in stabilizing the CeO moiety of 1 in the solid state. Complex 1 exhibits oxidizing and nucleophilic reactivity.
Assuntos
Cério/química , Complexos de Coordenação/química , Acetamidas/química , Cristalografia por Raios X , Ligação de Hidrogênio , Conformação Molecular , Oxigênio/química , Teoria QuânticaRESUMO
η(5)-η(1) ring slippage of [OsCp2] (Cp = η(5)-C5H5) and [Ru(η(5)-ind)2] (ind = indenyl) resulting from reaction with the ruthenium(VI) nitride [Ru(L(OEt))(N)Cl2] (1; L(OEt)(-) = [CoCp{P(O)(OEt)2}3](-)) is reported. The treatment of [OsCp2] or [Ru(η(5)-ind)2] with 1 resulted in η(5)-η(1) ring slippage of the cycloolefin ligands and formation of the trinuclear nitrido complexes [Cp(η(1)-C5H5)Os(NRuL(OEt)Cl2)2] (2) or [(η(5)-ind)(η(1)-ind)Ru(NRuL(OEt)Cl2)2] (3). No reactions were found between [OsCp2] and amines, such as pyridine and 2,2'-bipyridyl, or other metal nitrides, such as [Os(L(OEt))(N)Cl2], indicating that the electrophilic property of 1 is essential for ring slippage. The crystal structures of 2 and 3 have been determined. The short Os-N distances in 2 [1.833(5) and 1.817(5) Å] and the (ind)Ru-N distances in 3 [1.827(5) and 1.852(5) Å] are indicative of multiple bond character, consistent with density functional theory (DFT) calculations. Therefore, 2 and 3 may be described by two resonance forms: Ru(VI)-M(II)-Ru(VI) and Ru(IV)-M(VI)-Ru(IV) (M = Os, Ru). Also, DFT calculations indicate that for the reaction of 1 with [OsCp2] or [Ru(η(5)-ind)2], η(5)-η(1) ring slippage is energetically more favorable than the η(5)-η(3) counterpart. The driving force for η(5)-η(1) ring slippage is believed to be the formation of the strong M-N (M = Os, Ru) (multiple) bonds. By contrast, the same reaction with acetonitrile is energetically uphill, and thus no ring slippage occurs.
RESUMO
Heterometallic cerium(IV) perrhenate, permanganate, and molybdate complexes containing the imidodiphosphinate ligand [N(i-Pr2PO)2](-) have been synthesized, and their reactivity was investigated. Treatment of Ce[N(i-Pr2PO)2]3Cl (1) with AgMO4 (M = Re, Mn) afforded Ce[N(i-Pr2PO)2]3(ReO4) (2) or Ce2[N(i-Pr2PO)2]6(MnO4)2 (3). In the solid state, 3 is composed of a [Ce2{N(i-Pr2PO)2}6(MnO4)](+) moiety featuring a weak Ce-OMn interaction [Ce-OMn distance = 2.528(8) Å] and a noncoordinating MnO4(-) counteranion. While 3 is stable in the solid state and acetonitrile solution, it decomposes readily in other organic solvents, such as CH2Cl2. 3 can oxidize ethylbenzene to acetophenone at room temperature. Treatment of 1 with AgBF4, followed by reaction with [n-Bu4N]2[MoO4], afforded [Ce{N(i-Pr2PO)2}3]2(µ-MoO4) (4). Reaction of trans-Ce[N(i-Pr2PO)2]2(NO3)2 (5), which was prepared from (NH4)2Ce(NO3)6 and K[N(i-Pr2PO)2], with 2 equiv of [n-Bu4N][Cp*MoO3] yielded trans-Ce[N(i-Pr2PO)2]2(Cp*MoO3)2 (6). 4 can catalyze the oxidation of methyl phenyl sulfide with tert-butyl hydroperoxide with high selectivity. The crystal structures of complexes 3-6 have been determined.
Assuntos
Cério/química , Compostos de Manganês/química , Molibdênio/química , Compostos Organometálicos/química , Óxidos/química , Ácidos Fosfínicos/química , Rênio/química , Imidas/química , Modelos Moleculares , Estrutura Molecular , Compostos Organometálicos/síntese químicaRESUMO
Dinuclear Ti(IV), Zr(IV), and Ce(IV) oxo and peroxo complexes containing the imidodiphosphinate ligand [N(i-Pr(2)PO)(2)](-) have been synthesized and structurally characterized. Treatment of Ti(O-i-Pr)(2)Cl(2) with KN(i-Pr(2)PO)(2) afforded the Ti(IV) di-µ-oxo complex [Ti{N(i-Pr(2)PO)(2)}(2)](2)(µ-O)(2) (1) that reacted with 35% H(2)O(2) to give the peroxo complex Ti[N(i-Pr(2)PO)(2)](2)(η(2)-O(2)) (2). Treatment of HN(i-Pr(2)PO)(2) with Zr(O-t-Bu)(4) and Ce(2)(O-i-Pr)(8)(i-PrOH)(2) afforded the di-µ-peroxo-bridged dimers [M{N(i-Pr(2)PO)(2)}(2)](2)(µ-O(2))(2) [M = Zr (3), Ce (4)]. 4 was also obtained from the reaction of Ce[N(i-Pr(2)PO)(2)](3) with 35% H(2)O(2). Treatment of (Et(4)N)(2)[CeCl(6)] with 3 equiv of KN(i-Pr(2)PO)(2) afforded Ce[N(i-Pr(2)PO)(2)](3)Cl (5). Reaction of (Et(4)N)(2)[CeCl(6)] with 2 equiv of KN(i-Pr(2)PO)(2) in acetonitrile, followed by treatment with Ag(2)O, afforded the µ-oxo-bridged complex [Ce{N(i-Pr(2)PO)(2)}Cl](2)[µ-N(i-Pr(2)PO)(2)](2)(µ-O) (6). 6 undergoes ligand redistribution in CH(2)Cl(2) in air to give 5. The solid-state structures of [K(2){N(i-Pr(2)PO)(2)}(2)(H(2)O)(8)](n) and complexes 1-6 have been determined.
RESUMO
Dinuclear ruthenium nitrido complexes supported by the Kläui's tripodal ligand [CpCo{P(O)(OEt)(2)}(3)](-) (L(OEt)(-)) have been synthesized starting from the ruthenium(VI) nitrido precursor [L(OEt)Ru(VI)(N)Cl(2)] (1). Heating a solution of 1 in CCl(4) at reflux, followed by recrystallization from hexane under nitrogen, afforded the mixed-valence ruthenium(V)-ruthenium(IV) µ-nitrido complex [L(OEt)Cl(2)Ru(V)(µ-N)Ru(IV)Cl(2)L(OEt)] (2). The cyclic voltammogram of 2 exhibited reversible couples at 0.19 and 1.13 V versus Cp(2)Fe(+/0), which are assigned as the Ru(V)-Ru(IV)/Ru(IV)-Ru(IV) and Ru(V)-Ru(V)/Ru(V)-Ru(IV) couples, respectively. Recrystallization of 2 from Et(2)O/heptane in air yielded the diamagnetic Ru(IV)-Ru(IV) complex [H(13)O(6)][{L(OEt)Ru(IV)Cl(2)}(2)(µ-N)] ([H(13)O(6)][2]), which underwent cation exchange with n-Bu(4)NOH to give [n-Bu(4)N][2]. X-ray diffraction revealed that the complex anions in [H(13)O(6)][2] and [n-Bu(4)N][2] contain linear, symmetric Ru-N-Ru bridges. Treatment of 1 with [(η(6)-p-cymene)Ru(II)Cl(2)](2) in benzene afforded the tetranuclear ruthenium(IV) complex [L(OEt)Cl(2)Ru(IV)(µ-N)Ru(IV)(H(2)O)Cl(2)](2) (3) containing symmetric Ru(IV)-N-Ru(IV) bridges. The reaction of 1 with [Ru(II)(H)(Cl)(CO)(PCy(3))(2)] (Cy = cyclohexyl) gave the ruthenium(VI)-ruthenium(II) nitrido complex [L(OEt)Cl(2)Ru(VI)(µ-N)Ru(II)(H)Cl(CO)(PCy(3))(2)] (4). The observed short Ru(II)-N bond distance [1.915(5) Å] and high C-O stretching frequency (1985 cm(-1)) in 4 are suggestive of π interaction between Ru(II) and the nitride.
RESUMO
Bismuth(III) compounds containing the Kläui's oxygen tripodal ligand [CpCo{P(O)(OEt)(2)}(3)](-) (L(OEt)(-)) have been synthesized, and their interactions with dichromate in aqueous media were studied. The treatment of Bi(5)O(OH)(9)(NO(3))(4) with NaL(OEt) in water afforded [L(OEt)Bi(NO(3))(2)](2) (1), whereas that of BiCl(3) with NaL(OEt) in CH(2)Cl(2) yielded L(OEt)BiCl(2) (2). Chloride abstraction of 2 with AgX afforded [L(OEt)BiX(2)](2) [X(-) = triflate (OTf(-)) (3), tosylate (OTs(-)) (4)]. In aqueous solutions at pH > 4, 4 underwent ligand redistribution to give the bis(tripod) complex [(L(OEt))(2)Bi(H(2)O)][OTs] (5). The treatment of 4 with Na(2)Cr(2)O(7) in acetone/water afforded the Bi(III)/Cr(VI) oxo cluster [(L(OEt))(4)Bi(4)(µ(3)-CrO(4))(2)(µ(3)-Cr(2)O(7))(2)] (6) containing a unique Bi(4)Cr(4)O(12) oxometallic core. Compound 6 oxidized benzyl alcohol to give ca. 6 equiv of benzaldehyde. The reaction between 2 and CrO(3) yielded [L(OEt)Bi(OCrO(2)Cl)](2)(µ-Cl)(2) (7). The crystal structures of complexes 4-7 have been determined.
Assuntos
Bismuto/química , Cromo/química , Compostos Organometálicos/síntese química , Oxigênio/química , Cristalografia por Raios X , Ligantes , Modelos Moleculares , Compostos Organometálicos/químicaRESUMO
The treatment of [Ru(L(OEt))(N)Cl(2)] (1; L(OEt)(-) = [Co(η(5)-C(5)H(5)){P(O)(OEt)(2)}(3)](-)) with Et(3)SiH affords [Ru(L(OEt))Cl(2)(NH(3))] (2), whereas that with [Ru(L(OEt))(H)(CO)(PPh(3))] (3) gives the dinuclear imido complex [(L(OEt))Cl(2)Ru(µ-NH)Ru(CO)(PPh(3))(L(OEt))] (4). The imido group in 4 binds to the two ruthenium atoms unsymmetrically with Ru-N distances of 1.818(6) and 1.952(6) Å. The reaction between 1 and 3 at 25 °C in a toluene solution is first order in both complexes with a second-order rate constant determined to be (7.2 ± 0.4) × 10(-5) M(-1) s(-1).
RESUMO
In an effort to synthesize cyclometalated iridium complexes containing a tridentate C^N^C ligand, transmetallation of [Hg(HC^N^C)Cl] (1) (H2C^N^C = 2,6-bis(4-tert-butylphenyl)pyridine) with various organoiridium starting materials has been studied. The treatment of 1 with [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene) in acetonitrile at room temperature afforded a hexanuclear Ir4Hg2 complex, [Cl(κ2C,N-HC^N^C)(cod)IrHgIr(cod)Cl2]2 (2), which features Ir-Hg-Ir and Ir-Cl-Ir bridges. Refluxing 2 with sodium acetate in tetrahydrofuran (thf) resulted in cyclometalation of the bidentate HC^N^C ligand and formation of trinuclear [(C^N^C)(cod)IrHgIr(cod)Cl2] (3). On the other hand, refluxing [Ir(cod)Cl]2 with 1 and sodium acetate in thf yielded [Ir(C^N^C)(cod)(HgCl)] (4). Chlorination of 4 with PhICl2 gave [Ir(C^N^C)(cod)Cl]·HgCl2 (5·HgCl2) that reacted with tricyclohexylphosphine to yield Hg-free [Ir(C^N^C)(cod)Cl] (5). Chloride abstraction of 5 with silver(i) triflate (AgOTf) gave [Ir(C^N^C)(cod)(H2O)](OTf) (6) that can catalyze the cyclopropanation of styrene with ethyl diazoacetate. Reaction of 1 and [Ir(CO)2Cl(py)] (py = pyridine) with sodium acetate in refluxing thf afforded [Ir(C^N^C)(HgCl)(py)(CO)] (7), in which the carbonyl ligand is coplanar with the C^N^C ligand. On the other hand, refluxing 1 with (PPh4)[Ir(CO)2Cl2] and sodium acetate in acetonitrile gave [Ir(C^N^C)(κ2C,N-HC^N^C)(CO)] (8), the carbonyl ligand of which is trans to the pyridyl ring of the bidentate HC^N^C ligand. Upon irradiation with UV light 8 in thf was isomerized to 8', in which the carbonyl is trans to a phenyl group of the bidentate HC^N^C ligand. The isomer pair 8 and 8' exhibited emission at 548 and 514 nm in EtOH/MeOH at 77 K with lifetime of 84.0 and 64.6 µs, respectively. Protonation of 8 with p-toluenesulfonic acid (TsOH) afforded the bis(bidentate) tosylate complex [Ir(κ2C,N-HC^N^C)2(CO)(OTs)] (9) that could be reconverted to 8 upon treatment with sodium acetate. The electrochemistry of the Ir(C^N^C) complexes has been studied using cyclic voltammetry. Reaction of [Ir(PPh3)3Cl] with 1 and sodium acetate in refluxing thf led to isolation of the previously reported compound [Ir(κ2P,C-C6H4PPh2)2(PPh3)Cl] (10). The crystal structures of 2-5, 8, 8', 9 and 10 have been determined.
RESUMO
The treatment of HfCl(4) with NaL(OEt) (L(OEt)(-) = [(eta(5)-C(5)H(5))Co{P(O)(OEt)(2)}(3)](-)) in nitric acid afforded L(OEt)Hf(NO(3))(3) (1). Hydrolysis of 1 in acetone/water (4:1, v/v) yielded the hydroxy-bridged dimer [(L(OEt))(2)Hf(2)(H(2)O)(4)(mu-OH)(2)][NO(3)](4) (2). The treatment of (NH(4))(2)[Ce(NO(3))(6)] with 2 equiv of NaL(OEt) in water afforded (L(OEt))(2)Ce(NO(3))(2) (3), whereas that with 1 equiv of NaL(OEt) in CH(2)Cl(2) gave L(OEt)Ce(NO(3))(3) (4). While 4 is stable in organic solvents such as acetone, it was converted completely to 3 in acetone/water. The treatment of 3 with bis(p-nitrophenyl)phosphate (BNPP) afforded (L(OEt))(2)Ce[eta(1)-OPO(OR)(2)](2) (5; R = p-NO(2)C(6)H(4)), whereas the reaction of 4 with NaPO(2)(OR)(2) yielded dinuclear [L(OEt)Ce(NO(3))(2){mu-O(2)P(OR)(2)}](2) [R = p-NO(2)C(6)H(4) (6), Ph (7)]. The addition of 3 in acetone to an aqueous solution of NaH(2)PO(4) yielded the cerium(IV) dihydrogen phosphate complex (L(OEt))(2)Ce(PO(4)H(2))(2) (8). Complexes 1-5 and 7 have been characterized by X-ray crystallography. The hydrolysis of BNPP with L(OEt)M(NO(3))(3) (M = Zr, Hf, Ce) in acetone/water has been studied by (1)H NMR spectroscopy. At 25 degrees C, with [Ce] = 20[BNPP], in an acetone-d(6)/N-(2-hydroxyethyl)piperazine-N'-2-ethanesulfonic acid (4:1, v/v) buffer solution (50 mM) (4:1, v/v), the hydrolysis of BNPP with 4 was found to exhibit first-order kinetics with a rate constant of (1.1 +/- 0.1) x 10(-3) s(-1).
Assuntos
Cério/química , Háfnio/química , Nitrofenóis/química , Compostos Organometálicos/química , Oxigênio/química , Ésteres/química , Hidrólise , LigantesRESUMO
The treatment of a slurry of an equimolar mixture of [Sn(edt)(2)] (edt = ethane-1,2- dithiolate) and [Et(4)N]Cl.xH(2)O with CuI in the presence of PPh(3) gave a tetranuclear compound, [Sn(edt)(2)Cl(mu-I)(mu(3)-I)(CuPPh(3))(3)] (1), which consists of a rectangular-pyramidal [Sn(edt)(2)Cl](-) moiety ligated by three [Cu(PPh(3))](+) fragments via the sulfur atoms of the edt(2-) ligands. The treatment of a slurry of [Sn(edt)(2)] and excess [Et(4)N]Br with [Cu(MeCN)(4)][PF(6)] in the presence of PPh(3) afforded a pentanuclear compound, [Sn(edt)(2)(mu-Br)(2)(mu(3)-Br)(2)(CuPPh(3))(4)] (2), which comprises two [(CuPPh(3))(2)(mu-Br)](+) fragments symmetrically ligating an octahedral trans-[Sn(edt)(2)Br(2)](2-) moiety via the sulfur and bromide atoms. Reaction of [Sn(edt)(2)] with [Cu(MeCN)(4)][PF(6)] and PPh(3) in a mixed MeCN/CH(2)Cl(2) solution yielded a novel octanuclear compound, [{Sn(edt)(2)}(3)(mu-OH)(3)Cu(5)(PPh(3))(8)][PF(6)](2) (3), which may be described as a triangular [{Sn(edt)(2)}(3)(mu-OH)(3)](3-) core chelated by three [Cu(PPh(3))(2)](+) species and capped by two [Cu(PPh(3))](+) species. The luminescent properties of compounds 1, 2, and 3 were investigated in a CH(2)Cl(2) solution at room temperature. Upon excitation at lambda > 360 nm, these compounds are luminescent in CH(2)Cl(2) solution with emissions having maxima at 422, 515, and 494 nm, respectively.
RESUMO
Iridium porphyrin complexes containing µ-nitrido, hydroxo, hydrosulfido, and alkynyl ligands have been synthesized and structurally characterized, and their oxidation has been studied. The alkyl-IrIII porphyrin complex [Ir(tpp)R] (tpp2- = 5,10,15,20-tetraphenylporphyrin dianion; R = C8H13; 1) was synthesized by reaction of [Ir(cod)Cl]2 (cod = 1,5-cyclooctadiene) with H2tpp in refluxing monoethylene glycol. Treatment of 1 with PPh3 and [(LOEt)Ru(N)Cl2] (LOEt- = [(η5-C5H5)Co{P(O)(OEt)2}3]-) gave [Ir(tpp)(R)(PPh3)] (2) and the µ-nitrido complex [R(tpp)Ir(µ-N)RuCl2(LOEt)] (3), respectively. The cyclic voltammogram of 3 exhibited a reversible oxidation couple at 0.44 V versus Fc+/0 (Fc = ferrocene). The oxidation of 3 with [(4-BrC6H4)3N](SbCl6) resulted in Ir-C bond homolysis and formation of the chloride complex [Cl(tpp)Ir(µ-N)RuCl2(LOEt)] (4). The short Ir-N(nitrido) bond distances in 3 [1.944(3) Å] and 4 [1.831(4) Å] are indicative of multiple bond character and thus these two µ-nitrido complexes can be described by the two resonance forms: IrIII-N[triple bond, length as m-dash]RuVI and IrV[double bond, length as m-dash]N[double bond, length as m-dash]RuIV. Similarly, the oxidation of 2 with [(4-BrC6H4)3N](SbCl6) yielded [Ir(tpp)Cl(PPh3)] (5). Chloride abstraction of 5 with TlPF6 in tetrahydrofuran (thf) afforded [Ir(tpp)(PPh3)(thf)](PF6) (6) that reacted with CsOH·H2O and Li2S to give the hydroxo [Ir(tpp)(OH)(PPh3)] (7) and hydrosulfido [Ir(tpp)(PPh3)(SH)] (8) complexes, respectively. Treatment of 6 with phenylacetylene in the presence of CuI and Et3N yielded the bimetallic complex [Ir(tpp)(PPh3)(µ-η1:η2-C[triple bond, length as m-dash]CPh)(CuI)] (9), whereas the transmetallation of 6 with LiC[triple bond, length as m-dash]CPh afforded the mononuclear alkynyl complex [Ir(tpp)(PPh3)(C[triple bond, length as m-dash]CPh)] (10). The electrochemistry of the Ir porphyrin complexes has been studied using cyclic voltammetry. On the basis of the measured redox potentials of [Ir(tpp)(PPh3)X], the ability of X- to stabilize the IrIV state is ranked in the order: R- > PhC[triple bond, length as m-dash]C- > Cl- â¼ OH-. Oxidation of 8 and 9 with [(4-BrC6H4)3N](SbCl6) led to isolation of 5 and [Ir(tpp)(PPh3)(H2O)]+, respectively. The crystal structures of complexes 3, 4, and 7-10 have been determined.
RESUMO
In an attempt to synthesize heterometallic cerium nitrido complexes, we studied the reactions of cerium complexes supported by the Kläui tripodal ligand [Co(η5-C5H5){PO(OEt)2}3]- (LOEt-) with transition-metal nitrides. Whereas no reactions were found between Ce-LOEt complexes and [RuVI(LOEt)(N)Cl2] (2), treatment of the Ce(iv) oxo complex [CeIV(LOEt)2(O)(H2O)]·MeCONH2 (1) with 2 resulted in reduction of both the Ce(iv) and Ru(vi) complexes, and formation of a heterometallic Ce(iii)/Ru(iii) complex with a bridging deprotonated acetamide ligand, [(LOEt)2(H2O)CeIII{µ-O,N-MeC(O)NH}RuIII(LOEt)Cl2] (4), along with a minor product, [CeIII(LOEt)2(NO3)]. Ce(iv)-LOEt complexes such as [CeIV(LOEt)2Cl2] (3) can oxidize [ReV(LOEt)(N)(PPh3)Cl] to give the Re(vi) nitride [ReVI(LOEt)(N)(PPh3)Cl]+. Chloride abstraction of 3 by TlPF6 followed by reaction with [PPh4]2[MnV(N)(CN)4] afforded a diamagnetic red solid that is tentatively formulated as a heterometallic Ce(iv)/Mn(v) complex, [Ce(LOEt)2(H2O){Mn(N)(CN)4}] (5). Reactions of 3 with [nBu4N][MVI(N)(cat)2] (cat2- = catecholate(2-)) afforded the Ce(iii)/M(vi) complexes [(LOEt)2CeIII{(µ-cat)2MVI(N)}] [M = Ru (6), Os (7)], in which the Ce(iii) and M(vi) centers are bridged by two oxygen atoms of the two catecholate ligands. Similarly, the catecholate-bridged Ce(iii)/Re(v) complex [(LOEt)2CeIII{(µ-cat)2ReV(O)}] (8) was prepared from 3 and [Me4N][ReV(O)(cat)2]. In CH2Cl2, 8 was air-oxidized to the Ce(iii)/Re(vii) complex [CeIII(LOEt)2(H2O)2][cis-{ReVII(O)2(cat)2}] (9) with a cis-dioxo-Re(vii) counter-anion. The crystal structures of 4, 6, and 9 have been determined.
RESUMO
The 4-coordinated RuII chalcogenolate complexes [Ru(STipp)2(PPh3)2] (Tipp = 2,4,6-triisopropylphenyl, 1) and [Ru(SeMes)2(PPh3)2] (Mes = 2,4,6-trimethylphenyl, 2) have been synthesized, and their reactions with PhICl2 and organic azides have been studied. Complex 2 synthesized from [RuII(PPh3)3Cl2] and NaSeMes displays a seesaw structure with P-Ru-P and Se-Ru-Se bond angles of 103.43(13) and 145.26(6)°, respectively. Natural bond order analyses revealed that in each of 1 and 2, there are two n âσ* (donor-acceptor) π interactions between the chalcogen lone pairs and the Ru-P antibonding molecular orbitals. The calculated second-order perturbation interaction energies of the two interactions for 1 (20.5 and 18.3 kcal mol-1) are stronger than those of 2 (13.6 and 11.0 kcal mol-1), suggesting the thiolate ligand (TippS-) is a stronger π-donor than the selenolate ligand (MesSe-) with respect to RuII. Chlorination of 1 with PhICl2 afforded the dichloride complex [Ru(STipp)2Cl2(PPh3)] (3), which was hydrolyzed to the hydroxo complex [Ru(STipp)2(OH)Cl(PPh3)] (4) after column chromatography on silica in air. Treatment of 4 with HCl and methyl triflate gave 3 and [Ru(STipp)2(OH)(OTf)(PPh3)] (OTf = triflate, 5), respectively. Reactions of 1 and 2 with p-tolyl azide (p-tolN3) afforded the tetrazene complexes [Ru{N4(p-tol)2}(ER)2(PPh3)] (ER = STipp (6), SeMes (7)), whereas that with tosyl azide (TsN3) gave the imido complexes [Ru(κ2-NTs)(STipp)2(PPh3)] (ER = STipp (8), SeMes (10)). The short Ru-Nimido distances in 8 [1.883(3) Å] and 10 [1.892(2) Å] are indicative of multiple bond character. Treatment of 8 with TsN3 afforded the tetrazene complex [Ru(N4Ts2)(STipp)2(PPh3)] (9), but no cycloaddition was found between 10 and TsN3. Nucleophilic attack of the imido ligand in 10 with methyl triflate yielded the amido complex [Ru(κ2-NMeTs)(SeMes)2(PPh3)](OTf) (11). The crystal structures of 2, 4, 6, and 8-11 have been determined.