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1.
Harriman A Mayeux A Stroh C Ziessel R 《Dalton transactions (Cambridge, England : 2003)》2005,(17):2925-2932
A binuclear complex has been synthesized having ruthenium(ii) bis(2,2':6',2'-terpyridine) terminals attached to a central 2,2'-bipyrimidine unit via ethynylene groups. Cyclic voltammetry indicates that the substituted terpyridine is the most easily reduced subunit and the main chromophore involves charge transfer from the metal centre to this ligand. The resultant metal-to-ligand, charge-transfer (MLCT) triplet state is weakly emissive and has a lifetime of 60 ns in deoxygenated solution at room temperature. The luminescence yield and lifetime increase with decreasing temperature in a manner that indicates the lowest-energy MLCT triplet couples to at least two higher-energy triplets. Cations can bind to the central bipyrimidine unit, forming both 1:1 and 1:2 (ligand:metal) complexes as confirmed by electrospray MS analysis. The photophysical properties depend on the number of bound cations and on the nature of the cation. In the specific case of binding zinc(ii) cations, the 1:1 complex has a triplet lifetime of 8.0 ns while that of the 1:2 complex is 1.8 ns. The 1:1 complexes formed with Ba(2+) and Mg(2+) are more luminescent than is the parent compound while the 1:2 complexes are much less luminescent. It is shown that the coordinated cations raise the reduction potential of the central bipyrimidine unit and thereby increase the activation energy for coupling with the metal-centred state. Complexation also introduces a non-emissive intramolecular charge-transfer (ICT) state that couples to the lowest-energy MLCT triplet and provides an additional non-radiative decay route. The triplet state of the 1:2 complex formed with added Zn(2+) cations decays preferentially via this ICT state. 相似文献
2.
Benniston AC Harriman A Li P Sams CA Ward MD 《Journal of the American Chemical Society》2004,126(42):13630-13631
A series of binuclear ruthenium(II)-bis(2,2':6',2' '-terpyridine) complexes has been prepared around a central biphenylene unit equipped with a strap of variable length. Partial oxidation forms the mixed-valence complex that displays both ligand-to-metal, charge-transfer, and intervalence charge-transfer (IVCT) transitions in the near-IR region. On the basis of Hush theory, the electronic coupling matrix element for interaction between the metal centers decreases with increasing length of the tethering strap. This effect arises because the strap modulates the torsion angle between the phenyl rings and thereby controls the extent of through-bond electronic coupling. The coupling element favors a maximum for planar geometries and a minimum for orthogonal structures, but the full impact of the torsion angle is not realized due to thermal fluctuations. 相似文献
3.
Benniston AC Harriman A Romero FM Ziessel R 《Dalton transactions (Cambridge, England : 2003)》2004,(8):1233-1238
The photophysical properties of closely-coupled, binuclear complexes formed by connecting two ruthenium(II) tris(2,2'-bipyridine) complexes via an alkynylene group differ significantly from those of the relevant mononuclear complex. In particular, the energy of the first triplet excited state is lowered relative to the parent complex, because of the presence of the alkynylene substituent, while the triplet lifetime is prolonged, in part, because of extended electron delocalization. We now report that the triplet lifetime is also affected by the nature of the spectator 2,2'-bipyridyl ligands. Thus, replacing the parent 2,2'-bipyridine ligands with the corresponding 4,4'-dinitro-substituted ligands serves to decrease the luminescence yield and lifetime. With the corresponding carboxylate ester, the luminescence yield and lifetime are increased. Perdeuteration of the parent 2,2'-bipyridine ligands also leads to a modest increase in the luminescence yield. Such observations are indicative of electronic coupling between the various metal-to-ligand, charge-transfer excited triplet states. Temperature dependence studies confirm that these excited states are closely spaced and thermally accessible at ambient temperature. For some of the binuclear complexes, the quantum yield for formation of the lowest-energy triplet state is significantly less than unity. 相似文献
4.
Benniston AC Harriman A Li P Patel PV Rostron JP Sams CA 《The journal of physical chemistry. A》2006,110(32):9880-9886
The photophysical properties are reported for a series of binuclear ruthenium(II) bis(2,2':6',2"-terpyridine) complexes built around a geometrically constrained, biphenyl-based bridge. The luminescence quantum yield and lifetime increase progressively with decreasing temperature, but the derived rate constant for nonradiative decay of the lowest-energy triplet state depends on the length of a tethering strap attached at the 2,2'-positions of the biphenyl unit. Since the length of the strap determines the dihedral angle for the central C-C bond, the rate of nonradiative decay shows a pronounced dependence on angle. The minimum rate of nonradiative decay occurs when the dihedral angle is 90 degrees, but there is a maximum in the rate when the dihedral angle is about 45 degrees. This effect does not appear to be related to the extent of electron delocalization at the triplet level but can be explained in terms of variable coupling with a low-frequency vibrational mode associated with the strapped biphenyl unit. 相似文献
5.
Synthesis and properties of the elusive ruthenium(II) complexes of 4'-cyano-2,2':6',2' '-terpyridine
The heteroleptic and homoleptic ruthenium(II) complexes of 4'-cyano-2,2':6',2' '-terpyridine are synthesized by palladium catalyzed cyanation of the corresponding Ru(II) complexes of 4'-chloro-2,2':6',2' '-terpyridine. The introduction of the strongly electron-withdrawing cyano group into the Ru(tpy)(2)(2+) moiety dramatically changes its photophysical and redox properties as well as prolongs its room temperature excited-state lifetime. 相似文献
6.
An electroactive luminescent switch has been synthesized that comprises a hydroquinone-functionalized 2,2':6',2'-terpyridine ligand coordinated to a ruthenium(II) (4'-phenylethynyl-2,2':6',2'-terpyridine) fragment. The assembly is sufficiently rigid that the hydroquinone-chromophore distance is fixed. Excitation of the complex via the characteristic metal-to-ligand charge-transfer (MLCT) absorption band produces an excited triplet state in which the promoted electron is localized on the terpyridine ligand bearing the acetylenic group. The triplet lifetime in butyronitrile solution at room temperature is 46 +/- 3 ns but increases markedly at lower temperature. Oxidation of the hydroquinone to the corresponding benzoquinone switches on an electron-transfer process whereby the MLCT triplet donates an electron to the quinone. This reaction reduces the triplet lifetime to 190 +/- 12 ps and essentially extinguishes emission. The rate of electron transfer depends on temperature in line with classical Marcus theory, allowing calculation of the electronic coupling matrix element and the reorganization energy as being 22 cm(-1) and 0.84 eV, respectively. The switching behavior can be monitored using luminescence spectroelectrochemistry. The on/off level is set by temperature and increases as the temperature is lowered. 相似文献
7.
A small series of ruthenium(II) tris(2,2'-bipyridine) complexes has been synthesized in which ethynylated thiophene residues are attached to one of the 2,2'-bipyridine ligands. The photophysical properties depend on the conjugation length of the thiophene-based ligand, and in each case, dual emission is observed. The two emitting states reside in thermal equilibrium at ambient temperature and can be resolved by emission spectral curve-fitting routines. This allows the properties of the two states to be evaluated in both fluid butyronitrile solution and a transparent KBr disk. It is concluded that both emitting states are of metal-to-ligand charge-transfer (MLCT) character, and despite the presence of conjugated thiophene residues, there is no indication for a low-lying pi,pi*-triplet state that promotes nonradiative decay of the excited-state manifold. A key feature of these systems is that the conjugation length imposed by the thiophene-based ligand helps to control the rate constants for both radiative and nonradiative decay from the two MLCT triplet states. 相似文献
8.
Constable EC Dunphy EL Housecroft CE Neuburger M Schaffner S Schaper F Batten SR 《Dalton transactions (Cambridge, England : 2003)》2007,(38):4323-4332
Ligands in which multiple metal-binding domains are linked by a metal-containing moiety rather than a conventional organic group are described as "expanded ligands". The use of 4,4'-difunctionalised {Ru(tpy)(2)} units provides a linear spacer between metal-binding domains and we have extended this motif to expanded ligands containing two carboxylic acid metal-binding domains. In this paper, we describe the synthesis and structural characterisation of ruthenium(ii) complexes of 2,2':6',2'-terpyridine-4'-carboxylic acid and 4'-carboxyphenyl-2,2':6',2'-terpyridine. The ability of the ruthenium(ii) centre to charge compensate deprotonation of the carboxylic acid leads to Zwitterionic complexes and three representative compounds have been structurally characterised. 相似文献
9.
Photophysical properties have been recorded for a ruthenium(II) bis(2,2':6',2' '-terpyridine) complex bearing a single ethynylene substituent. The target compound is weakly emissive in fluid solution at room temperature, but both the emission yield and lifetime increase dramatically as the temperature is lowered. As found for the unsubstituted parent complex, the full temperature dependence indicates that the lowest-energy triplet state couples to two higher-energy triplets and to the ground state. Luminescence occurs only from the lowest-energy triplet state, but the radiative and nonradiative decay rates indicate that electron delocalization occurs at the triplet level. Comparison of the target compound with the parent complex indicates that the ethynylene group reduces the size of the electron-vibrational coupling element for nonradiative decay of the lowest-energy triplet state. Although other factors are affected by substitution, this is by far the most important feature with regard to stabilization of the triplet state. 相似文献
10.
A series of RuII or FeII trischelate complex salts containing N-methyl/aryl-2,2':4,4' ':4',4' '-quaterpyridinium ligands that has previously been subjected to quadratic nonlinear optical studies (Coe, B. J. et al. J. Am. Chem. Soc. 2005, 127, 13399) has now been investigated for two-photon absorbing behavior. Z-scan measurements using a 750 nm laser afford reasonably large two-photon absorption (2PA) cross-sections sigma2 of ca. 62-180 GM for the RuII complexes, but only very weak 2PA is observed for the FeII compounds. The excited-state and 2PA properties of the representative chromophore [RuII(Me2Qpy2+)3]8+ (Me2Qpy2+=N' ',N' '-dimethyl-2,2':4,4' ':4',4' '-quaterpyridinium) have also been investigated by using semiempirical intermediate neglect of differential overlap/multireference-determinant single and double configuration interaction computations with the optimized geometry obtained via density functional theory. The calculated sigma2 value of ca. 624 GM at 1.70 eV for this metal-to-ligand charge-transfer chromophore is about 10 times larger than that obtained from the Z-scan studies. 相似文献
11.
Chow HS Constable EC Housecroft CE Neuburger M Schaffner S 《Dalton transactions (Cambridge, England : 2003)》2006,(23):2881-2890
The synthesis and characterisation of five new ligands (L), each containing a terpy binding domain and bearing a pendant naphthalene group in the 4'-position are described; homoleptic complexes, [ML2][PF6]4 (M = Fe, Ru) have been studied and structural data for four complexes are reported. 相似文献
12.
Chow HS Constable EC Housecroft CE Kulicke KJ Tao Y 《Dalton transactions (Cambridge, England : 2003)》2005,(2):236-237
Electron exchange between [Co(terpy)2]3+ and [Co(terpy)2]2+ can be monitored by 1H NMR exchange spectroscopy and allows the cobalt(II) spectra to be fully assigned. 相似文献
13.
Newkome GR Yoo KS Kim HJ Moorefield CN 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(14):3367-3374
Routes for the syntheses of isomeric, zwitterionic, bisterpyridine-Ru(II)-based macromolecules are described. Access to these novel architectures is facilitated by the construction of terpyridine-modified, 1-->3 C-branched, ester-terminated building blocks. Constitutional isomers result from the interchangable placement of methyl and tert-butyl ester groups on both the branched framework near the Ru(II) centers and the termini of the branched construct. Water solubility is imparted to each isomer through selective transformation of the tert-butyl esters to their corresponding carboxylates. Along with the standard characterization techniques, electrochemical and spectroscopic data also support the structural formation. 相似文献
14.
Anthonysamy A Balasubramanian S Shanmugaiah V Mathivanan N 《Dalton transactions (Cambridge, England : 2003)》2008,(16):2136-2143
The synthesis and characterization of Ru(II) terpyridine complexes derived from 4'-functionalized 2,2':6',2'-terpyridine ligands by a multi step procedure have been described. The complexes are redox-active, showing both metal-centred (oxidation) and ligand-centred (reduction) processes. The antibacterial and antifungal activity of the synthesized ruthenium(II) complexes [Ru(attpy)2](PF6)2 (attpy = 4'-(4-acryloyloxymethylphenyl)-2,2':6',2'-terpyridine); [Ru(mttpy)2](PF6)2 (mttpy = 4'-(4-methacryloyloxymethylphenyl)-2,2':6',2'- terpyridine); [Ru(mttpy)(MeOPhttpy)](PF6)2 (MeOPhttpy = 4'-(4-methoxyphenyl)-2,2':6',2'-terpyridine); and [Ru(mttpy)(ttpy)](PF6)2 (ttpy = 4'-(4-methylphenyl)-2,2':6',2'-terpyridine) were tested against four human pathogens (Proteus vulgaris, Proteus mirabilis, Pseudomonas aeruginosa and Escherichia coli) and five plant pathogens (Curvularia lunata, Fusarium oxysporum, Fusarium udum, Macrophomina phaseolina and Rhizoctonia solani) by the well diffusion method and MIC values of the complexes are reported. A biological study of the complexes indicated that the complexes [Ru(mttpy)2](PF6)2 and [Ru(mttpy)(MeOPhttpy)](PF6)2 exhibit very good activity against most of the test pathogens and their activity is better than those of some of the commercially available antibiotics like tetracycline and the fungicide carbendazim. 相似文献
15.
The synthesis and photophysical and electrochemical properties of tris(homoleptic) complexes [Ru(tpbpy)3](PF6)2 (1) and [Os(tpbpy)3](PF6)2 (2) (tpbpy = 6'-tolyl-2,2':4',2' '-terpyridine) are reported. The ligand tpbpy is formed as the side product during the synthesis of 4'-tolyl-2,2':6',2' '-terpyridine (ttpy) and characterized by single-crystal X-ray diffraction: monoclinic, P21/c. The tridentate tpbpy coordinates as a bidentate ligand. The complexes 1 and 2 exhibit two intense absorption bands in the UV region (200-350 nm) assignable to the ligand-centered (1LC) pi-pi* transitions. The ruthenium(II) complex exhibits a broad absorption band at 470 nm while the osmium(II) complex exhibits an intense absorption band at 485 nm and a weak band at 659 nm assignable to the MLCT (dpi-pi*) transitions. A red shifting of the dpi-pi* MLCT transition is observed on going from the Ru(II) to the Os(II) complex as expected from the high-lying dpi Os orbitals. These complexes exhibit ligand-sensitized emission at 732 and 736 nm, respectively, upon light excitation onto their MLCT band through excitation of higher energy LC bands at room temperature. The MLCT transitions and the emission maxima of 1 and 2 are substantially red-shifted compared to that of [Ru(bpy)3](PF6)2 and [Os(bpy)3](PF6)2. The emission of both the complexes in the presence of acid is completely quenched indicating that the emission is not due to the protonation of the coordinated ligands. Our results indicate the occurrence of intramolecular energy transfer from the ligand to the metal center. Both the complexes undergo quasi-reversible metal-centered oxidation, and the E1/2 values for the M(II)/M(III) redox couples (0.94 and 0.50 V versus Ag/Ag+ for 1 and 2, respectively) are cathodically shifted with respect to that of [Ru(bpy)3](PF6)2 and [Os(bpy)3](PF6)2 (E1/2 = 1.28 and 1.09 V versus Ag/Ag+, respectively). The tris(homoleptic) Ru(II) and Os(II) complexes 1 and 2 could be used to construct polynuclear complexes by using the modular synthetic approach in coordination compounds by exploiting the coordinating ability of the pyridine substituent. Furthermore, these complexes offer the possibility of studying the influence of electron-withdrawing and electron-donating substituents on the photophysical properties of Ru(II) and Os(II) polypyridine complexes. 相似文献
16.
The photophysical properties of osmium(II) bis(2,2':6',2' '-terpyridine) have been recorded over a wide temperature range. An emission band is observed and attributed to radiative decay of the lowest-energy metal-to-ligand, charge-transfer (MLCT) triplet state. This triplet is coupled to two other triplet states that lie at higher energy. The second triplet, believed to be of MLCT character, is reached by crossing a barrier of only 640 cm(-1), but the highest-energy triplet, considered to be of metal-centered (MC) character, is separated from the lowest-energy MLCT triplet by a barrier of 3500 cm(-1). Analysis of the emission spectrum shows that both low- and high-frequency modes are involved in the decay process, while weak emission is seen from the second excited triplet state. The magnitude of the low- and high-frequency modes depends on temperature in fluid solution but not in a KBr disk. Apart from a substantial lowering of the triplet energy, the photophysical properties are relatively insensitive to the presence of an ethynylene substituent at the 4' position of each terpyridine ligand. However, the barrier to reaching the MC triplet is markedly reduced, and the vibrational modes become less sensitive to changes in temperature. 相似文献
17.
Benniston AC Harriman A Pariani C Sams CA 《Physical chemistry chemical physics : PCCP》2006,8(17):2051-2057
A molecular triad has been synthesized comprising two free-base porphyrin terminals linked to a central ruthenium(II) bis(2,2':6',2'-terpyridine) subunit via meso-phenylene groups. Illumination into the ruthenium(II) complex is accompanied by rapid intramolecular energy transfer from the metal-to-ligand, charge-transfer (MLCT) triplet to the lowest-energy pi-pi* triplet state localized on one of the porphyrin subunits. Transfer takes place from a vibrationally excited level which lowers the activation energy. The electronic coupling matrix element for this process is 73 cm(-1). Selective illumination into the lowest-energy singlet excited state (S1) localized on the porphyrin leads to fast singlet-triplet energy transfer that populates the MLCT triplet state with high efficiency. This latter process occurs via Dexter-type electron exchange at room temperature, but the activation energy is high and the reaction is prohibited at low temperature. For this latter process, the electronic coupling matrix element is only 8 cm(-1). 相似文献
18.
Beves JE Dunphy EL Constable EC Housecroft CE Kepert CJ Neuburger M Price DJ Schaffner S 《Dalton transactions (Cambridge, England : 2003)》2008,(3):386-396
A comparative structural and spectroscopic investigation of the complexes [M(1)2]2+, [M(2)2]2+ and [M(3)2]2+ in which M = Fe or Ru, and ligands 1, 2 and 3 are 4'-(2-pyridyl)-, 4'-(3-pyridyl)- and 4'-(4-pyridyl)-2,2':6',2"-terpyridine, respectively, is reported. The complexes [Ru(1)2]2+, [Ru(2)2]2+ and [Ru(3)2]2+ undergo mono- and bis-N-methylation. The consequences of methylation on the absorption spectra and electrochemical properties are discussed; the solid-state structure of the bis(N-methylated) derivative of [Ru(2)2][PF6]2 is presented. 相似文献
19.
A series of novel platinum(II)-2,2':6',2' '-terpyridine (trpy) complexes containing (thioalkyl)dicarba-closo-dodecaborane(12) (closo-carborane) derivatives were prepared by treatment of the labile precursor species [Pt(MeCN)(trpy)](OTf)2 with R(CH2)nSH (R = closo-1,2-carborane, n = 0-3; R = closo-1,7-carborane, n = 1; R = closo-1,12-carborane, n = 1) in the presence of NEt3 to afford brightly colored complexes of the type [PtS(CH2)nR(trpy)]OTf. All products were characterized by means of multinuclear (1H, 13C, 11B, and 195Pt) 1D- and 2D-NMR spectroscopy, ESI-MS, and, for the 1,7-carborane derivative, X-ray crystallography. Preliminary in vitro cytotoxicity studies of selected complexes against human ovarian carcinoma cells are also reported. 相似文献
20.
Fang YQ Taylor NJ Laverdière F Hanan GS Loiseau F Nastasi F Campagna S Nierengarten H Leize-Wagner E Van Dorsselaer A 《Inorganic chemistry》2007,46(7):2854-2863
A series of new tridentate polypyridine ligands, made of terpyridine chelating subunits connected to various substituted 2-pyrimidinyl groups, and their homoleptic and heteroleptic Ru(II) complexes have been prepared and characterized. The new metal complexes have general formulas [(R-pm-tpy)Ru(tpy)]2+ and [Ru(tpy-pm-R)2]2+ (tpy = 2,2':6',2' '-terpyridine; R-pm-tpy = 4'-(2-pyrimidinyl)-2,2':6',2' '-terpyridine with R = H, methyl, phenyl, perfluorophenyl, chloride, and cyanide). Two of the new metal complexes have also been characterized by X-ray analysis. In all the R-pm-tpy ligands, the pyrimidinyl and terpyridyl groups are coplanar, allowing an extended delocalization of acceptor orbital of the metal-to-ligand charge-transfer (MLCT) excited state. The absorption spectra, redox behavior, and luminescence properties of the new Ru(II) complexes have been investigated. In particular, the photophysical properties of these species are significantly better compared to those of [Ru(tpy)2]2+ and well comparable with those of the best emitters of Ru(II) polypyridine family containing tridentate ligands. Reasons for the improved photophysical properties lie at the same time in an enhanced MLCT-MC (MC = metal centered) energy gap and in a reduced difference between the minima of the excited and ground states potential energy surfaces. The enhanced MLCT-MC energy gap leads to diminished efficiency of the thermally activated pathway for the radiationless process, whereas the similarity in ground and excited-state geometries causes reduced Franck Condon factors for the direct radiationless decay from the MLCT state to the ground state of the new complexes in comparison with [Ru(tpy)2]2+ and similar species. 相似文献