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A molecular loop with interstitial channels in a chiral environment and study of formation of metal-metal bonds in dinickel, dipalladium and dititanium complexesIbragimov, Sergey 16 August 2006 (has links)
This dissertation consists of two independent topics: (1) a molecular loop with
interstitial channels in a chiral environment; (2) study of formation of metal-metal bonds
in dinickel, dipalladium and dititanium complexes
On the first topic, a study of the reaction products of the interaction of cis-
Mo2(DAniF)2(CH3CN)4
2+ corner pieces with ortho-, meta- and para- isomers of
enatiomerically pure ÂO2CCH(CH3)C6H4CH(CH3)CO2
 dicarboxylate was performed.
First, an enantiomerically pure molecular loop based on two dimolybdenum units and
two para-dic arboxylate linkers was synthesized and structurally characterized. Similar
reactions with isomeric ortho- and meta- dicarboxylate linkers, as well as with some
nonchiral ligands, showed that the structure of the obtained products depends on the
geometry of the ligand. Meta- dicarboxylate linker favors the formation of the chelated
product and ortho- dicarboxylate linker produces the mixture of chelated molecules and
loops. On the second topic, an investigation of the formation of metal-metal bonds was
performed. Study of the one-electron bond obtained upon oxidation of Ni2
4+ and Pd2
4+ to
Ni2
5+ and Pd2
5+, respectively, was made. The compounds synthesized were studied with
various physical methods, such as X-ray crystallography, UV-visible spectroscopy and
EPR spectroscopy. The nature of oxidized species as well as the dependence of metalmetal
interactions on electron-donating abilities of bridging ligands was studied. It was
shown that oxidation takes place on a metal center. The formation of one-electron bond
in oxidized species is proposed.
Finally formation of Ti2
6+ single bonded compounds by the reduction of two Ti4+
monomers to Ti2
6+ dimer was studied. The nature of the species obtained in solution and
in solid state is discussed. The crystal structure shows the presence of two types of hpp
ligands  chelating and bridging. NMR study of this compound in solution proposes the
rearrangement of this structure to a paddlewheel.
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From X-ray structure factors to electron-density distributionsLouca, P. January 1986 (has links)
No description available.
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Electronic localization versus delocalization: a dimetal approachLiu, Chun Yuan 16 August 2006 (has links)
A series of dimolybdenum compounds having a Mo2
4+ core coordinated by various
ligands, including formamidinate (e.g. DAniF = N, NN-di-p-ansisylformamidinate ), acetate
and/or acetonitrile molecules, have been synthesized as building blocks for the construction
of Mo2-containing supramolecular arrays. Compound Mo2(DAniF)3(O2CCH3) was
specifically designed for the preparation of dimolybdenum pairs, whereas the others meet
the needs of Mo2
4+ units for different geometry settings.
Compounds described by a general formula [Mo2]L[Mo2], where [Mo2] =
[Mo2(DAniF)3]+, have two dimetal units electronically coupled by the central unit L , which
consequently engender significant impact on the redox property and electronic structure of
the molecule. It is found that in the weakly coupled complex system, [Mo2]M(OCH3)4[Mo2]
(M = Zn and Co), the mixed-valence complexes present asymmetric molecular structures
with two distinct [Mo2] units corresponding to be a bond order 4.0 (F2B4*2) and 3.5
(F2B4*1), respectively. EPR and magnetic susceptibility measurements for the doubly
oxidized species show that there is no significant antifferromagnetic spin coupling.
Electron delocalization occurs in the complex system where a N, N'-dimethyloxamidate binds two [Mo2] units within two fused six-membered rings. In this
case, the mixed-valence complex has a symmetric molecular structure, implying that the
odd electron is fully delocalized over two [Mo2]units. Strong metal-metal interaction is also
evidenced by intervalence charge transfer of the mixed-valence species and the diamanetism
of the doubly oxidized complex.
Remarkably, two isomers varying in linkage conformation, namely, alpha and beta, have
been isolated as diaryloxamidate ligands are used as the linker. Studies on the neutral and
the oxidized compounds of the two isomers by employing various techniques consistently
show that in the alpha form intramolecular electron transfer is blocked , while in the beta form, the electrons are delocalized over the two [Mo2] units. Thus, the mixed-valence complexes
of the two isomers are appropriately described by alpha-[Mo2]0(oxamidate)[Mo2]1+ and beta-
[Mo2]0.5+(oxamidate)[Mo2]0.5+ respectively.
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Magnetism, Reactivity and Metal Ion Lability in Trigonal Iron ClustersEames, Emily 12 September 2012 (has links)
Important reactions are catalyzed by enzymes employing polynuclear cofactors, often characterized by weak-field ligands and transition metal ions within the sum of the van der Waals radii. While the overall stoichiometries and, in many cases, the structures, of the cofactors are known, the roles of the individual metal ions remain uncertain. Our approach is to investigate model clusters stabilized by a hexadentate, trinucleating ligand. The hexaamine ligand \((MeC (CH_2NHC_6H_4-o-NHPh)_3) (^{Ph}LH_6)\) allows facile synthesis of the clusters \((^{Ph}L)Fe_3(thf)_3\), \((^{Ph}L)Fe_3 (py)_3\), and \((^{Ph}L)Fe_3(PMe_2Ph)_3\) (thf = tetrahydrofuran, py = pyridine). The phenyl substituents on the ligand sterically prevent strong M–M bonding, but permit weaker M–M orbital interactions, with Fe–Fe distances near those found in Fe metal. The complex \((^{Ph}L)Fe_3(thf)_3\) exhibits a well-isolated S = 5 or S = 6 ground state over 5 - 300 K, as evidenced by magnetic susceptibility and reduced magnetization data. However, in the stronger-field pyridine and phosphine complexes, temperature dependent susceptibility is observed which is best modeled as a spin state transition from S = 2 to S = 4. Variable-temperature crystallography and Mössbauer spectroscopy reveal a whole-molecule, rather than site-isolated, spin transition. The all-ferrous cluster \((^{Ph}L)Fe_3(thf)_3\) can be oxidized with triphenylmethyl halides or iodine to give singly-oxidized clusters of the form \((^{Ph}L)Fe_3X(L)\) and \([(^{Ph}L)Fe_3(\mu-X)]_2 (X = Cl, Br, I; L = thf, py)\), in which one Fe–Fe distance contracts to 2.30 Å and the others lengthen to 2.6-2.7 Å. The halide and solvent ligands coordinate a unique Fe, but Mössbauer spectroscopy shows that the diiron pair bears the oxidation. Magnetic data can be modeled by considering a high-spin ferrous ion ferromagnetically coupled to an \(S = 3/2 [Fe_2]^{5+}\) unit. When \([(^{Ph}L)Fe_3(\mu-Cl)]_2\) is reacted with two or five equivalents of \(CoCl_2\) in tetrahydrofuran, the fully-substituted complexes \((^{Ph}L)Fe_2CoCl(acn)\) and \((^{Ph}L)FeCo_2Cl(acn)\) (acn = acetonitrile) can be isolated. \(^1H\) nuclear magnetic resonance shows that they are distinct species, not a mixture, and the elemental ratios are confirmed by X-ray fluorescence spectroscopy. Mössbauer spectroscopy shows that the Co preferentially substitutes into the \([M_2]^{5+}\) unit, as the ferrous site doublet is completely absent in \((^{Ph}L)FeCo_2Cl(acn)\). / Chemistry and Chemical Biology
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The Synthesis of Linear and Nonlinear Photosensitive Organometallic Polymers Containing Mo-Mo Bonds: Evaluating the Effectiveness of Click ChemistryBrady, Sarah 03 October 2013 (has links)
This dissertation details the use of click chemistry to prepare linear and nonlinear polymers containing metal-metal bonds. The incorporation of metal-metal bonds into the polymer simplfies the degradation mechanism, allowing fundamental mechanistic studies of polymer degradation. Click chemistry offered a brand new route to explore the preparation of these useful but intricate metal-metal bond-containing polymers.
Chapter I discusses the utility of these types of polymers for mechanistic studies, the preparation of metal dimers with reactive functionalities, and the previous polymerization methods which have been explored. The need for a new polymerization strategy, such as click chemistry, is described. Chapter II explains the preparation of a new metal dimer click synthon, [(η5-C5H4(CH2)3OC(O)(CH2)2C≡CH)Mo(CO)3]2, and the necessary conditions needed to polymerize the synthon using click chemistry. A high molecular weight linear polymer was prepared, suggesting click chemistry is a viable route to nonlinear polymers.
Chapter III presents a second novel metal dimer click synthon, [(η5-C5H4(CH2)3N3Mo(CO)3]2, and attempts to use click chemistry to prepare a star polymer containing metal-metal bonds. A small amount of nonlinear polymer was prepared but several reactivity problems were also discovered and addressed. Due to these problems with click chemistry, Chapter IV details a brand new method for preparing asymmetric metal dimers. CpMo(CO)3-Mo(CO)3Cp(CH2)3CH=CH2 is the first reported example of an asymmetric dimer, and (CH3)3CSi(CH3)2O(CH2)3CpMo(CO)3-Mo(CO)3Cp(CH2)3OC(CH3)2OCH3 is the first example of a bifunctional asymmetric dimer.
Chapter V describes the synthesis of a different type of metal dimer, (CH3)2Si[(C5H5)Mo(CO)3]2, which is polymerized by thermal ring opening polymerization. The dimer did not polymerize as expected and yielded an interesting polymer which has both Mo-Mo single bonds and Mo≡Mo triple bonds. Finally, Chapter VI provides a summary of the work as well as an honest perspective of using click chemistry to prepare metal-metal bond-containing polymers.
This dissertation includes previously published and unpublished co-authored material. / 10000-01-01
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On Thallium (III) and binuclear platinum-thallium complexes with N-donor ligands in solution and in solidMa, Guibin January 2001 (has links)
This thesis describes the synthesis, structure, equilibriaand other properties of novel thallium(III) monomeric andplatinum-bonded complexes with nitrogen donor ligandsethylenediamine, diethylenetriamine, triethylenetetramine,porphyrin, 2,2'-bipyridine and 1,10-phenanthroline in solutionand in solid. The existence of three complexes withthe general formula[Tl(en)n]3+(n = 1-3) and their overall stability constantshave been established in pyridine. All three complexes wereidentified by their205Tl and1H NMR chemical shifts and205Tl-1H coupling constants. The formation process of thecomplexes was followed by1H NMR spectroscopy. The crystal structure of[Tl(en)3](ClO4)3was determined; the thallium(III) ion isN-coordinated in a distorted octahedral geometry. Two [Tl(dien)n]3+(n = 1-2) complexes were proved to exist insolution and the structure of the bis-complex [Tl(dien)2]2+inu-facialisomers was determined in solid. In addition,crystal structures of [Tl(en)2CN](ClO4)2with cyanide bridging between two Tl(en)2units forming an infinite chain structure and of[Tl(tren)2(CN)2](ClO4) with a distorted pseudo-octahedral coordinationaround thallium were determined. Thallium(III) complexes with2,2'-bipyridine and 1,10-phenanthroline have been studied inDMSO using205Tl,13C and1H NMR spectroscopy. In addition, aseven-coordinated thallium was found in the crystal structureof [Tl(bipy)3(dmso)](ClO4)3, and six-coordinated thallium in pseudo-octahedralgeometry in [Tl(phen)2Cl2](ClO4). The solvated complex [Tl(dmso)6]3+has been prepared using concentrated aqueoussolution of Tl(ClO4)3by a solvent replacement reaction in DMSO, and thewater-free solid compound [Tl(dmso)6](ClO4)3was crystallized from DMSO. The structure of thecomplex [Tl(dmso)6]3+is a regular octahedron with the Tl-O bonddistance 2.224(3) Å. It represents an easy and secure wayto introduce water-free Tl(III) into organic phase withoutreduction. Through several reactions, novel heteronuclear Pt-Tlcomplexes with the composition [(NC)5Pt-Tl(tpp)]2-, [(NC)5Pt-Tl(thpp)]2-, [(NC)5Pt-Tl(bipy)n](n = 1-2), [(NC)5Pt-Tl(en)n-1](n = 1-3) and [(NC)5Pt-Tl(phen)n](n = 1-2), have been synthesized in solution.Multinuclear NMR (195Pt,205Tl,13C and1H), Raman spectroscopy and X-ray diffraction dataare fully compatible with formation of unsupported Pt-Tl bondedcomplexes both in solution and in solid. The huge1J(195Pt-205Tl) spin-spin coupling constants (48-66 kHz) wereobserved by both195Pt and205Tl NMR spectroscopy in solution and they providea strong evidence of formation of the Pt-Tl bond in solution.In all six determined crystal structures of the Pt-Tl compoundsa very short Pt-Tl bond is found with distances2.6117(5)-2.6375(5) Å. The calculated values of Pt-Tlforce constants (1.38-1.91 N/cm) are characteristic for asingle metal-metal bond. In the Pt-Tl compounds, the oxidation state of the metalions is intermediate between the stable states PtII/PtIVand TlIII/TlI, respectively, and this is reflected by their195Pt and205Tl chemical shifts. It turns out that N-donorligands can really stabilize the Pt-Tl bond both in solutionand in solid. The character of the metal-metal bond anditstheoretical basis are discussed. <b>Keywords:</b>Thallium, Platinum, Cyanide, N-donor ligand,Metal-metal bond, Multinuclear NMR, Raman spectroscopy, X-raydiffraction, Equilibrium, Spin-spin coupling.
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On Thallium (III) and binuclear platinum-thallium complexes with N-donor ligands in solution and in solidMa, Guibin January 2001 (has links)
<p>This thesis describes the synthesis, structure, equilibriaand other properties of novel thallium(III) monomeric andplatinum-bonded complexes with nitrogen donor ligandsethylenediamine, diethylenetriamine, triethylenetetramine,porphyrin, 2,2'-bipyridine and 1,10-phenanthroline in solutionand in solid.</p><p>The existence of three complexes withthe general formula[Tl(en)<sub>n</sub>]<sup>3+</sup>(n = 1-3) and their overall stability constantshave been established in pyridine. All three complexes wereidentified by their<sup>205</sup>Tl and<sup>1</sup>H NMR chemical shifts and<sup>205</sup>Tl-<sup>1</sup>H coupling constants. The formation process of thecomplexes was followed by<sup>1</sup>H NMR spectroscopy. The crystal structure of[Tl(en)<sub>3</sub>](ClO<sub>4</sub>)<sub>3</sub>was determined; the thallium(III) ion isN-coordinated in a distorted octahedral geometry. Two [Tl(dien)<sub>n</sub>]<sup>3+</sup>(n = 1-2) complexes were proved to exist insolution and the structure of the bis-complex [Tl(dien)<sub>2</sub>]<sup>2+</sup>in<i>u-facial</i>isomers was determined in solid. In addition,crystal structures of [Tl(en)<sub>2</sub>CN](ClO<sub>4</sub>)<sub>2</sub>with cyanide bridging between two Tl(en)<sub>2</sub>units forming an infinite chain structure and of[Tl(tren)<sub>2</sub>(CN)<sub>2</sub>](ClO<sub>4</sub>) with a distorted pseudo-octahedral coordinationaround thallium were determined. Thallium(III) complexes with2,2'-bipyridine and 1,10-phenanthroline have been studied inDMSO using<sup>205</sup>Tl,<sup>13</sup>C and<sup>1</sup>H NMR spectroscopy. In addition, aseven-coordinated thallium was found in the crystal structureof [Tl(bipy)<sub>3</sub>(dmso)](ClO<sub>4</sub>)<sub>3</sub>, and six-coordinated thallium in pseudo-octahedralgeometry in [Tl(phen)<sub>2</sub>Cl<sub>2</sub>](ClO<sub>4</sub>).</p><p>The solvated complex [Tl(dmso)<sub>6</sub>]<sup>3+</sup>has been prepared using concentrated aqueoussolution of Tl(ClO<sub>4</sub>)<sub>3</sub>by a solvent replacement reaction in DMSO, and thewater-free solid compound [Tl(dmso)<sub>6</sub>](ClO<sub>4</sub>)<sub>3</sub>was crystallized from DMSO. The structure of thecomplex [Tl(dmso)<sub>6</sub>]<sup>3+</sup>is a regular octahedron with the Tl-O bonddistance 2.224(3) Å. It represents an easy and secure wayto introduce water-free Tl(III) into organic phase withoutreduction.</p><p>Through several reactions, novel heteronuclear Pt-Tlcomplexes with the composition [(NC)<sub>5</sub>Pt-Tl(tpp)]<sup>2-</sup>, [(NC)<sub>5</sub>Pt-Tl(thpp)]<sup>2-</sup>, [(NC)<sub>5</sub>Pt-Tl(bipy)<sub>n</sub>](n = 1-2), [(NC)<sub>5</sub>Pt-Tl(en)<sub>n-1</sub>](n = 1-3) and [(NC)<sub>5</sub>Pt-Tl(phen)<sub>n</sub>](n = 1-2), have been synthesized in solution.Multinuclear NMR (<sup>195</sup>Pt,<sup>205</sup>Tl,<sup>13</sup>C and<sup>1</sup>H), Raman spectroscopy and X-ray diffraction dataare fully compatible with formation of unsupported Pt-Tl bondedcomplexes both in solution and in solid. The huge<sup>1</sup>J(<sup>195</sup>Pt-<sup>205</sup>Tl) spin-spin coupling constants (48-66 kHz) wereobserved by both<sup>195</sup>Pt and<sup>205</sup>Tl NMR spectroscopy in solution and they providea strong evidence of formation of the Pt-Tl bond in solution.In all six determined crystal structures of the Pt-Tl compoundsa very short Pt-Tl bond is found with distances2.6117(5)-2.6375(5) Å. The calculated values of Pt-Tlforce constants (1.38-1.91 N/cm) are characteristic for asingle metal-metal bond.</p><p>In the Pt-Tl compounds, the oxidation state of the metalions is intermediate between the stable states Pt<sup>II</sup>/Pt<sup>IV</sup>and Tl<sup>III</sup>/Tl<sup>I</sup>, respectively, and this is reflected by their<sup>195</sup>Pt and<sup>205</sup>Tl chemical shifts. It turns out that N-donorligands can really stabilize the Pt-Tl bond both in solutionand in solid. The character of the metal-metal bond anditstheoretical basis are discussed.</p><p><b>Keywords:</b>Thallium, Platinum, Cyanide, N-donor ligand,Metal-metal bond, Multinuclear NMR, Raman spectroscopy, X-raydiffraction, Equilibrium, Spin-spin coupling.</p>
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Diruthenium Aryls: Structure, Bonding, and ReactivityAdharsh Raghavan (9174119) 27 July 2020 (has links)
The chemistry of metal–metal (M–M) multiply bonded compounds has fascinated inorganic chemists for a period spanning more than five decades. Since the elucidation of the quadruple bond by Cotton in 1964, thousands of compounds featuring M–M bonds have been isolated and studied. Of these, dinuclear units supported by four bidentate ligands forming a ‘paddlewheel’ motif represent a class of compounds that present unique molecular and electronic structures, and useful electrochemical and magnetic properties.<div><br></div><div>Over the last two and a half decades, our laboratory has focused on studying diruthenium paddlewheel complexes for their easeof preparation, rich electrochemical properties,and remarkable stability. We have isolated a vast number of diverse diruthenium alkynyls in multiple oxidation states, bearing different paddlewheel (equatorial) ligand systems and studied their molecular and electronic structures. Taking advantage of the extended conjugation that exists between the Ru2core and the poly-alkynyl ligand motif, we have also found applications for them in prototypical flash-memory devices. At this juncture, we sought to expand the organometallic chemistry of Ru2to complexes featuring Ru–aryl linkages.<br></div><div><br></div><div>The ‘aryl anion’ is, based on pKa, twenty orders of magnitude more basic than the corresponding acetylide. Arguably, this difference should result in a more electron-rich dinuclear core with new electronic structures waiting to be explored. Although kinetically more reactive than metal–alkynyls, metal–aryls are still more stable than the corresponding metal–alkyls. However, for second-row transition metals like ruthenium, kinetic instability issues are somewhat more suppressed than for their first-row counterparts.<br></div><div><br></div><div>Armed with the knowledge that it was reasonable to expect somewhat stable metal–aryl complexes, the synthesis and characterization, and analyses of molecular and electronic structures of diruthenium aryls were attempted. By employing relatively simple lithium-halogen exchange reactions, both mono and bis-aryl complexes of diruthenium have been isolated. Additionally, two different oxidation states of diruthenium have beenaccessed, namely Ru2(II,III)and Ru2(III,III),by judiciously modifying the paddlewheel ligands. Following this, preliminary reactivity studies of Ru2(II,III) monoaryls of the form Ru2(ap)4Ar were performed, which yielded surprising results. This work led to the conclusion that the diruthenium–aryl interaction is an example of a metal–metal–ligand interaction that can bring reactivity to the distal metal site. Moreover, it was found that even minor changes in axial ligands can bring about major upheavals in electronic structure.<br></div><div><br></div><div>Computational investigations into the electronic structure of the above-mentioned compounds have faced many a barrier because of the complexity of the system. The deep mixing of the metal–metal and metal–ligand valence manifolds is more easily isolated into its constituent parts in the case of relatively simple structures such as the monoaryls, Ru2II,IIIL4Ar. However, electronic structure calculations are fraught with difficulties in the case of heavily distorted axially disubstituted mono and bis-aryls, (X)Ru2III,IIIL4Ar and Ru2III,IIIL4Ar2, respectively. Ru2III,IIIL4Ar2complexes present an interesting case of second order Jahn-Teller distortion (SOJT), which has been adequately modeled. However, the more heavily distorted case of XRu2(ap)4Ar (X = CCH, CN, CO, etc.) pose greater computational challenges, such as low-lying excited states, spin-admixed ground states and difficulties in isolating metal and ligand contributions to the valence manifold. <br></div><div><br></div><div>Our investigations into diruthenium aryls began as a mere curiosity that arose out of a serendipitous discovery. Two years later, our continued efforts in this direction have yielded rather fruitful results. The unusual structures and associated complex bonding motifs in these systems have taught us about the importance of metal–metal–ligand interactions as more than just a sum of metal–metal and metal–ligand parts.<br></div>
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Formation and Decomposition of Platinum–Thallium Bond, Kinetics and Mechanism. Structural Characterization of Some Metal Cyanides in the Solid StateNagy, Péter January 2004 (has links)
The kinetic and mechanistic features of a new series ofplatinum-thallium cyano compounds containing a direct andunsupported by ligands metal-metal bond have been studied insolution, using standard mixandmeasurespectrophotometric technique and stoppedflow method.These reactions are interpreted as oxidative addition of the cspecies to the square planar Pt(CN)42-complex. Each of these processes was found to befirst-order in Pt(CN)42-, the corresponding TIIIIcomplex and a cyanide ion donating species whichacts as a catalyst. Both di- and trinuclear complexes werestudied, and the kinetically significant thallium complexes intheir formation and the catalytically active cyanide sourcesare as follows: [(CN)5PtTl(CN)3]3-: Tl(CN)4(alkaline region), Tl(CN)3(slightly acidic region) and CN; [(CN)5PtTl(CN)]: Tl(CN)2+and Tl(CN)2+; [(CN)5PtTlPt(CN)5]3-: [(CN)5PtTl(CN)]and HCN. Appropriatemechanisms were postulated for the overall reactions in allcases, which include i) metalmetal bond formation stepand ii) coordination of an axial cyanide ion to the platinumcenter. Two experimentally indistinguishable kinetic modelswere proposed for the formation of the dinuclear complexeswhich are different in the sequence of the two steps. In thecase of the trinuclear complex, experimental evidence isavailable to exclude one of the alternative reaction paths, andit was proven that the metalmetal bond formation precedesthe axial cyanide coordination. The cyanide ligands coordinated to TIIIIin the PtTl complexes could be replacedsuccessfully with aminopolycarboxylates e.g.: mimda2-, nta3-, edta4-. The [(CN)5PtTl(edta)]4-complex, with a direct metalmetal bond hasbeen prepared in solution by two different reactions: a)dissolution of [(CN)5PtTl](s) in an aqueous solution of edta, b)directly from Pt(CN)42-and Tl(edta)(CN)2-. The decomposition reaction is greatlyaccelerated by cyanide and significantly inhibited by edta. Itproceeds through the [(CN)5PtTl(CN)3]3-intermediate. The formation of [(CN)5PtTl(edta)]4-can proceed via two different pathways dependingon the ratio of the cyanide to the edta ligand concentrations.Thedirect pathat excess of edta means theformation of intermediate[(CN)4Pt···Tl(CN)(edta)]4-, followed by a release of the cyanide from theTlcentre followed by coordination of a cyanide from thebulk to the Ptcentre of the intermediate. Theindirect pathdominates in the absence of extraedta and the formation of the PtTl bond occours betweenPt(CN)42-and Tl(CN)4. Homoligand MTl(CN)4(M = TlI, K, Na) and, for the first time, Tl(CN)3species have been synthesized in the solid stateand their structures solved by single crystal Xraydiffraction method. Interesting redox processes have been foundbetween TIIIIand CNin nonaqueous solution and in Tl2O3-CNaqueous suspension. In the crystal structureof Tl(CN)3·H2O, the thallium(III) ion has a trigonal bypiramidalcoordination geometry with three cyanides in the trigonalplane, while an oxygen atom of the water molecule and anitrogen atom from a cyanide ligand attached to a neighboringthallium complex, form a linear OTlN fragment.Cyanide ligand bridges thallium units forming an infinitezigzag chain structure. Among the thallium(III) tetracyanocompounds, the isostructural M[Tl(CN)4](M = Tl and K) and Na[Tl(CN)4]·3H2O crystallize in different crystal systems, but thethallium(III) ion has in all cases the same tetrahedralgeometry in the [Tl(CN)4]unit. Three adducts of mercury(II) (isoelectronic with TIIII) (K2PtHg(CN)6·2H2O, Na2PdHg(CN)6·2H2O and K2NiHg(CN)6·2H2O) have been prepared from Hg(CN)2and square planar transition metal cyanides MII(CN)42-and their structure have been studied by singlecrystal Xray diffraction, XPS and Raman spectroscopy inthe solid state. The structure of (K2PtHg(CN)6·2H2O consists of strictly linear one dimensional wireswith PtIIand HgIIcenters located alternately, dHgPt= 3.460 Å. The structure of Na2PdHg(CN)6·2H2O and K2NiHg(CN)6·2H2O can be considered as double salts, the lack ofheterometallophilic interaction between both the HgIIand PdIIatoms, dHgPd= 4.92 Å, and HgIIand NiIIatoms, dNiPd= 4.60 Å, seems obvious. Electronbinding energy values of the metallic centers measured by XPSshow that there is no electron transfer between the metal ionsin all three adducts. In solution, experimental findingsclearly indicate the lack of metalmetal bond formation inall studied HgIICN-MII(CN)42-systems (M = Pt, Pd and Ni). It is in contrary tothe platinumthallium bonded cyanides. KEYWORDS:metalmetal bond, platinum, thallium,kinetics, mechanism, stopped flow, oxidative addition, cyanocomplexes, edta, redox reaction, metal cyanides, Xraydiffraction, Raman, NMR, mercury, palladium, nickel, onedimensional wire
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Compounds with Non-Buttressed Metal-Metal Bond between Platinum and Thallium. Model Systems for Photoinduced Two-Electron-Transfer.Maliarik, Mikhail January 2001 (has links)
A new family of oligonuclear cyano compounds incorporatingtransition (Pt) and main group (Tl) metals bound with anon-buttressed Pt-Tl bond was synthesised in aqueous solution.The metal-metal linkage is formed in the reaction betweenplatinum and thallium in their stable oxidation forms, Pt(II)and Tl(III), orvice versa: Pt(IV) and Tl(I). Four binuclear complexeswith a general composition [(CN)5Pt-Tl(CN)n(aq)]n-(n = 0-3) and a trinuclear species [(NC)5Pt-Tl-Pt(CN)5]3-were identified and structurally characterised insolution by multinuclear NMR, EXAFS and vibrationalspectroscopy. In aqueous solution the complexes exist inequilibrium. The distribution between the species can bealtered by varying the molar ratio Pt/Tl, cyanide concentrationand pH. Stability constants of the compounds weredetermined. A new compound (NC)5PtTl was also prepared in solid and its crystalstructure solved by a combination of X-ray powder diffractionand EXAFS. Altogether the values of195Pt-205Tl spin-spin coupling constants (25-71 kHz),interatomic Pt-Tl distances (2.598-2.638 Å), and vibrationstretching frequencies v (Pt-Tl) (159-164 cm-1) are fully indicative of a direct and unsupportedPt-Tl bond. The calculated values of Pt-Tl force constants(1.56-1.74 N· cm-1) are characteristic for single metal-metal bond.The oxidation status in the compounds can be viewed asintermediate between II and IV for platinum, and between I andIII for thallium, as reflected by the chemical shifts of195Pt and205Tl nuclei, C≡ N stretching frequencies andelectron binding energies. The compounds are capable to undergo a photoinducedtwo-electron transfer between the coupled hetero-metal ions.Upon irradiation into the metal-to-metal charge transferabsorption band, effective photoredox reaction takes place. Itresults in scission of the Pt-Tl bond and formation of variouscomplexes of oxidised platinum (Pt(III, IV)) and reducedthallium (Tl(I)). The values of photodecomposition quantumyields were determined from a stationary photolysis study ofthe heterometallic complexes. Nanosecond laser flash photolysisof the heteronuclear Pt-Tl cyano compounds was performed in thetimescale range 1· 10-6- 5· 10-2s and several intermediate species were detectedand characterised by optical spectroscopy. The heteronuclear Pt-Tl cyano compounds can be furthermodified in terms of their stability, solubility, and lightabsorption characteristics. It has been found that the platinumpentacyano unit of the [(NC)5Pt-Tl(CN)n(aq)]n-species is inert towards the tested ligands,whereas the thallium "part" of the complexes can be tunedsignificantly. A number of complexes [(NC)5Pt-Tl(L)m]x-(L-ligand) were prepared and characterised insolution. Compounds [(NC)5Pt-Tl(nta)(H2O)]3-, [(NC)5Pt-Tl(bipy)(DMSO)3], and [(NC)5Pt-Tl(bipy)2]have been prepared in solid and their structuresdetermined by single-crystal X-ray diffraction. <b>Keywords:</b>thallium, platinum, cyanide, metal-metal bond,non-buttressed, heterobimetallic, photoinduced, electrontransfer, redox reaction, NMR, chemical shift, spin-spincoupling constant, Raman, EXAFS, X-ray diffraction,equilibrium, oxidation state, oxidative addition,photolysis
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