Chiral Dinuclear EuIII , TbIII , and YIII Complexes Supported by P-Stereogenic Linear Tetraphosphine Tetraoxide.

A P-stereogenic linear tetraphosphine tetraoxide, (R,R)- or (S,S)-dpmppm(=O)4 , was synthesized to prepare C2 dinuclear M(hfa)3 complexes (M=Eu, Tb, Y) as the first example of lanthanide(III) complexes with P-chiral multidentate phosphine oxides. The mononuclear M(hfa)3 complexes (M=Eu, Y) with a P-chiral diphosphine dioxide, tpdpb(=O)2 , were also prepared, and comparison of their photophysical properties for the EuIII complexes revealed that significant chiral induction from the P-chiral centers arises on the achiral M(hfa)3 units through intramolecular π-π stacking constraint in the dinuclear system.

Unsymmetric Dinuclear RhI2 and RhIRhIII Complexes Supported by Tetraphosphine Ligands and Their Reactivity of Oxidative Protonation and Reductive Dechlorination.

Two linear tetradentate phosphine ligands, meso-Ph2PCH2P(Ph)CH2XCH2P(Ph)CH2PPh2 (X = CH2 (meso-dpmppp), NBn (meso-dpmppmNBn; Bn = benzyl)) were utilized to synthesize unsymmetrical dinuclear RhI complexes, [Rh2Cl2(meso-dpmppp)(L)] (L = XylNC (1a), CO (1b)) and [Rh2Cl2(meso-dpmppmNBn)(L)] (L = XylNC (1c), CO (1d)), where electron-deficient RhI → RhI centers with 30 valence electrons are supported by a tetraphosphine in an unusual cis-/trans-P,P coordination mode. The RhI dimers of 1a-d were treated with HCl under air to afford the RhI → RhIII dimers with 32 e-, [Rh2Cl4(meso-dpmppp)(L)] (L = XylNC (4a), CO (4b)) and [Rh2Cl4(meso-dpmppmNBn)(L)] (L = XylNC (4c), CO (4d)), via intermediate hydride complexes, [{RhCl2(µ-H)RhCl(L)}(meso-dpmppp)] (L = XylNC (2a), CO (2b)) and [{RhCl2(µ-H)RhCl(L)}(meso-dpmppmNBn)] (L = XylNC (2c), CO (2d)), and [{Rh(H)Cl2(µ-Cl)Rh(L)}(meso-dpmppp)] (L = XylNC (3a), CO (3b)) and [{Rh(H)Cl2(µ-Cl)Rh(L)}(meso-dpmppmNBn)] (L = XylNC (3c), CO (3d)). The hydride intermediates 2 and 3 were monitored under nitrogen by 1H{31P} and 31P{1H} NMR techniques to reveal two reaction pathways depending on the terminal auxiliary ligand L. Further, the reductive dechlorination converting RhIRhIII (4b,d) to RhI2 (1b,d) was accomplished with a CO terminal ligand by reacting with various amines that acted as one-electron reducing agents through an inner-sphere electron transfer mechanism. DFT calculations were performed to elucidate the electronic structures of 1a-d and 4a-d and to estimate the structures of the hydride intermediate complexes 2 and 3.

Octapalladium Strings Trap C60 and C70 Fullerenes Affording Metal-Chain-Wired Bucky Balls.

Reactions of Pd8 strings supported by meso-Ph2 PCH2 P(Ph)CH2 P(Ph)CH2 PPh2 (meso-dpmppm) ligands, [Pd8 (meso-dpmppm)4 (L)2 ]4+ (L=CH3 CN (1), XylNC (2)) with C60 resulted in the exclusive formation of unprecedented metal-chain-wired C60 bucky balls, [{Pd4 (meso-dpmppm)2 (L)}2 (C60 )]4+ (L=CH3 CN (11), XylNC (12)), in which a C60 fullerene is trapped in the central Pd-Pd junction, as unambiguously established by spectroscopic, X-ray crystallographic, and theoretical techniques. The similar reaction of Pd8 strings supported by rac-dpmppm, [Pd8 (rac-dpmppm)4 (CH3 CN)2 ]4+ (3) also afforded a racemic mixture of [{Pd4 ((R*,R*)-dpmppm)2 (CH3 CN)}2 (C60 )]4+ (13) without scrambling the Pd4 fragments with (R,R)- and (S,S)-dpmppm ligands. Consequently, those of enantiopure chiral Pd8 strings, [Pd8 ((R*,R*)-dpmppm)4 (CH3 CN)2 ]4+ , certainly afforded chiral bucky balls of [{Pd4 ((R*,R*)-dpmppm)2 (CH3 CN)}2 (C60 )]4+ (13RR and 13SS ), that exhibit mirror-image circular dichroism spectra. The reactions of 1 and 2 were also applied for trapping a C70 fullerene to give 2 : 1 adducts of [{Pd4 (meso-dpmppm)2 (L)}2 (C70 )]4+ (L=CH3 CN (21), XylNC (22)). These results provide useful information for creating a platform to develop dimensionally and chirality controlled metal-carbon nanocomposite materials.

Fine Tunable, Redox Active Octapalladium Chains Supported by Linear Tetraphosphines, Leading to Dynamically 1D Self-Assembled Coordination Polymers.

A series of the octapalladium chains supported by meso-Ph2 PCH2 P(Ph)CH2 P(Ph)CH2 PPh2 (meso-dpmppm) ligands, [Pd8 (meso-dpmppm)4 (L)2 ](BF4 )4 (L=none (1), solvents: CH3 CN (2 a), dmf (2 b), dmso (2 c), RN≡C: R=Xyl (3 a), Mes (3 b), Dip (3 c), t Bu (3 d), Cy (3 e), CH3 (CH2 )7 (3 f), CH3 (CH2 )11 (3 g), CH3 (CH2 )17 (3 h)) and [Pd8 (meso-dpmppm)4 (X)2 ](BF4 )2 (X=Cl (4 a), N3 (4 b), CN (4 c), SCN (4 d)), were synthesized by using 2 a as a stable good precursor, and characterized by spectroscopic (IR, 1 H and 31 P NMR, UV-vis-NIR, ESI-MS) measurements and X-ray crystallographic analyses (for 1, 2 a, b, 3 a, b, e, f, 4 a-d). On the basis of DFT calculations on the X-ray determined structure of 2 b ([2b-Pd8 ]4+ ) and the optimized models [Pd8 (meso-Ph2 PCH2 P(H)CH2 P(H)CH2 PH2 )4 (CH3 CN)2 ]4+ ([Pd8 Ph8 ]4+ ) and [Pd8 (meso-H2 PCH2 P(H)CH2 P(H)CH2 PH2 )4 (CH3 CN)2 ]4+ ([Pd8 H8 ]4+ ), with and without empirically calculating dispersion force stabilization energy (B3LYP-D3, B3LYP), the formation energy between the two Pd4 fragments is assumed to involve mainly noncovalent interactions (ca. -70 kcal/mol) with four sets of interligand C-H/π interactions and Pd⋅⋅⋅Pd metallophilic one, while electron shared covalent interactions are almost canceled out within the Pd8 chain. All the compounds isolated are stable in solution and exhibit characteristic absorption at ∼900 nm, which is assignable to a spin allowed HOMO to LUMO transition, and shows temperature dependent intensity change with variable absorption coefficients presumably due to coupling with some thermal vibrations. The structures and electronic states of the Pd8 chains are found finely tunable by varying the terminal capping ligands. In particular, theoretical calculations elucidated that the HOMO-LUMO energy gap is systematically related to the central Pd-Pd distance (2.7319(6)-2.7575(6) Å) by two ways with neutral ligands L (1, 2, 3) and with anionic ligands X (4), which are reflected on the NIR absorption energy of 867-954 nm. The isocyanide terminated Pd8 complexes (3) further reacted with excess of RNC (6 eq) to afford the Pd4 complexes, [Pd4 (meso-dpmppm)2 (RNC)2 ](BF4 )2 (13), and the cyclic voltammograms of 2 a (L=CH3 CN), 3, and 13 (R=Xyl, Mes, t Bu, Cy) demonstrated wide range redox behaviors from 2{Pd4 }4+ to 2{Pd4 }0 through 2{Pd4 }2+ ↔{Pd8 }4+ , {Pd8 }3+ , and {Pd8 }2+ strings. The oxidized complexes, [Pd4 (meso-dpmppm)2 (RNC)3 ](BF4 )4 (16), were characterized by X-ray analyses, and the two-electron reduced chain of [Pd8 (meso-dpmppm)4 ](BF4 )2 (7) was analyzed by spectroscopic and electrochemical techniques and DFT calculations. Reactions of 2 a with 1 equiv. of aromatic linear bisisocyanide (BI) in CH2 Cl2 deposited insoluble coordination polymers, {[Pd8 (meso-dpmppm)4 (BI)](BF4 )4 }n (5), and interestingly, they were soluble in acetonitrile, 31 P{1 H} and 1 H DOSY NMR spectra as well as SAXS curves suggesting that the coordination polymers may exist in acetonitrile as dynamically 1D self-assembled coordination polymers comprising ca. 50 units of the Pd8 rod averaged within the timescale.

Chiral Octapalladium Chains Supported by Enantiopure P-Stereogenic Linear Tetraphosphines, (R,R)- and (S,S)-Ph2PCH2P(Ph)CH2P(Ph)CH2PPh2.

Binuclear Pd(II) and Pt(II) complexes supported by rac-dpmppm (bis[(diphenylphosphinomethyl)phenylphosphino]methane) in a triply-bridged Z-form, [M2Cl4(rac-dpmppm)] (M = Pd (3a), Pt (3b)), readily reacted with 2,6-xylyl isocyanide (XylNC) in the presence of NH4PF6 to afford [M2Cl2(rac-dpmppm)(XylNC)2](PF6)2 (M = Pd (4a), Pt (4b)), in which each metal center accommodates one isocyanide ligand at the trans position to the inner P atom of dpmppm. Similarly, treatment of 3a and 3b with axially chiral (R/S)-1,1'-binaphthyl-2,2'-bisisocyanide (rac-Binac) in the presence of NH4OTf gave cyclic tetranuclear complexes, [{M2Cl2(rac-dpmppm)(rac-Binac)}2](OTf)4 (M = Pd (5), Pt (8)), where two {M2Cl2(rac-dpmppm)}2+ fragments are connected by two rac-Binac ligands through chirality sorting of (R*,R*)-dpmppm and (R*)-Binac. Complex 5 could be transformed into the halide exchanged tetranuclear complexes, [{Pd2X2(rac-dpmppm)(rac-Binac)}2](OTf)4 (X = Br (6), I (7)), to show that the rectangular arrangement of four Pd(II) ions is elongated by repulsive interaction between halide ligands. By using (R)- and (S)-Binac, enantiopure Pd4 complexes, [{Pd2Cl2((R*,R*)-dpmppm)((R*)-Binac)}2](OTf)4 (5RR/R and 5SS/S), were successfully isolated as pure crystalline forms, from which enantiopure (R,R)- and (S,S)-dpmppm were obtained by treatment with NaCN aqueous solution. Namely, optical resolution of rac-dpmppm was established through the tetranuclear Pd complexes, which is the first example for methylene-bridged polyphosphines, R2P(CH2PR)nCH2PR2 (n > 0). Furthermore, chiral octapalladium chains, [Pd8((R*,R*)-dpmppm)4(N≡CCH3)2](BF4)4 (2RR and 2SS), were synthesized by reacting enantiopure P-chiral dpmppm with [Pd2(CH3CN)6](BF4)2 and [Pd2(dba)3]·C6H6 and were characterized by spectroscopic and X-ray crystallographic analyses, to determine the absolute configurational structures. The Pd8 chains are the longest enantiopure chiral single-metal-atom chains structurally characterized, thus far, and the electronic structures were examined on the basis of DFT calculations of 2RR.

Facially Dispersed Polyhydride Cu9 and Cu16 Clusters Comprising Apex-Truncated Supertetrahedral and Square-Face-Capped Cuboctahedral Copper Frameworks.

By using a linear tetraphosphine, meso-bis[(diphenylphosphinomethyl)phenylphosphino]methane (dpmppm), nona- and hexadecanuclear copper hydride clusters, [Cu9 H7 (µ-dpmppm)3 ]X2 (X=Cl (1 a), Br (1 b), I (1 c), PF6 (1 d)) and [Cu16 H14 (µ-dpmppm)4 ]X2 (X2 =I2 (2 c), (4/3) PF6 ⋅(2/3) OH (2 d)) were synthesized and characterized. They form copper-hydride cages of apex-truncated supertetrahedral {Cu9 H7 }2+ and square-face-capped cuboctahedral {Cu16 H14 }2+ structures. The hydride positions were estimated by DFT calculations to be facially dispersed around the copper frameworks. A kinetically controlled synthesis gave an unsymmetrical Cu8 H6 cluster, [Cu8 H6 (µ-dpmppm)3 ]2+ (3), which readily reacted with CO2 to afford linear Cu4 complexes with formate bridges, leading to an unprecedented hydrogenation of CO2 into formate catalyzed by {Cu4 (µ-dpmppm)2 } platform. The results demonstrate that new motifs of copper hydride clusters could be established by the tetraphosphine ligands, and the structures influence their reactivity.

Synergistic Cu2 Catalysts for Formic Acid Dehydrogenation.

Hexanuclear copper hydride complexes, [Cu6(µ3-H)2( meso-L4)3(RNC)4](PF6)4 (R = tBu (6a), Cy (6b)), were prepared by using a new linear tetraphosphine, meso-Ph2PCH2P(Ph)(CH2)4P(Ph)CH2PPh2 ( meso-L4), and were converted into active catalysts of [Cu2(µ-O2CH)( meso-L4)(RNC)2]+ under the reaction conditions of formic acid dehydrogenation, where unsymmetric dinuclear copper sites supported by the tetradentate phosphine and isocyanide ligands were essential to demonstrate effective catalytic activity.

Alloyed Tetranuclear Metal Chains of Pd4-n Ptn (n=0-3) Scaffolded by a New Linear Tetraphosphine Containing a PNP Bridge.

A new linear tetraphosphine containing a PNP phosphazane bridge, rac-bis[(diphenylphosphinomethyl)phenylphosphino]phenylamine (rac-dpmppan), was synthesized and utilized to support a series of Pd/Pt mixed metal tetranuclear chains, [Pd4-n Ptn (µ-rac-dpmppan)2 (XylNC)2 ](PF6 )2 (XylNC=xylyl isocyanide; n=0: Pd4 (1), 1: PtPd3 (2), 2: PtPd2 Pt (3), 2: Pt2 Pd2 (4), 3: Pt2 PdPt (5)), in which the number and positions of additional Pt atoms were successfully controlled depending on the respective synthetic procedures using transformations from 1 to 3 through 2 and from 4 to 5 by redox-coupled exchange reactions. The 31 P{1 H} NMR and ESI mass spectra and X-ray diffraction analyses revealed almost identical tetranuclear structures, with slight contraction of metal-metal bonds according to incorporation of Pt atoms. The electronic absorption spectra of 1-5 exhibited characteristic bands at 635-510 nm with an energy propensity depending on the number and positions of Pt centres, which were assigned to HOMO (dσ*σσ*) to LUMO (dσ*σ*σ*) transition by theoretical calculations. The present results demonstrated that the electronic structures of Pd/Pt mixed-metal tetranuclear complexes are finely tuned as orbital-overlapping alloyed metal chains by atomically precise Pt incorporation in the Pd4 chain.

Tri- and Tetranuclear Copper Hydride Complexes Supported by Tetradentate Phosphine Ligands.

Three types of tetradentate phosphine ligands with different central methylene chains and configurations, meso- and rac-Ph2PCH2P(Ph)(CH2) nP(Ph)CH2PPh2 ( n = 2, meso- and rac-dpmppe; n = 3, meso-dpmppp) were utilized to synthesize a new series of tri- and tetranuclear copper hydride complexes. Reactions of meso-dpmppe or meso-dpmppp with CuCl/NH4PF6 or [Cu(CH3CN)4]PF6 in the presence of NaBH4 afforded trinuclear copper hydride complexes, [Cu3(µ3-H)( meso-dpmppe)2](PF6)2 (1) and [Cu3(µ3-H)( meso-dpmppp)2](PF6)2 (2), while a similar reaction with rac-dpmppe resulted in the formation of a tetranuclear copper dihydride complex, [Cu4(µ3-H)2( rac-dpmppe)2](PF6)2 (5). Complexes 1 and 5 further reacted with RNC (R = tBu, Cy, Xyl) to give [Cu3(µ3-H)( meso-dpmppe)2(XylNC)](PF6)2 (3), [Cu4(µ3-H)2( meso-dpmppe)2(RNC)2](PF6)2 (R = tBu (4a), Cy (4b)) and [Cu4(µ3-H)2( rac-dpmppe)2(RNC)2](PF6)2 (R = tBu (6a), Cy (6b), Xyl (6c)), respectively. Complexes 1-6 were characterized by ESI-MS and 1H and 31P NMR spectroscopy and X-ray diffraction analyses, demonstrating that a hydride ligand is located at the center of triangular Cu3 plane of 1-3, while two µ3-hydride-capped Cu3 planes are fused to result in rhombic Cu4H2 structures in 4a,b, 5, and 6a-c. Complexes 1-6 in CD3CN solutions notably showed high thermal stability and no reactivity toward H2O and CO2. DFT calculations indicated an interesting correlation between the Wiberg bond indices (WBI) of Cu-H bonds and their natural atomic charge (NAC), where the isocyanide ligands had an appreciable influence on the Cu-H interactions.

A Fluxional Cu8 H6 Cluster Supported by Bis(diphenylphosphino)methane and its Facile Reaction with CO2.

A copper hydride cluster [Cu8 (µ-H)6 (µ-dppm)5 ](PF6 )2 (dppm=bis(diphenylphosphino)methane) was prepared from reaction of [CuH(PPh3 )]6 with dppm in the presence of [Cu(CH3 CN)4 ]PF6 and exhibited fluxional behaviors in solution where the hydrides and the phosphines are scrambling around the trans-bicapped octahedral Cu8 framework. The Cu8 H6 complex showed facile reactivity with CO2 (1 atm, RT) to afford a tricopper complex, [Cu3 (µ-H)(µ-O2 CH)(µ-dppm)3 ]PF6 , which could be developed to unprecedented hydrosilylation of CO2 catalyzed by multinuclear CuH species under mild conditions.

Planar PtPd3 Complexes Stabilized by Three Bridging Silylene Ligands.

A heterobimetallic PtPd3 complex supported by three bridging diphenylsilylene ligands, [Pt{Pd(dmpe)}3 (µ3 -SiPh2 )3 ] (1, dmpe=1,2-bis(dimethylphosphino)ethane), has been synthesized from mononuclear Pd and Pt complexes. The hexagonal core composed of Pt, Pd, and Si atoms is slightly larger than that of the tetrapalladium complex, [Pd{Pd(dmpe)}3 (µ3 -SiPh2 )3 ] (2). Reaction of PhSiH3 with complex 1 in the presence and absence of Ph2 SiH2 results in the formation of a tetranuclear complex with silyl and hydride ligands at the Pt center, [PtH(SiPh2 H){Pd(dmpe)}3 (µ3 -SiHPh)3 ] (3), and an octanuclear complex, [{Pt{Pd(dmpe)}3 (µ3 -SiHPh)3 }2 (κ2 -dmpe)] (5), respectively. Both M-Si (M=Pt, Pd) bond lengths and the 29 Si NMR chemical shifts of 1 and 2 are located between those of mononuclear late transition-metal complexes with a silylene ligand and complexes with donor-stabilized silylene ligands. CuI and AgI adducts of 1 and 2, formulated as [M(µ-M'I){Pd(dmpe)}3 (µ3 -SiPh2 )3 ] (M=Pt, Pd; M'=Cu, Ag), undergo elimination of CuI (AgI) and regenerate the tetrametallic complexes upon heating or addition of a chelating diphosphine. Elimination of AgI from 2-AgI occurs more rapidly than elimination of CuI from 2-CuI, as determined from the results of kinetics experiments.

Chiral Self-Recognition between Stereogenic Tetrapalladium Units Affording Pd8 Chains Supported by Homochiral Tetraphosphines.

By using a chiral tetraphosphine, rac-bis[(diphenylphosphinomethyl)phenylphosphino]methane (rac-dpmppm), linear octapalladium chains were synthesized as discrete molecules of [Pd8 (µ-rac-dpmppm)4 L2 ](BF4 )4 (L=CH3 CN, dmf, XylNC), [Pd8 (µ-rac-dpmppm)4 ](BF4 )4 , and [Pd8 (µ-rac-dpmppm)4 (Cl)2 ](BF4 )2 , which are stable in the solution states and characterized by spectroscopic and crystallographic methods to reveal the octapalladium chains supported by homochiral four tetraphosphines. Variable-temperature NMR studies for a 1:1 mixture of [Pd8 (µ-rac-dpmppm)4 (dmf)2 ](BF4 )4 and [Pd8 (µ-meso-dpmppm)4 (dmf)2 ]-(BF4 )4 in [D7 ]DMF revealed that the Pd8 chains were dissociated at higher temperature (T≈140 °C) into the Pd4 units of {Pd4 (µ-rac-dpmppm)2 }2+ and {Pd4 (µ-meso-dpmppm)2 }2+ , and they were thermodynamically self-aligned to restore the Pd8 chains at lower temperature (T<60 °C), through perfect chiral self-recognition between the stereogenic tetrapalladium units.

Stepwise Expansion of Pd Chains from Binuclear Palladium(I) Complexes Supported by Tetraphosphine Ligands.

Reaction of [Pd2(XylNC)6]X2 (X = PF6, BF4) with a linear tetraphosphine, meso-bis[(diphenylphosphinomethyl)phenylphosphino]methane (dpmppm), afforded binuclear Pd(I) complexes, [Pd2(µ-dpmppm)2]X2 ([2]X2), through an asymmetric dipalladium complex, [Pd2(µ-dpmppm)(XylNC)3](2+) ([1](2+)). Complex [2](2+) readily reacted with [Pd(0)(dba)2] (2 equiv) and an excess of isocyanide, RNC (R = 2,6-xylyl (Xyl), tert-butyl ((t)Bu)), to generate an equilibrium mixture of [Pd4(µ-dpmppm)2(RNC)2](2+) ([3'](2+)) + RNC ⇄ [Pd4(µ-dpmppm)2(RNC)3](2+) ([3](2+)), from which [Pd4(µ-dpmppm)2(XylNC)3](2+) ([3a](2+)) and [Pd4(µ-dpmppm)2((t)BuNC)2](2+) ([3b'](2+)) were isolated. Variable-temperature UV-vis and (31)P{(1)H} and (1)H NMR spectroscopic studies on the equilibrium mixtures demonstrated that the tetrapalladium complexes are quite fluxional in the solution state: the symmetric Pd4 complex [3b'](2+) predominantly existed at higher temperatures (>0 °C), and the equilibrium shifted to the asymmetric Pd4 complex [3b](2+) at a low temperature (∼-30 °C). The binding constants were determined by UV-vis titration at 20 °C and revealed that XylNC is of higher affinity to the Pd4 core than (t)BuNC. In addition, both isocyanides exhibited higher affinity to the electron deficient [Pd4(µ-dpmppmF2)2(RNC)2](2+) ([3F'](2+)) than to [Pd4(µ-dpmppm)2(RNC)2](2+) ([3'](2+)) (dpmppmF2 = meso-bis[{di(3,5-difluorophenyl)phosphinomethyl}phenylphosphino]methane). When [2]X2 was treated with [Pd(0)(dba)2] (2 equiv) in the absence of RNC in acetonitrile, linearly ordered octapalladium chains, [Pd8(µ-dpmppm)4(CH3CN)2]X4 ([4]X4: X = PF6, BF4), were generated through a coupling of two {Pd4(µ-dpmppm)2}(2+) fragments. Complex [2](2+) was also proven to be a good precursor for Pd2M2 mixed-metal complexes, yielding [Pd2Cl(Cp*MCl) (Cp*MCl2)(µ-dpmppm)2](2+) (M = Rh ([5](2+)), Ir ([6](2+)), and [Au2Pd2Cl2(dpmppm-H)2](2+) ([7](2+)) by treatment with [Cp*MCl2]2 and [AuCl(PPh3)], respectively. Complex [7](2+) contains an unprecedented PC(sp(3))P pincer ligand with a PCPCPCP backbone, dpmppm-H of deprotonated dpmppm. The present results demonstrated that the binuclear Pd(I) complex [2](2+) was a quite useful starting material to extend the palladium chains and to construct Pd-involved heteromultinuclear systems.

Self-alignment of low-valent octanuclear palladium atoms.

A linear tetraphosphine, meso-bis[(diphenylphosphinomethyl)phenylphosphino]methane (dpmppm) was used to synthesize linear octapalladium-extended metal atom chains as discrete molecules of [Pd8(µ-dpmppm)4](BF4)4 (1) and [Pd8(µ-dpmppm)4L2](BF4)4 (L=2,6-xylyl isocyanide (XylNC; 2), acetonitrile (3), and N,N-dimethylformamide (dmf; 4)), which are stable in the solution states and show interesting temperature-dependent photochemical properties in the near IR region. Variable temperature NMR studies demonstrated that at higher temperature T≈140 °C the Pd8 chains were dissociated into Pd4 fragments, which were thermodynamically self-aligned to restore the Pd8 chains at lower temperature T<60 °C. The coldspray ionization mass spectra suggested a possibility for further aggregation of the linear tetrapalladium units.

Strongly luminous tetranuclear gold(I) complexes supported by tetraphosphine ligands, meso- or rac-bis[(diphenylphosphinomethyl)phenylphosphino]methane.

A series of tetragold(I) complexes supported by tetraphosphine ligands, meso- and rac-bis[(diphenylphosphinomethyl)phenylphosphino]methane (meso- and rac-dpmppm) were synthesized and characterized to show that the tetranuclear Au(I) alignment varies depending on syn- and anti-arrangements of the two dpmppm ligands with respect to the metal chain. The structures of syn-[Au4 (meso-dpmppm)2X]X'3 (X = Cl; X' = Cl (4 a), PF6 (4 b), BF4 (4 c)) and syn-[Au4 (meso-dpmppm)2]X4 (X = PF6 (4 d), BF4 (4 e), TfO (4 f); TfO = triflate) involved a bent tetragold(I) core with a counter anion X incorporated into the bent pocket. Complexes anti-[Au4 (meso-dpmppm)2]X4 (X = PF6 (5 d), BF4 (5 e), TfO (5 f)) contain a linearly ordered Au4 string and complexes syn-[Au4 (rac-dpmppm)2X2]X'2 (X = Cl, X' = Cl (6 a), PF6 (6 b), BF4 (6 c)) and syn-[Au4 (rac-dpmppm)2]X4 (X = PF6 (6 d), BF4 (6 e), TfO (6 f)) consist of a zigzag tetragold(I) chain supported by the two syn-arranged rac-dpmppm ligands. Complexes 4 d-f, 5 d-f, and 6 d-f with non-coordinative large anions are strongly luminescent in the solid state (λmax = 475-515 nm, Φ = 0.67-0.85) and in acetonitrile (λmax = 491-520 nm, Φ = 0.33-0.97); the emission was assigned to phosphorescence from (3) [dσ*σ*σ* pσσσ] excited state of the Au4 centers on the basis of DFT calculations as well as the long lifetime (a few µs). The emission energy is predominantly determined by the HOMO and LUMO characters of the Au4 centers, which depend on the bent (4), linear (5), and zigzag (6) alignments. The strong emissions in acetonitrile were quenched by chloride anions through simultaneous dynamic and static quenching processes, in which static binding of chloride ions to the Au4 excited species should be the most effective. The present study demonstrates that the structures of linear tetranuclear gold(I) chains can be modified by utilizing the stereoisomeric tetraphosphines, meso- and rac-dpmppm, which may lead to fine tuning of the strongly luminescent properties intrinsic to the Au(I) 4 cluster centers.

Aiming for dynamic behaviours of molecular metal chains.

The dynamical functions of molecular metal chains, that could be derived from unique physical and chemical properties coupled with self-assembly of metal chain components, have largely been unexplored, and this review paper focuses on the dynamic behaviours of Pd chains supported by linear tetraphosphines, meso- and rac-Ph2PCH2P(Ph)CH2P(Ph)CH2PPh2 recently reported, and the current development on fine-tuning of metal chains by introducing heterometal atoms, i.e. heterometallic molecular metal chains, that are considered as promising dynamical components in the next generation.

Wheel-shaped icosanuclear homo- and heterometallic complexes of Ni(II), Co(II), and Cu(II) ions supported by unsymmetrical aminoalcohol ligands.

Reactions of M(OAc)2·4H2O (M = Ni, Co) with 3-[benzyl(2-hydroxyethyl)amino]-1-propanol (H2L) in the presence of pyridine or triethylamine afforded novel homometallic icosanuclear wheel-shaped complexes [M20L4(HL)4(OAc)28] (M = Ni (1), Co (2)), which consist of a central M(II)12 single-stranded, nearly planar loop with four peripheral [M2(HL)(OAc)2] fragments attached in an S4 symmetrical fashion. The complexes can alternatively be recognized as saddle-shaped wheel structures, in which four tetranuclear units of [M4L(HL)(OAc)7](2-) are connected by four M(2+) ions (M5). The tetranuclear unit itself can be derived from an ideal C2 symmetrical [M4(HL)2(µ-η(2)-OAc)4(µ-η(1),η(1)-OAc)2(η(1),η(1)-OAc)](-) structure through deprotonation of the HL(-) ligand, and is composed of two plane-shared M3O4 incomplete cubanes in which the M2 and M3 atoms are involved in the central fused plane and the M1 and M4 atoms are disposed at the apex sites. Mixed-metal icosanuclear complexes [NixM20-xL4(HL)4(OAc)28] (3, M = Co, x = 9.5) and [Ni12M8L4(HL)4(OAc)28] (4, M = Cu) were also synthesized by using equimolar amounts of Ni(II) and M(II) ions, and were shown to have similar structures to 1 and 2. X-ray crystallographic and fluorescent analyses revealed that complex 3 contains nonstoichiometric amounts of Ni(2+) and Co(2+) ions in the ratio of 9.5:10.5 and that these are disordered at every metal site. In striking contrast, complex 4 has a stoichiometric formula of Ni12Cu8, which was confirmed by the Jahn-Teller elongation of Cu(2+) ions, and consequently, the M2 and M5 positions are occupied exclusively by the Cu(2+) ions. The temperature-dependent direct current (dc) magnetic susceptibility data showed the presence of ferromagnetic exchange interactions in the Ni homometallic (1) and NiCu bimetallic (4) complexes, while the Co homometallic (2) and NiCo bimetallic (3) complexes exhibited antiferromagnetic interactions due to spin-orbit coupling effects of the octahedral Co(II) ions. The present results demonstrate that the unsymmetrical aminoalcohol ligand H2L is quite effective in organizing the homo- and heterometallic icosanuclear wheel-shaped metal arrangements.

Tetrapalladium complex with bridging germylene ligands. Structural change of the planar Pd4Ge3 core.

A complex with a planar hexagonal Pd(4)Ge(3) core, [Pd{Pd(dmpe)}(3)(µ(3)-GePh(2))(3)], was synthesized and characterized by X-ray and NMR measurements as well as by DFT calculations. 4-tert-Butylbenzenethiol converted the Pd(4) complex into a hexapalladium complex, [{Pd(3)(µ-GePh(2))(2)(µ-H)(µ(3)-GePh(2)(SC(6)H(4)(t)Bu-4))}(2)(µ-dmpe)], composed of two Pd(3)Ge(3) units bridged by a dmpe ligand. The addition of CuI or AgI to the Pd(4) complex yielded [Pd(µ-MI){Pd(dmpe)}(3)(µ(3)-GePh(2))(3) ] (M = Cu, Ag), in which Cu or Ag bridges a Pd-Pd bond of the Pd(4)Ge(3) core. The CuI adducts in solution undergo a pivot motion of the CuI on the surface of the Pd(4)Ge(3) plane on the NMR time scale.

Electrochemical hydrogen formation catalysed by a Pd8 string.

The linear Pd8 complex supported by tetraphosphines reacted with HBF4 to give an unprecedented linear tetrapalladium complex with a terminal hydride, which promoted electrocatalytic hydrogen formation from HBF4 in acetonitrile. The 1D coordination polymer of Pd8 chain confined within Nafion film was applied to the electrocatalytic H2 formation.

Chemically modified electrode with a film of nano ruthenium oxides stabilizing high valent RuO(4)(-) species and its redox-selective sequential transformation to polynuclear ruthenium oxide-metallocyanates.

High-valent Ru(VII)O(4)(-) (perruthenate) is a short-lived species in aqueous solutions (pH 1-14) and has scarcely been studied through electrochemistry. By a potential-controlled oxidative deposition method at 1 V vs Ag/AgCl using RuCl(3) in a pH 2 KCl-HCl buffer solution, chemically modified glassy carbon (GCE) and indium tin oxide (ITO) electrodes were successfully prepared with a film of hydrous nano ruthenium oxides RuO(2) and RuO(3), stabilizing the high-valent perruthenate anion (Ru(VII)-RuO(x)-CME, x = 2 and 3, CME = chemically modified electrode). The electrodes showed three distinct redox peaks corresponding to Ru(2)O(3)/RuO(2), RuO(2)/RuO(3), and RuO(4)(2-)/RuO(4)(-) redox processes at pH 2, like the classical RuO(2) electrodes in alkaline conditions. Solid state UV-visible spectra of the ITO/Ru(VII)-RuO(x)-CME showed characteristic absorption very close to chemically generated authentic RuO(4)(-) species in alkaline solution. Further, redox-controlled sequential procedures yielded polynuclear ruthenium oxide-hexacyanometallate films (RuO-MCN-CME, M = Fe and Ru), in which Ru(VII)-RuO(x)-CME acted as a specific template. A controlled-potential activation (>1 V) of Ru(VII)-RuO(x)-CME, stabilizing the key RuO(4)(-) species, in a solution of [Fe(CN)(6)](3-) or [Ru(CN)(6)](4-), should be a critical step for the formation of polynuclear RuO-MCN matrix.