A one-pot reduction route to bimetallic manganese 1,8-naphthyridine complexes.

Reaction of the dinucleating ligand 2,7-bis(6-methyl-2-pyridyl)-1,8-naphthyridine (MeL) with the MnI and MnII precursors MnBr(CO)5 and MnCl2 resulted in the formation of the monometallic complexes [MnBr(CO)3(MeL)] (1) and [MnCl2(MeL)] (3). In both cases, formation of bimetallic manganese complexes could be achieved by reduction with KC8, yielding the carbonyl-bridged complex [Mn2(CO)6(MeL)] (2) and the helicate complex [Mn2(MeL)2] (4), respectively. EPR results demonstrate that 4 represents a novel, weakly antiferromagnetically coupled homovalent dimer (J = -0.85 cm-1). The two formally Mn0 ions are both high spin (S = 3/2) and exhibit a zero-field splitting of ≈1 cm-1, suggesting reduction of the complex is substantially ligand centered, and may be better described as a MnII complex coupled to two open shell singlet ligands [MnII2(MeL2-)2]. X-ray crystallography, UV-Vis spectroscopy and DFT analysis support this finding.

Utilising a Proton-Responsive 1,8-Naphthyridine Ligand for the Synthesis of Bimetallic Palladium and Platinum Complexes.

We present four proton-responsive palladium and platinum complexes, [MCl2 (R PONNHO)] (M=Pd, Pt; R=i Pr, t Bu) synthesised by complexation of PdCl2 or PtCl2 (COD) with the 1,8-naphthyridine ligand R PONNHO. Deprotonation of [MCl2 (tBu PONNHO)] switches ligand coordination from mono- to dinucleating, offering a synthetic pathway to bimetallic PdII and PtII complexes [M2 Cl2 (tBu PONNO)2 ]. Two-electron reduction gives planar MI -MI complexes [M2 (tBu PONNO)2 ] (M=Pd, Pt) containing a metal-metal bond. In contrast to the related nickel system that forms a metallophosphorane [Ni2 (tBu PONNOPONNO)], an unusual phosphinite binding mode is observed in [M2 (tBu PONNO)2 ] containing close phosphinite-naphthyridinone P⋅⋅⋅O interactions, which is investigated spectroscopically, crystallographically and computationally. The presented proton-responsive and structurally-responsive R PONNHO and bimetallic R PONNO complexes offer a novel platform for future explorations of metal-ligand and metal-metal cooperativity with palladium and platinum.

Oxidative Addition and ß-Hydride Elimination by a Macrocyclic Dinickel Complex: Observing Bimetallic Elementary Reactions.

The dinickel(I) complex Ni2 (tBu PONNOPONNO), featuring a planar macrocyclic diphosphoranide ligand tBu PONNOPONNO, offers a unique architectural platform for observing bimetallic elementary reactions. Oxidative addition reactions of alkyl halides produce dinickel(II) complexes of the type Ni2 (µ-R)(µ-X)(tBu PONNOPONNO). However, when R=Et ß-hydride elimination is observed to form a dinickel monohydride, with the rate dependent on the nature of X. DFT studies suggest a new mechanism for bimetallic ß-hydride elimination, where the rate dependence arises from the steric pressure imposed by the X group on the opposing trans face of the dinickel macrocycle. This work enhances understanding of bimetallic elementary reactions, particularly ß-hydride elimination, which have not been well-explored for dinuclear systems.

Highly Adaptive Nature of Group 15 Tris(quinolyl) Ligands─Studies with Coinage Metals.

The substitution of heavier, more metallic atoms into classical organic ligand frameworks provides an important strategy for tuning ligand properties, such as ligand bite and donor character, and is the basis for the emerging area of main-group supramolecular chemistry. In this paper, we explore two new ligands [E(2-Me-8-qy)3] [E = Sb (1), Bi (2); qy = quinolyl], allowing a fundamental comparison of their coordination behavior with classical tris(2-pyridyl) ligands of the type [E'(2-py)3] (E = a range of bridgehead atoms and groups, py = pyridyl). A range of new coordination modes to Cu+, Ag+, and Au+ is seen for 1 and 2, in the absence of steric constraints at the bridgehead and with their more remote N-donor atoms. A particular feature is the adaptive nature of these new ligands, with the ability to adjust coordination mode in response to the hard-soft character of coordinated metal ions, influenced also by the character of the bridgehead atom (Sb or Bi). These features can be seen in a comparison between [Cu2{Sb(2-Me-8-qy)3}2](PF6)2 (1·CuPF6) and [Cu{Bi(2-Me-8-qy)3}](PF6) (2·CuPF6), the first containing a dimeric cation in which 1 adopts an unprecedented intramolecular N,N,Sb-coordination mode while in the second, 2 adopts an unusual N,N,(π-)C coordination mode. In contrast, the previously reported analogous ligands [E(6-Me-2-py)3] (E = Sb, Bi; 2-py = 2-pyridyl) show a tris-chelating mode in their complexes with CuPF6, which is typical for the extensive tris(2-pyridyl) family with a range of metals. The greater polarity of the Bi-C bond in 2 results in ligand transfer reactions with Au(I). Although this reactivity is not in itself unusual, the characterization of several products by single-crystal X-ray diffraction provides snapshots of the ligand transfer reaction involved, with one of the products (the bimetallic complex [(BiCl){ClAu2(2-Me-8-qy)3}] (8)) containing a Au2Bi core in which the shortest Au → Bi donor-acceptor bond to date is observed.

Bimetallic Nickel Complexes Supported by a Planar Macrocyclic Diphosphoranide Ligand.

Metal-metal cooperativity is emerging as an important strategy in catalysis. This requires appropriate ligand scaffolds that can support two metals in close proximity. Here we report nickel-promoted formation of a dinucleating planar macrocyclic ligand that can support bimetallic dinickel(II) and dinickel(I) complexes. Reaction outcomes can be tuned by variation of the substituents and reaction conditions to favour dinucleating macrocyclic, mononucleating macrocyclic or conventional pincer architectures.

Copper and Zinc Complexes of 2,7-Bis(6-methyl-2-pyridyl)-1,8-naphthyridine─A Redox-Active, Dinucleating Bis(bipyridine) Ligand.

The ligand 2,7-bis(6-methyl-2-pyridyl)-1,8-naphthyridine (MeL) acts as a dinucleating analogue of ubiquitous 2,2'-bipyridine ligands. Coordination of MeL to [Cu(NCMe)4]PF6 and Zn(OAc)2 led to isolation of monometallic [Zn(OAc)2(MeL)], homobimetallic [Cu2(MeL)2][PF6]2, and heterobimetallic [CuZn(µ-OAc)2(MeL)]PF6 complexes. The redox-active nature of the ligand enables access to four redox states of the complex [Cu2(MeL)2][PF6]2. DFT studies indicate that these comprise a metal-centered oxidative and ligand-centered reductive processes.

Cooperative approaches in catalytic hydrogenation and dehydrogenation.

Metal-ligand cooperativity (MLC) is an established strategy for developing effective hydrogenation and dehydrogenation catalysts. Metal-metal cooperativity (MMC) in bimetallic complexes is not as well understood, and to date has had limited implementation in (de)hydrogenation. Herein we use (de)hydrogenation processes as a platform to examine modes of cooperativity, with a particular focus on catalytic mechanisms. We investigate how lessons learnt from the extensive development of metal-ligand cooperative catalysts can aid the ongoing development of metal-metal cooperative catalysts.

Synthesis and coordination behaviour of aluminate-based quinolyl ligands.

The effects of moving the donor N-atom from the 2-position in lithium (2-pyridyl)- and (2-quinolyl)aluminates to the more remote position in (8-quinolyl)aluminates have been investigated by solid-state structural and DFT computational studies of the new complexes [{EtAl(2-qy)3}Li(µ-X)Li(THF)3] (X = Cl/Br 62 : 38) [(1)Li(µ-X)Li(THF)3], [{(EtAl(2-qy)3)Li}2(µ-Br)]-Li(THF)4+ [{1Li}2(µ-Br)]-Li(THF)4+, [{EtAl(2-Me-8-qy)3}Li] [(2)Li], [{Me2Al(2-Me-8-qy)2}Li(THF)] [(3a)Li(THF)], [{Me2Al(6-Me-2-py)2}Li(THF)2] [(4)Li(THF)2] and [{{EtAl(2-Me-8-qy)2}2O}(Li2THF)] (5). Increasing the remoteness of the donor N-atom from the bridgehead results in large differences in the coordination of the Li+ cations by the (8-quinolyl)aluminate anions compared to 2-quinolyl or 2-pyridyl counterparts. The results are of potential interest in understanding how the coordination sites of ligands of this type can be tuned for the coordination requirements of specific metal centres.

Synthesis of tris(3-pyridyl)aluminate ligand and its unexpected stability against hydrolysis: revealing cooperativity effects in heterobimetallic pyridyl aluminates.

We report the elusive metallic anion [EtAl(3-py)3]- (3-py = 3-pyridyl) (1), the first member of the anionic tris(3-pyridyl) family. Unexpectedly, the lithium complex 1Li shows substantial protic stability against water and alcohols, unlike related tris(2-pyridyl)aluminate analogues. This stability appears to be related to the inability of the [EtAl(3-py)3]- anion to chelate Li+, which precludes a decomposition pathway involving Li/Al cooperativity.

Synthesis of an expanded pincer ligand and its bimetallic coinage metal complexes.

An expanded pincer ligand tBu-PONNOP (2,7-bis(di-tert-butylphosphinito)-1,8-naphthyridine) has been synthesised and its coordination to coinage metals has been studied. Bimetallic complexes were produced with metal halide salts of the type [M2X2(tBu-PONNOP)] (X = Cl, M = Au, Ag, Cu; X = I, M = Cu) with a varying degree of interaction with the naphthyridyl backbone in the order Au < Ag < Cu. The salts [Ag2(tBu-PONNOP)2][BArF4]2 (ArF = 3,5-C6H3(CF3)2) and [Ag2(NCMe)2(tBu-PONNOP)]X2 (X = BArF4, PF6) were prepared, which may serve as a source of tBu-PONNOP via transmetallation.

Pnictogen-Functionalised C1 Ligands: MC-ARn (n=0, 1, 2, 3).

The chemistry of transition metal carbynes, Ln M≡CR, has historically been dominated by species bearing hydrocarbyl or amino 'R' substituents, with other elements appearing only sporadically. In recent years, carbynes and related 'C1 ' species bearing other main-group substituents, particularly heavier elements of the p-block, have begun to emerge. This review details the chemistry of heavier pnictogen-functionalised C1 ligands, MCARn (A=P, As, Sb, Bi; n=0-3), including their syntheses, properties and reactivities, and how these are distinguished from more traditional carbyne complexes. Recent developments in the closely related phospha-isonitrile Ln M(CPR), cya-phosphide and cya-arside ligands, Ln M(C≡A) (A=P, As), are also discussed.

An experimental and theoretical study of the coordination and donor properties of tris-2-pyridyl-phosphine ligands.

The coordination characteristics and donor/acceptor properties of a series of 2-pyridyl substituted phosphine ligands have been investigated using structural, spectroscopic and DFT calculational studies. A range of different coordination modes are observed in Mo and W carbonyl complexes of tris-2-pyridyl-phosphine ligands of the type P(2-py') (2-py' = substituted or unsubstituted 2-pyridyl group), including an unprecedented example exhibiting N,N',µ2-π coordination. DFT calculations were used to assess the relative donor/acceptor properties of a range of related 2-pyridyl-phosphine ligands with respect to PPh3 and PtBu3.

The role of neutral Rh(PONOP)H, free NMe2H, boronium and ammonium salts in the dehydrocoupling of dimethylamine-borane using the cationic pincer [Rh(PONOP)(η2-H2)]+ catalyst.

The σ-amine-borane pincer complex [Rh(PONOP)(η1-H3B·NMe3)][BArF4] [2, PONOP = κ3-NC5H3-2,6-(OPtBu2)2] is prepared by addition of H3B·NMe3 to the dihydrogen precursor [Rh(PONOP)(η2-H2)][BArF4], 1. In a similar way the related H3B·NMe2H complex [Rh(PONOP)(η1-H3B·NMe2H)][BArF4], 3, can be made in situ, but this undergoes dehydrocoupling to reform 1 and give the aminoborane dimer [H2BNMe2]2. NMR studies on this system reveal an intermediate neutral hydride forms, Rh(PONOP)H, 4, that has been prepared independently. 1 is a competent catalyst (2 mol%, ∼30 min) for the dehydrocoupling of H3B·Me2H. Kinetic, mechanistic and computational studies point to the role of NMe2H in both forming the neutral hydride, via deprotonation of a σ-amine-borane complex and formation of aminoborane, and closing the catalytic cycle by reprotonation of the hydride by the thus-formed dimethyl ammonium [NMe2H2]+. Competitive processes involving the generation of boronium [H2B(NMe2H)2]+ are also discussed, but shown to be higher in energy. Off-cycle adducts between [NMe2H2]+ or [H2B(NMe2H)2]+ and amine-boranes are also discussed that act to modify the kinetics of dehydrocoupling.

A Tris(3-pyridyl)stannane as a Building Block for Heterobimetallic Coordination Polymers and Supramolecular Cages.

The systematic assembly of supramolecular arrangements is a persistent challenge in modern coordination chemistry, especially where further aspects of complexity are concerned, as in the case of large molecular mixed-metal arrangements. One targeted approach to such heterometallic complexes is to engineer metal-based donor ligands of the correct geometry to build 3D arrangements upon coordination to other metals. This simple idea has, however, only rarely been applied to main group metal-based ligand systems. Here, we show that the new, bench-stable tris(3-pyridyl)stannane ligand PhSn(3-Py)3 (3-Py=3-pyridyl) provides simple access to a range of heterometallic SnIV /transition metal complexes, and that the presence of weakly coordinating counter anions can be used to build discrete molecular arrangements involving anion encapsulation. This work therefore provides a building strategy in this area, which parallels that of supramolecular transition metal chemistry.

Phosphaisonitrile umpolung - synthesis and reactivity of chloro aminophosphino carbynes.

Sequential treatment of [W([triple bond, length as m-dash]CBr)(CO)2(Tp*)] (Tp* = hydrotris(dimethylpyrazolyl)borate) with nBuLi and Cl2PNiPr2 provides the aminochlorophosphinocarbyne [W([triple bond, length as m-dash]CPClNiPr2)(CO)2(Tp*)]. The chloro substituent undergoes subsitution with RLi (R = Me, Et, Ph) to afford [W([triple bond, length as m-dash]CPRNiPr2)(CO)2(Tp*)] and with [W([triple bond, length as m-dash]CLi)(CO)2(Tp*)] to give the aminobis(alkylidynyl)phosphine [iPr2NP{C[triple bond, length as m-dash]W(CO)2(Tp*)}2]. Treatment with Li[BHEt3] gives the primary aminophosphine [W([triple bond, length as m-dash]CPHNiPr2)(CO)2(Tp*)], formed in a mixture with the ethyl derivative [W([triple bond, length as m-dash]CPEtNiPr2)(CO)2(Tp*)]. Although they could not be isolated, spectroscopic data indicated that halide abstraction with Al2Cl6 forms the phosphaisonitrile salt [W(CPNiPr2)(CO)2(Tp*)][AlCl4], which displays electrophilic character at phosphorus, e.g., in the reaction with diphenylacetylene to furnish the phosphirenium salt [W{CP(C2Ph2)NiPr2}(CO)2(Tp*)][AlCl4]. Finally, the reaction with LiNPh2 gives the mixed diaminophosphinocarbyne, [W{[triple bond, length as m-dash]CP(NiPr2)(NPh2)}(CO)2(Tp*)].

Deprotonation, insertion and isomerisation in the post-functionalisation of tris-pyridyl aluminates.

Post-functionalisation of the aluminate anion [EtAl(6-R-2-py)3]- (6-R-2-py = 6-R-2-pyridyl, R = Me or Br) can be accomplished via nucleophilic addition of the pyridyl groups to the electrophilic C[double bond, length as m-dash]O group of aldehydes (RCH[double bond, length as m-dash]O) or by deprotonation of carboxylic acids (RCO2H). NMR spectroscopic and crystallographic studies show how 6-Me-2-py groups can detect chirality and reveal a new aspect of isomerism.

Amine-Borane Dehydropolymerization: Challenges and Opportunities.

The dehydropolymerization of amine-boranes, exemplified as H2 RB⋅NR'H2 , to produce polyaminoboranes (HRBNR'H)n that are inorganic analogues of polyolefins with alternating main-chain B-N units, is an area with significant potential, stemming from both fundamental (mechanism, catalyst development, main-group hetero-cross-coupling) and technological (new polymeric materials) opportunities. This Concept article outlines recent advances in the field, covering catalyst development and performance, current mechanistic models, and alternative non-catalytic routes for polymer production. The substrate scope, polymer properties and applications of these exciting materials are also outlined. Challenges and opportunities in the field are suggested, as a way of providing focus for future investigations.

The coordination chemistry of the neutral tris-2-pyridyl silicon ligand [PhSi(6-Me-2-py)3].

Difficulties in the preparation of neutral ligands of the type [RSi(2-py)3] (where 2-py is an unfunctionalised 2-pyridyl ring unit) have thwarted efforts to expand the coordination chemistry of ligands of this type. However, simply switching the pyridyl substituents to 6-methyl-pyridyl groups (6-Me-2-py) in the current paper has allowed smooth, high-yielding access to the [PhSi(6-Me-2-py)3] ligand (1), and the first exploration of its coordination chemistry with transition metals. The synthesis, single-crystal X-ray structures and solution dynamics of the new complexes [{PhSi(6-Me-2-py)3}CuCH3CN][PF6], [{PhSi(6-Me-2-py)3}CuCH3CN][CuCl2], [{PhSi(6-Me-2-py)3}FeCl2], [{PhSi(6-Me-2-py)3}Mo(CO)3] and [{PhSi(6-Me-2-py)3}CoCl2] are reported. The paramagnetic Fe2+ and Co2+ complexes show strongly shifted NMR resonances for the coordinated pyridyl units due to large Fermi-contact shifts. However, magnetic anisotropy also leads to considerable pseudo-contact shifts so that both contributions have to be included in the paramagnetic NMR analysis.

How Changing the Bridgehead Can Affect the Properties of Tripodal Ligands.

Although a multitude of studies have explored the coordination chemistry of classical tripodal ligands containing a range of main-group bridgehead atoms or groups, it is not clear how periodic trends affect ligand character and reactivity within a single ligand family. A case in point is the extensive family of neutral tris-2-pyridyl ligands E(2-py)3 (E=C-R, N, P), which are closely related to archetypal tris-pyrazolyl borates. With the 6-methyl substituted ligands E(6-Me-2-py)3 (E=As, Sb, Bi) in hand, the effects of bridgehead modification alone on descending a single group in the periodic table were assessed. The primary influence on coordination behaviour is the increasing Lewis acidity (electropositivity) of the bridgehead atom as Group 15 is descended, which not only modulates the electron density on the pyridyl donor groups but also introduces the potential for anion selective coordination behaviour.

A General, Rhodium-Catalyzed, Synthesis of Deuterated Boranes and N-Methyl Polyaminoboranes.

The rhodium complex [Rh(Ph2 PCH2 CH2 CH2 PPh2 )(η6 -FC6 H5 )][BArF4 ], 2, catalyzes BH/BD exchange between D2 and the boranes H3 B⋅NMe3 , H3 B⋅SMe2 and HBpin, facilitating the expedient isolation of a variety of deuterated analogues in high isotopic purities, and in particular the isotopologues of N-methylamine-borane: R3 B⋅NMeR2 1-dx (R=H, D; x=0, 2, 3 or 5). It also acts to catalyze the dehydropolymerization of 1-dx to give deuterated polyaminoboranes. Mechanistic studies suggest a metal-based polymerization involving an unusual hybrid coordination insertion chain-growth/step-growth mechanism.