Organometallic Pillarplexes That Bind DNA 4-Way Holliday Junctions and Forks.

Holliday 4-way junctions are key to important biological DNA processes (insertion, recombination, and repair) and are dynamic structures that adopt either open or closed conformations, the open conformation being the biologically active form. Tetracationic metallo-supramolecular pillarplexes display aryl faces about a cylindrical core, an ideal structure to interact with open DNA junction cavities. Combining experimental studies and MD simulations, we show that an Au pillarplex can bind DNA 4-way (Holliday) junctions in their open form, a binding mode not accessed by synthetic agents before. Pillarplexes can bind 3-way junctions too, but their large size leads them to open up and expand that junction, disrupting the base pairing, which manifests in an increased hydrodynamic size and lower junction thermal stability. At high loading, they rearrange both 4-way and 3-way junctions into Y-shaped forks to increase the available junction-like binding sites. Isostructural Ag pillarplexes show similar DNA junction binding behavior but lower solution stability. This pillarplex binding contrasts with (but complements) that of metallo-supramolecular cylinders, which prefer 3-way junctions and can rearrange 4-way junctions into 3-way junction structures. The pillarplexes' ability to bind open 4-way junctions creates exciting possibilities to modulate and switch such structures in biology, as well as in synthetic nucleic acid nanostructures. In human cells, the pillarplexes do reach the nucleus, with antiproliferative activity at levels similar to those of cisplatin. The findings provide a new roadmap for targeting higher-order junction structures using a metallo-supramolecular approach, as well as expanding the toolbox available to design bioactive junction binders into organometallic chemistry.

Separating dissolved silver from nanoparticulate silver is the key: Improved cloud-point-extraction hyphenated to single particle ICP-MS for comprehensive analysis of silver-based nanoparticles in real environmental samples down to single-digit nm particle sizes.

Investigating silver-based nanoparticles (Ag-b-NPs) in environmental samples is challenging with current analytical techniques, owing to their low concentrations (ng L-1) in the presence of high quantities of dissolved Ag(I) species. sp-ICP-MS is a promising technique able to simultaneously determine the concentration and particle sizes of Ag-b-NPs even at concentrations of several ng L-1. However, sp-ICP-MS suffers from the coexistence of dissolved analyte species causing high background signals. These background signals cover particle signals and therefore limit the size detection limit (SDL) in sp-ICP-MS. Ag-b-NPs in environmental samples exhibit diameters of < 20 nm, whereas the current sp-ICP-MS approaches barely reach an SDL as low as 20 nm. Using a surfactant-mediated sample pre-treatment (improved cloud point extraction, iCPE), we were able to separate Ag-b-NPs in aqueous samples from dissolved Ag(I) species and enrich the NPs in the extract. By hyphenating iCPE to sp-ICP-MS, we were able to reach SDL values as low as 4.5 nm, thus paving the way for the successful monitoring of Ag-b-NPs in the environment.

Activation of Molecular Oxygen by a Cobalt(II) Tetra-NHC Complex*.

The first dicobalt(III) µ2 -peroxo N-heterocyclic carbene (NHC) complex is reported. It can be quantitatively generated from a cobalt(II) compound bearing a 16-membered macrocyclic tetra-NHC ligand via facile activation of dioxygen from air at ambient conditions. The reaction proceeds via an end-on superoxo intermediate as demonstrated by EPR studies and DFT. The peroxo moiety can be cleaved upon addition of acetic acid, yielding the corresponding CoIII acetate complex going along with H2 O2 formation. In contrast, both CoII and CoIII complexes are also studied as catalysts to utilize air for olefin and alkane oxidation reactions; however, not resulting in product formation. The observations are rationalized by DFT-calculations, suggesting a nucleophilic nature of the dicobalt(III) µ2 -peroxo complex. All isolated compounds are characterized by NMR, ESI-MS, elemental analysis, EPR and SC-XRD.

Disilene-Silylene Interconversion: A Synthetically Accessible Acyclic Bis(silyl)silylene.

Silylenes have recently shown fascinating reactivity patterns, which are normally observed almost exclusively for transition-metal complexes. In particular, very reactive representatives are considered to be promising candidates, which may become powerful and economical alternatives for catalytic applications in the future. Here, we present the isolation of an equilibrium mixture consisting of a tetrasilyldisilene and its isomeric bis(silyl)silylene, the first isolable silylene of this type. Preliminary investigations demonstrate the extreme inherent reactivity via facile small-molecule activation even under very mild conditions. Thus, the oxidative addition of challenging targets such as H2 and NH3 was achieved. In addition, by synthesizing donor-stabilized bis(silyl)silylenes we gained further insights into the disilene-silylene rearrangement by 1,2-silyl migrations. Thorough theoretical calculations support the observed experimental results.

Non-Innocent Methylene Linker in Bridged Lewis Pair Initiators.

Deprotonation usually occurs as an unwanted side reaction in the Lewis pair polymerization of Michael acceptors, for which the conjugated addition of the Lewis base to the acid-activated monomer is the commonly accepted initiation mechanism. This has also been reported for B-P-based bridged Lewis pairs (BLPs) that form macrocyclic addition products. We now show that the formerly unwanted deprotonation is the likely initiation pathway in the case of Al-P-based BLPs. In a detailed study of a series of Al-P-based BLPs, using a combination of single-crystal diffraction experiments (X-ray and neutron) and mechanistic investigations (experimental and computational), an active role of the methylene bridge was revealed, acting as a base towards the α-acidic monomers. Additionally, the polymerization studies proved a living behavior combined with significantly high activities, narrow molecular mass distributions, and the possibility of copolymerization.

Reactivity of an NHC-stabilized pyramidal hydrosilylene with electrophilic boron sources.

Silylenes have become an indispensable tool for molecular bond activation. Their use for the construction of silicon-boron bonds is uncommon in comparison to the numerous studies on silylene-derived silicon-element bond formations. Herein we investigate the reactivity of the pyramidal NHC-coordinated hydrosilylene tBu3SiSi(H)LMe4 (1; NHC = N-heterocyclic carbene, LMe4 = 1,3,4,5-tetramethylimidazolin-2-ylidene) with various boron-centered electrophiles. The reaction of 1 with THF·BH3 or H3N→BH3 afforded the silylene complex 1→BH3 or the product of insertion of the silicon(ii) atom into an N-H bond with concomitant dehydrogenation along the HN-BH moiety (2). The respective conversion of 1 with BPh3 yields 1→BPh3 which readily reacts with excess LMe4 to form the more stable complex LMe4→BPh3 with release of 1. Treatment of 1 with the haloboranes Et2O→BF3, BCl3, BBr3 and Me2S→BBr3 resulted in the formation of the Lewis acid base adducts 1→BX3 (X = F, Cl, Br) and an equilibrium with their auto-ionization products [12BX2]+[BX4]- slowly develops. The ratio of 1→BX3 significantly increases with rising atomic number of the halide, thus 1→BF3 majorly transforms within hours while 1→BBr3 is near-quantitatively retained over time. Accordingly, the complex 1→BPhBr2 was isolated after conversion of 1 with PhBBr2.

Discovery of Polyoxo-Noble-Metalate-Based Metal-Organic Frameworks.

Here we report on the synthesis, structure, and characterization of the first example of a polyoxopalladate (POP)-based metal-organic framework (MOF). This novel class of materials comprises discrete polyoxo-13-palladate(II) nanocubes [Pd13O8(AsO4)8H6]8- decorated by four Ba2+ ions on each of two opposite faces. These secondary building units (SBUs) are linked to each other via rigid linear organic groups, resulting in a stable 3D POP-MOF framework, which exhibits interesting sorption as well as catalytic properties.

The Quest for Stable Silaaldehydes: Synthesis and Reactivity of a Masked Silacarbonyl.

The first donor-acceptor complex of a silaaldehyde, with the general formula (NHC)(Ar)Si(H)OGaCl3 (NHC=N-heterocyclic carbene), was synthesized using the reaction of silyliumylidene-NHC complex [(NHC)2 (Ar)Si]Cl with water in the presence of GaCl3 . Conversion of this complex to the corresponding silacarboxylate dimer [(NHC)(Ar)SiO2 GaCl2 ]2 , free silaacetal ArSi(H)(OR)2 , silaacyl chloride (NHC)(Ar)Si(Cl)OGaCl3 , and phosphasilene-NHC adduct (NHC)(Ar)Si(H)PTMS unveil its true potential as a synthon in silacarbonyl chemistry.

A bench stable formal Cu(iii) N-heterocyclic carbene accessible from simple copper(ii) acetate.

For years, Cu(iii)NHCs have been proposed as active intermediates in Cu(i)NHC catalyzed reactions, yielding the desired products by reductive elimination, but until today, no one has ever reported the characterisation of such a compound. When working on the synthesis of biomimetic transition metal (NHC) complexes and their application in homogeneous catalysis, we recently found a highly unusual reactivity for Cu(ii) acetate in the presence of a particular cyclic tetra(NHC) ligand. Therein, the formation of the first stable CuNHC compound, displaying Cu in the formal oxidation state +III, by simple disproportionation of Cu(ii) acetate in dimethyl sulfoxide (DMSO) was observed. At elevated temperatures selective mono-oxidation of the NHC ligand occurs, even under anaerobic conditions. Acetate was identified as the origin of the oxygen atom by 18O-labelling experiments. The remarkably high stability of the title compound was furthermore proven electrochemically by cyclic voltammetry. An in-depth investigation of its reactivity revealed the involvement of four additional compounds. Three of them could be isolated and characterised by 1H/13C-NMR, single crystal XRD, mass spectrometry and elemental analysis. The fourth, a Cu(i)NHC intermediate, formed by formal reductive elimination from the Cu(NHC)3+ compound, was characterised in situ by 1H/13C-NMR and computational methods.

Antimicrobial Activity and Cytotoxicity of Ag(I) and Au(I) Pillarplexes.

The biological activity of four pillarplex compounds featuring different metals and anions was investigated. The toxicity of the compounds against four bacterial strains [Bacillus subtilis (ATCC6633), Staphylococcus aureus (ATCC6538), Escherichia coli (UVI isolate), Pseudomonas aeruginosa], one fungus (Candida albicans), and a human cell line (HepG2) was determined. Additionally, a UV-Vis titration study of the pillarplexes was carried out to check for stability depending on pH- and chloride concentration changes and evaluate the applicability in physiological media. All compounds are bioactive: the silver compounds showed higher activity against bacteria and fungi, and the corresponding gold pillarplexes were less toxic against human cells.

Stereochemistry of the Menthyl Grignard Reagent: Generation, Composition, Dynamics, and Reactions with Electrophiles.

Menthyl Grignard reagent 1 from either menthyl chloride (2) or neomenthyl chloride (3) consists of menthylmagnesium chloride (1a), neomenthylmagnesium chloride (1b), trans- p-menthane (4), 2-menthene (8), 3-menthene (9), and Wurtz coupling products including symmetrical bimenthyl 13. The diastereomeric ratio 1a/1b was determined in situ by 13C NMR or after D2O quenching by 2H NMR analysis. Hydrolysis of the C-Mg bond proceeds with retention of configuration at C-1. The kinetic ratio 1a/1b from Grignard reagent generation (dr 59:41 at 50 °C in THF) is close to the thermodynamic ratio (56:44 at 50 °C in THF). Carboxylation of 1 at -78 °C separates diastereomers 1a/b to give the anion of menthanecarboxylic acid (19) from 1a, which combines with unreactive 1b to give neomenthylmagnesium menthanecarboxylate (1bI). The kinetics of epimerization for the menthyl/neomenthylmagnesium system was analyzed (Δ H⧧ = 98.5 kJ/mol, Δ S⧧ = -113 J/mol·K for 1bI → 1aI). Reactions of 1 with phosphorus electrophiles proceed stereoconvergently at C-1 of 1a/b to give predominantly menthyl-configured substitution products: PCl3 and 2 equiv of 1 give Men2PCl (6), which hydrolyzes to dimenthylphosphine P-oxide (7), whereas Ph2PCl with 1 equiv of 1 gave P-menthyldiphenylphosphine oxide (27) after workup in air.

Synthesis of Lewis Acidic, Aromatic Aminotroponiminate Zinc Complexes for the Ring-Opening Polymerization of Cyclic Esters.

Three novel aminotroponiminate (ATI) zinc complexes I-III (I = [(Ph2)ATI]Zn-N(SiMe3)2, II = [(C6H3-2,6-C2H5/Ph)ATI]Zn-N(SiMe3)2, and III = [(C6H3-2,6-CH(CH3)2/Ph)ATI]Zn-N(SiMe3)2) were synthesized and tested in the ring-opening polymerization of the lactones ß- rac-butyrolactone (BBL) and rac-lactide (LA). The ligands, with two of them literature unknown, were readily obtained via a three-step synthesis from tropolone. Forming a five-membered metallacycle with zinc, the complexes were further structurally examined via single-crystal X-ray analysis and compared with that of the established, 6-ringed ß-diiminate (BDI) complex IV ([CH(CMeNPh)2]Zn-N(SiMe3)2). The influence of the varying metallacycle ring size on the polymerization was evaluated. In situ IR measurements indicate a higher catalytic activity of the novel ATI complexes I-III for BBL compared with the BDI system IV. The activity and degree of control were further improved by an in situ generated alkoxy initiating group generated after the addition of 2-propanol. An enhanced initiator efficiency allowed the synthesis of polymers with controlled molecular weights and narrow polydispersities. Furthermore, II and III exhibited a high activity in the ring-opening polymerization of rac-LA. Hereby, reaction time and initiator efficiency could also be optimized at a higher temperature or by the addition of 2-propanol.

Single-Site, Organometallic Aluminum Catalysts for the Precise Group Transfer Polymerization of Michael-Type Monomers.

Unlike different types of Lewis pairs as polymerization catalysts for acrylic monomers, organometallic aluminum(III) compounds are reported that show a surprisingly high polymerization activity even without an additional Lewis base. DFT calculations, end group analysis and kinetic investigations clearly suggest a main group element (MGE) group transfer polymerization (GTP) mechanism analogous to the known metal-mediated GTP mechanism. The novel catalysts perform a precision polymerization of a broad variety of monomers, ranging from 2-isopropenyl-2-oxazoline to tert-butylmethacrylate and N,N-dimethylacrylamide. Additionally, extended Michael-type structures like 4-vinyl pyridine are accessible. Especially the Al(III) half-metallocenes show an almost quantitative initiator efficiency, and, combined with the living character of the polymerization reactions, they enable the synthesis of block copolymers, even with unconventional monomers like vinyl phosphonates.

Precise Activation of Ammonia and Carbon Dioxide by an Iminodisilene.

The activation of NH3 and CO2 is still an ambitious target for multiply bonded sub-valent silicon compounds. Now, the precise splitting of the N-H bond of ammonia by (Z)-imino(silyl)disilene 1 to give trans-1,2-adduct 2 a at low temperatures (-78 °C) is presented. According to DFT calculations, the stereospecific hydroamination follows a similar mechanism as the recently reported anti-addition of H2 to the Si=Si bond of 1. The aminosilane 2 b could also be obtained as the formal silylene addition product under thermodynamic reaction control. By applying low temperatures, the activation of CO2 with 1 selectively afforded the cis-oxadisilacyclobutanone 7-c as [2+2] cycloadduct. By performing the reaction directly at ambient temperatures, a mixture of three different-sized silacycles (4-6) was observed. Their formation was investigated theoretically and their structures were revealed with separate experiments using 1 and the oxygenation agents N2 O and O2 .

Redox and photocatalytic properties of a NiII complex with a macrocyclic biquinazoline (Mabiq) ligand.

We present a late, first row transition metal photosensitizer that promotes photocatalytic C-C bond formation. The title compound, [Ni(Mabiq)]OTf, as well as its one-electron reduced form, Ni(Mabiq), were synthesized and molecular structures of both were obtained. The electronic structure of the reduced complex additionally was characterized by spectroscopic and DFT computational methods. Notably, [NiII(Mabiq)]OTf is photoactive: reduction of the compound was achieved photochemically upon irradiation at λ = 457 nm and reductive quenching by NEt3. The performance of [Ni(Mabiq)]OTf as a photoredox catalyst was examined in the cyclization of a bromoalkyl-substituted indole. In this reaction, the first-row transition metal compound is comparable if not superior to [Ru(bpy)3]2+ in terms of efficiency (turnover number) and chemoselectivity. Studies using a series of sacrificial donor amines indicate that the excited state redox potential of [Ni(Mabiq)]+* is ≥1.25 V vs. SCE. This value is similar to the excited state potential of commonly employed noble metal based photocatalysts. The Ni-Mabiq compound thus provides a rare example of an earth-abundant photoredox catalyst.

Structural Characterization and Photochemical Properties of Mono- and Bimetallic Cu-Mabiq Complexes.

We present a series of monometallic ([Cu(Mabiq)OTf] (1) and [Cu(Mabiq)] (2)) and bimetallic copper-Mabiq complexes ([Cu2(Mabiq)(PPh3)2(OTf)2] (3) and [Cu2(Mabiq)(PPh3)2]PF6 (4)). The latter compounds contain an additional CuI center that binds in a tetrahedral fashion to the external bipyrimidine nitrogens of the macrocyclic ligand. Compounds 3 and 4 represent the first examples of bimetallic transition metal Mabiq complexes, stable both in solution and in the solid state. The structural and electronic properties of compounds 1-4 were analyzed by means of X-ray crystallography, cyclic voltammetry, and spectroscopic methods. One-electron reduced 2 and 4 consist of a CuII ion coordinated by a Mabiq ligand radical, [CuII(Mabiq•)]. Thus, both bimetallic compounds are mixed-valent with respect to the copper oxidation states. Complexes 2 and 4 can be generated photochemically, upon irradiation of 1 or 3 with visible light in the presence of a sacrificial electron donor.

Synthesis, characterization and derivatization of hydroxyl-functionalized iron(ii) bis(NHC) complexes.

The syntheses of a novel hydroxyl-functionalized tetradentate NHC/pyridine hybrid ligand and the corresponding Ag(i) and Fe(ii) complexes are presented. Spectroscopic and X-ray diffraction techniques are used for structural investigations and cyclic voltammetry measurements reveal interesting electronic properties. Transmetalation of the trinuclear Ag(i) complex (C1) yields a mononuclear and a dinuclear iron(ii) bis(NHC) complex (C2 and C3), which can be separated by stepwise precipitation. The former is isostructural to iron(ii) bis(NHC) complex A, which is a versatile oxidation catalyst. Furthermore, suitable conditions for esterification reactions of the ligand precursor and iron(ii) bis(NHC) complex (C2) have been established, demonstrating the utility of the hydroxyl functionality for immobilization and derivatization purposes.

Silicon and Oxygen's Bond of Affection: An Acyclic Three-Coordinate Silanone and Its Transformation to an Iminosiloxysilylene.

A long-term dream comes true: An acyclic, neutrally charged silanone at last! Here, we report on the first examples of isolable acyclic, neutral, three-coordinate silanones 2 with indefinite stability as solids and lifetimes in solution of up to 2 days. The electronic properties of the Si═O bond were investigated via DFT calculations and revealed the π-donating N-heterocyclic imino (NHI) and σ-donating silyl groups as key factors for their enhanced stability. Besides initial reactivity studies of 2 toward CO2 and methanol, different isomerization pathways depending on the silyl substitution pattern were found. For 2a (R = TMS), a 1,3-silyl shift gave an intermediary disilene, which was trapped as unique NHC-disilene adduct 6. For the more stable silanone 2b (R = t-Bu), a selective transformation to the first reported room temperature stable, acyclic, two-coordinate N,O-silylene 7 exhibiting a fascinating siloxy ligand was observed. Both compounds were fully characterized experimentally and their bonding features were analyzed by theoretical calculations.

A hybrid imidazolylidene/imidazolium nickel NHC complex: an isolated intermediate.

Macrocyclic ligand systems with a variety of (different) donor sites oftentimes give rise to very exciting and unexpected multinuclear metal complexes. We report herein the structure of a trinuclear mixed imidazolylidene/imidazolium nickel N-heterocyclic carbene (NHC) complex, namely di-µ-chlorido-bis{µ-calix[2]imidazolium[2]imidazolylidene[2]pyrazolate}trinickel(II) tetrakis(hexafluoridophosphate) acetonitrile tetrasolvate, [Ni3(C24H24N12)2Cl2](PF6)4·4CH3CN or [Ni3(LMe)2Cl2](PF6)4·4CH3CN, that can be understood as a trapped reaction intermediate during the synthesis of the respective [Ni2LMe](PF6)2 product. The structure not only contains protonated next to deprotonated imidazole heterocycles, but also Ni2+ ions with fundamentally different coordination modes within one molecule. Two of the three metal atoms are coordinated in a square-pyramidal fashion by half a ligand molecule and one chloride ligand, whereas the third Ni2+ ion is bound octahedrally by four pyrazolate moieties and two chloride anions.

A pH-Dependent, Mechanically Interlocked Switch: Organometallic [2]Rotaxane vs. Organic [3]Rotaxane.

We present the first [2]rotaxane featuring a functional organometallic host. In contrast to the known organic scaffolds, this assembly shows a high post-synthetic modifiability. The reactivity of the Ag8 pillarplex host is fully retained, as is exemplified by the first transmetalation in a rotaxane framework to provide the respective Au8 analogue. Additionally, a transformation under acidic conditions to give a purely organic [3]rotaxane is demonstrated which is reversible upon addition of a suitable base, rendering the assembly a pH-dependent switch. Hereby, it is shown that the mechanically interlocked nature of the system enhances the kinetic stability of the NHC host complex by a factor of >1000 and corresponds to the first observation of a stabilizing "rotaxand effect".