Search Results (17)

The ferrocidiphenol family brings together anticancer molecules featuring a [ferrocene-alkene-(p-phenol)₂] motif that can form upon oxidation a quinone methide metabolite targeting cellular proteins. Adding an imide group (imido-ferrocidiphenol) dramatically enhanced the anticancer activity of ferrocidiphenol. We aimed to explore whether molecules with two ferrociphenol motifs connected by bisimide moieties could provide even more effective compounds. Using amino-ferrocidiphenol and commercial bisanhydrides at reflux, for the first time, three symmetrical and bent bis(imido-ferrocidiphenols) were synthesized, with moderate yields, and characterized. However, these compounds were insoluble in most common organic solvents and unstable. This likely explains why their anticancer activity was nil. Full article

The potassium alumanyl [{SiN^Dipp}AlK]₂ (SiN^Dipp = {CH₂SiMe₂NDipp}₂; Dipp = 2,6-i-Pr₂C₆H₃) reacts with organic azides via reductive N₂ elimination. With the less sterically encumbered azides PhN₃ and C₁₀H₁₅N₃ (1-azidoadamantane), the putative initially formed aluminium imide undergoes facile [2 + 3] cycloaddition to provide the tetrazenylaluminates [{SiN^Dipp}Al-κ²-N,N′-({N(R)}₂N₂)]K (R = Ph, C₁₀H₁₅). In contrast, each Al(I) centre of [{SiN^Dipp}AlK]₂ only reacts with a single equivalent of 2,4,6-Me₃C₆H₂N₃ to provide the imidoaluminate [{SiN^Dipp}AlN(2,4,6-Me₃C₆H₂)(K∙C₆H₆)], which crystallises as a monomer and displays a short Al-N distance of 1.7040(13) Å. Attempts to synthesise the azide [{SiN^Dipp}AlN₃] by reaction of [{SiN^Dipp}AlI] with an excess of KN₃ resulted in exclusive formation of the bis(azido)aluminate [{SiN^Dipp}Al(N₃)₂K], which crystallises as an infinite 1-dimensional polymer propagated by μ-(1,3)-N₃ bridging interactions between the potassium cations and azide anions. Although the THF-adducted azide [{SiN^Dipp}AlN₃(THF)] may be synthesised and characterised by more stringent control of the reaction stoichiometry, the synthetic viability of this route remains compromised by competitive generation of [{SiN^Dipp}Al(N₃)₂K]. Full article

This review article is focused on the progress made in the synthesis of 5′-α-P-modified nucleoside triphosphates (α-phosphate mimetics). A variety of α-P-modified nucleoside triphosphates (NTPαXYs, Y = O, S; X = S, Se, BH₃, alkyl, amine, N-alkyl, imido, or others) have been developed. There is a unique class of nucleoside triphosphate analogs with different properties. The main chemical approaches to the synthesis of NTPαXYs are analyzed and systematized here. Using the data presented here on the diversity of NTPαXYs and their synthesis protocols, it is possible to select an appropriate method for obtaining a desired α-phosphate mimetic. Triphosphates’ substrate properties toward nucleic acid metabolism enzymes are highlighted too. We reviewed some of the most prominent applications of NTPαXYs including the use of modified dNTPs in studies on mechanisms of action of polymerases or in systematic evolution of ligands by exponential enrichment (SELEX). The presence of heteroatoms such as sulfur, selenium, or boron in α-phosphate makes modified triphosphates nuclease resistant. The most distinctive feature of NTPαXYs is that they can be recognized by polymerases. As a result, S-, Se-, or BH₃-modified phosphate residues can be incorporated into DNA or RNA. This property has made NTPαXYs a multifunctional tool in molecular biology. This review will be of interest to synthetic chemists, biochemists, biotechnologists, or biologists engaged in basic or applied research. Full article

The interactions with calf thymus DNA (CT-DNA) of three Schiff bases formed by the condensation of hesperetin with benzohydrazide (HHSB or L¹H₃), isoniazid (HIN or L²H₃), or thiosemicarbazide (HTSC or L³H₃) and their Cu^II complexes (CuHHSB, CuHIN, and CuHTSC with the general formula [CuLⁿH₂(AcO)]) were evaluated in aqueous solution both experimentally and theoretically. UV–Vis studies indicate that the ligands and complexes exhibit hypochromism, which suggests helical ordering in the DNA helix. The intrinsic binding constants (K_b) of the Cu compounds with CT-DNA, in the range (2.3–9.2) × 10⁶, from CuHTSC to CuHHSB, were higher than other copper-based potential drugs, suggesting that π–π stacking interaction due to the presence of the aromatic rings favors the binding. Thiazole orange (TO) assays confirmed that ligands and Cu complexes displace TO from the DNA binding site, quenching the fluorescence emission. DFT calculations allow for an assessment of the equilibrium between [Cu(LⁿH₂)(AcO)] and [Cu(LⁿH₂)(H₂O)]⁺, the tautomer that binds Cu^II, amido (am) and not imido (im), and the coordination mode of HTSC (O⁻, N, S), instead of (O⁻, N, NH₂). The docking studies indicate that the intercalative is preferred over the minor groove binding to CT-DNA with the order [Cu(L¹H₂^am)(AcO)] > [Cu(L²H₂^am)(AcO)] ≈ TO ≈ L¹H₃ > [Cu(L³H₂^am)(AcO)], in line with the experimental K_b constants, obtained from the UV–Vis spectroscopy. Moreover, dockings predict that the binding strength of [Cu(L¹H₂^am)(AcO)] is larger than [Cu(L¹H₂^am)(H₂O)]⁺. Overall, the results suggest that when different enantiomers, tautomers, and donor sets are possible for a metal complex, a computational approach should be recommended to predict the type and strength of binding to DNA and, in general, to macromolecules. Full article

The present work demonstrates the optimization of the ligand structure in the series of bis(phosphine oxide) and β-ketophosphine oxide representatives for efficient coordination of Tb³⁺ and Eu³⁺ ions with the formation of the complexes exhibiting high Tb³⁺- and Eu³⁺-centered luminescence. The analysis of the stoichiometry and structure of the lanthanide complexes obtained using the XRD method reveals the great impact of the bridging group nature between two phosphine oxide moieties on the coordination mode of the ligands with Tb³⁺ and Eu³⁺ ions. The bridging imido-group facilitates the deprotonation of the imido- bis(phosphine oxide) ligand followed by the formation of tris-complexes. The spectral and PXRD analysis of the separated colloids indicates that the high stability of the tris-complexes provides their safe conversion into polystyrenesulfonate-stabilized colloids using the solvent exchange method. The red Eu³⁺-centered luminescence of the tris-complex exhibits the same specificity in the solutions and the colloids. The pronounced luminescent response on the antibiotic ceftriaxone allows for sensing the latter in aqueous solutions with an LOD value equal to 0.974 μM. Full article

Polyazomethines containing electron-donor triphenylamine (TPA) or carbazole (Cbz) and electron-acceptor naphthyl(di)imide were synthesized and investigated with regard to thermal, optical and electronic features, with a focus on their modulation by molecular design. The polycondesation of an imido-based diamine with a Cbz- or TPA-based dialdehyde led to donor-acceptor polymers with good thermostability, up to 318 °C. These displayed good solubility in organic solvents, which enabled easy polymer processability in thin films with different molecular assemblies. The molecular order improved the charge carrier’s mobility, with a direct impact on the bandgap energy. The optical properties studied by UV–Vis absorption and fluorescence experiments showed solvent-dependence, characteristic for donor-acceptor systems. The structural parameters exerted a strong influence on the light-emissive behavior, with the prevalence of intrinsic or intramolecular charge transfer fluorescence contingent on the donor-acceptor strength and polymer geometry. All polymers showed good electroactivity, supporting both electrons and holes transport. The exchange of Cbz with TPA proved to be an efficient tool with which to decrease the bandgap energy, while that of naphthyl(di)imide with bis(naphthylimide) was beneficial for fluorescence enhancement. This study may contribute to a deeper understanding of the physico-chemistry of electronic materials so as to make them more competitive in the newest energy-related or other optoelectronic devices. Full article

Treatment of Mn(N(SiMe₃)₂)₂(THF)₂ with bulky chelating bis(alkoxide) ligand [1,1′:4′,1′′-terphenyl]-2,2′′-diylbis(diphenylmethanol) (H₂[O-terphenyl-O]^Ph) formed a seesaw manganese(II) complex Mn[O-terphenyl-O]^Ph(THF)₂, characterized by structural, spectroscopic, magnetic, and analytical methods. The reactivity of Mn[O-terphenyl-O]^Ph(THF)₂ with various nitrene precursors was investigated. No reaction was observed between Mn[O-terphenyl-O]^Ph(THF)₂ and aryl azides. In contrast, the treatment of Mn[O-terphenyl-O]^Ph(THF)₂ with iminoiodinane PhINTs (Ts = p-toluenesulfonyl) was consistent with the formation of a metal-nitrene complex. In the presence of styrene, the reaction led to the formation of aziridine. Combining varying ratios of styrene and PhINTs in different solvents with 10 mol% of Mn[O-terphenyl-O]^Ph(THF)₂ at room temperature produced 2-phenylaziridine in up to a 79% yield. Exploration of the reactivity of Mn[O-terphenyl-O]^Ph(THF)₂ with various olefins revealed (1) moderate aziridination yields for p-substituted styrenes, irrespective of the electronic nature of the substituent; (2) moderate yield for 1,1′-disubstituted α-methylstyrene; (3) no aziridination for aliphatic α-olefins; (4) complex product mixtures for the β-substituted styrenes. DFT calculations suggest that iminoiodinane is oxidatively added upon binding to Mn, and the resulting formal imido intermediate has a high-spin Mn(III) center antiferromagnetically coupled to an imidyl radical. This imidyl radical reacts with styrene to form a sextet intermediate that readily reductively eliminates the formation of a sextet Mn(II) aziridine complex. Full article

Uranyl ions, {UO₂}ⁿ⁺ (n = 1, 2), display trans, strongly covalent, and chemically robust U-O multiple bonds, where 6d, 5f, and 6p orbitals play important roles. The synthesis of isoelectronic analogues of uranyl has been of interest for quite some time, mainly with the purpose of unveiling covalence and 5f-orbital participation in bonding. Significant advances have occurred in the last two decades, initially marked by the synthesis of uranium(VI) bis(imido) complexes, the first analogues with a {RNUNR}²⁺ core, later followed by the synthesis of unique trans-{EUO}²⁺ (E = S, Se) complexes, and recently highlighted by the synthesis of the first complexes featuring a linear {NUN} moiety. This review covers the synthesis, structure, bonding, and reactivity of uranium complexes containing a linear {EUE}ⁿ⁺ core (n = 0, 1, 2), isoelectronic to uranyl ions, {OUO}ⁿ⁺ (n = 1, 2), incorporating σ- and π-donating ligands that can engage in uranium–ligand multiple bonding, where oxygen may be replaced by heavier chalcogenido, imido, nitride, and carbene ligands, or by a transition metal. It focuses on synthetic methods of well-defined molecular uranium species in the condensed phase but also references gas-phase and low-temperature-matrix experiments, as well as computational studies that may lead to valuable insights. Full article

The reaction of [Mo(η-C₅Me₅)Cl₄] with the ortho-, meta-, or para-iodo-functionalized anilines 2-IC₆H₄NH₂, 3-IC₆H₄NH₂, 4-IC₆H₄NH₂ yields imido or amine products of the type [Mo(η-C₅Me₅)Cl₂(IC₆H₄N)] (2-I, 1, 3-I, 3, 4-I, 5) or [Mo(η-C₅Me₅)Cl₄(IC₆H₄NH₂)] (3-I, 2, 4-I, 4), respectively, depending on the reaction stoichiometry/conditions; we were unable to isolate an amine complex of the 2-I derivative. The reaction of [Mo(η-C₅Me₅)Cl₄] with one equivalent of 2-I,4-FC₆H₃NH₂ in the presence of Et₃N afforded [Mo(η-C₅Me₅)Cl₂(2-I,4-FC₆H₃N)]·MeCN (6·MeCN), which, upon exposure to air, afforded the Mo(VI) imido complex [Mo(η-C₅Me₅)Cl₃(2-I,4-FC₆H₃N)] (7). For comparative studies, the structure of the aniline (C₆H₅NH₂)-derived complex [Mo(η-C₅Me₅)Cl₂(2-C₆H₃N)] (8) has also been prepared. The molecular structures of 1–8 have been determined and reveal packing in the form of zig-zag chains or ladders. The complexes catalyze, in the presence of benzyl alcohol under N₂, the ring-opening polymerization (ROP) of ε-caprolactone affording relatively low molecular weight products. The MALDI-ToF spectra indicate that a number of polymer series bearing a variety of end groups are formed. Conducting the ROPs as melts or under air results in the isolation of higher molecular weight products, again bearing a variety of end groups. Kinetic studies reveal the aniline-derived imido complex 8 performs best, whilst a meta-iodo substituent and a Mo(V) centre are also found to be beneficial. The structures of the side products 2-IC₆H₄NH₃Cl and 3-IC₆H₄NH₃Cl are also reported. Full article

Density functional theory and time-dependent density functional theory have been enacted to investigate the effects of donor and acceptor on the first hyperpolarizability of Lindquist-type organo-imido polyoxometalates (POMs). These calculations employ a range-separated hybrid exchange-correlation functional (ωB97X-D), account for solvent effects using the implicit polarizable continuum model, and analyze the first hyperpolarizabilities by using the two-state approximation. They highlight the beneficial role of strong donors as well as of π-conjugated spacers (CH=CH rather than C≡C) on the first hyperpolarizabilities. Analysis based on the unit sphere representation confirms the one-dimensional push-pull π-conjugated character of the POMs substituted by donor groups and the corresponding value of the depolarization ratios close to 5. Furthermore, the use of the two-state approximation is demonstrated to be suitable for explaining the origin of the variations of the first hyperpolarizabilities as a function of the characteristics of a unique low-energy charge-transfer excited state and to attribute most of the first hyperpolarizability changes to the difference of dipole moment between the ground and that charge-transfer excited state. Full article

In this article, we describe the synthesis of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) adducts of rhodium(II) carboxylate complexes, [Rh₂(μ-O₂CCR₃)₄(DBU)₂] (R = H (1), Me (2)). The DBU ligand is coordinated to the axial site in both adducts via the imido-nitrogen atom, and single-crystal X-ray diffraction analysis of 1 and 2 revealed structurally similar attributes between the compounds. The Rh–Rh bond distance is 2.4108(3) Å for 1 and 2.4143(2) Å for 2. The Rh–N distance is 2.2681(3) Å for compound 1 and 2.2587(10) Å for compound 2. Compound 1, however, crystallized with solvent molecules in its unit cell, and Hirshfeld surface analysis showed intermolecular C–H···O interactions between oxygen atoms of [Rh₂(μ-O₂CCH₃)₄] and the hydrogen of the chloroform solvent among other intermolecular close-contact interactions. The crystal structure of compound 2 was found to be devoid of solvent and showed weak intramolecular C–H···O interactions from the DBU axial ligand to the oxygens of the bridging acetates. Otherwise, Hirshfeld analysis showed that 2 was dominated by H···H interactions. UV-vis spectroscopy of both adducts was also conducted in different solvents to examine shifts attributed to the π*(Rh₂) to σ*(Rh₂) band. Full article

Rhizopus spp. are the most common etiological agents of mucormycosis, causing over 90% mortality in disseminated infections. The diagnosis relies on histopathology, culture, and/or polymerase chain reaction. For the first time, the glycosylation of rhizoferrin (RHF) was described in a Rhizopus microsporus clinical isolate by liquid chromatography and accurate tandem mass spectrometry. The fermentation broth lyophilizate contained 345.3 ± 13.5, 1.2 ± 0.03, and 0.03 ± 0.002 mg/g of RHF, imido-RHF, and bis-imido-RHF, respectively. Despite a considerable RHF secretion rate, we did not obtain conclusive RHF detection from a patient with disseminated mucormycosis caused by the same R. microsporus strain. We hypothesize that parallel antimycotic therapy, RHF biotransformation, and metabolism compromised the analysis. On the other hand, the full profile of posaconazole metabolites was retrieved by our in house software CycloBranch. Full article

Synthesis of new chromium(II) complexes with chelating bis(alkoxide) ligand [OO]^Ph (H₂[OO]^Ph = [1,1′:4′,1′’-terphenyl]-2,2′’-diylbis(diphenylmethanol)) and their subsequent reactivity in the context of catalytic production of carbodiimides from azides and isocyanides are described. Two different Cr(II) complexes are obtained, as a function of the crystallization solvent: mononuclear Cr[OO]^Ph(THF)₂ (in toluene/THF, THF = tetrahydrofuran) and dinuclear Cr₂([OO]^Ph)₂ (in CH₂Cl₂/THF). The electronic structure and bonding in Cr[OO]^Ph(THF)₂ were probed by density functional theory calculations. Isolated Cr₂([OO]^Ph)₂ undergoes facile reaction with 4-MeC₆H₄N₃, 4-MeOC₆H₄N₃, or 3,5-Me₂C₆H₃N₃ to yield diamagnetic Cr(VI) bis(imido) complexes; a structure of Cr[OO]^Ph(N(4-MeC₆H₄))₂ was confirmed by X-ray crystallography. The reaction of Cr₂([OO]^Ph)₂ with bulkier azides N₃R (MesN₃, AdN₃) forms paramagnetic products, formulated as Cr[OO]^Ph(NR). The attempted formation of a Cr–alkylidene complex (using N₂CPh₂) instead forms chromium(VI) bis(diphenylmethylenehydrazido) complex Cr[OO]^Ph(NNCPh₂)₂. Catalytic formation of carbodiimides was investigated for the azide/isocyanide mixtures containing various aryl azides and isocyanides. The formation of carbodiimides was found to depend on the nature of organoazide: whereas bulky mesitylazide led to the formation of carbodiimides with all isocyanides, no carbodiimide formation was observed for 3,5-dimethylphenylazide or 4-methylphenylazide. Treatment of Cr₂([OO]^Ph)₂ or H₂[OO]^Ph with NO⁺ leads to the formation of [1,2-b]-dihydroindenofluorene, likely obtained via carbocation-mediated cyclization of the ligand. Full article

Solution V K-edge XANES (X-ray absorption near edge structure) and EXAFS (extended X-ray absorption fine structure) analysis of vanadium(V) complexes containing both imido ligands and anionic ancillary donor ligands (L) of type, V(NR)(L)X₂ (R = Ar, Ad (1-adamantyl); Ar = 2,6-Me₂C₆H₃; X = Cl, Me, L = 2-(ArNCH₂)C₅H₄N, OAr, WCA-NHC, and 2-(2’-benzimidazolyl)pyridine; WCA-NHC = anionic NHCs containing weak coordinating B(C₆F₅)₃), which catalyze ethylene dimerization and/or polymerization in the presence of Al cocatalysts, has been explored. Different catalytically actives species with different oxidation states were formed depending upon the Al cocatalyst (MAO, Me₂AlCl, AlⁱBu₃, etc.) and the anionic ancillary donor ligand employed. The method is useful for obtainment of the direct information of the active species (oxidation state, basic framework around the centered metal) in solution, and for better understanding in catalysis mechanism and organometallic as well as coordination chemistry. Full article

Two new aromatic organo-imido polyoxometalates with an electron donor triazole group ([n-Bu₄N]₂[Mo₆O₁₈NC₆H₄N₃C₂H₂]) (1) and a highly conjugated fluorene ([n-Bu₄N]₂[Mo₆O₁₈NC₁₃H₉]) (2) have been obtained. The electrochemical and spectroscopic properties of several organo-imido systems were studied. These properties were analysed by the theoretical study of the redox potentials and by means of the excitation analysis, in order to understand the effect on the substitution of the organo-imido fragment and the effect of the interaction to a metal centre. Our results show a bathochromic shift related to the charge transfer processes induced by the increase of the conjugated character of the organic fragment. The cathodic shift obtained from the electrochemical studies reflects that the electronic communication and conjugation between the organic and inorganic fragments is the main reason of this phenomenon. Full article