Application of the intramolecular Diels-Alder vinylarene (IMDAV) reaction for the synthesis of benzo-, carbocyclo-, thienothiopheneisoindolecarboxylic acids and its limitations.

Thienylallylamines, readily accessible from the corresponding thienyl aldehydes, react with maleic and trifluoromethylmaleic anhydrides leading to the formation of acids with a thieno[2,3-f]isoindole core. The reaction sequence involves two successive steps: acylation of the nitrogen atom of the initial allylamine and the intramolecular Diels-Alder vinylarene (IMDAV) reaction. The scope and limitations of the proposed method were thoroughly investigated. It has been revealed with the aid of X-ray analysis and DFT calculations that the key step, the IMDAV reaction, proceeds through an exo-transition state, giving rise to the exclusive formation of a single diastereomer of the target heterocycle. The obtained functionally substituted thieno[2,3-f]isoindole carboxylic acids are potentially useful substrates for further transformations and bioscreening. The antimicrobial evaluation of the obtained compounds revealed that 1-oxo-2-(3-(trifluoromethyl)phenyl)hexahydrobenzo[4,5]thieno[2,3-f]isoindole-10-carboxylic acid is the most active sample in the synthesized library. It exhibits antibacterial activity against sensitive strains of Gram-positive bacteria, including S. aureus, Enterococcus faecium, Bacillus cereus, and Micrococcus luteus, as well as the Gram-negative bacteria E. coli and Pseudomonas fluorescens, with MIC values ranging from 4 to 64 µg mL-1. 9-Oxo-8-phenyloctahydronaphtho[2,1-d]thieno[2,3-f]isoindole-10-carboxylic acid showed antifungal activity against yeast culture C. albicans with a MIC value of 32 µM.

Domino Three-Component N-Acylation/[4 + 2] Cycloaddition/Alder-ene Synthesis of Polysubstituted Benzo[f]isoindole-4-carboxylic Acids.

Diversely substituted, partially saturated benzo[f]isoindole-4-carboxylic acids were synthesized by a new three-component reaction (3CR) starting from cinnamic amines (3-arylallylamines), maleimides, and maleic anhydride. The process consists of N-acylation of the amines by maleic anhydride, intramolecular [4 + 2] cycloaddition in vinylarenes (the IMDAV reaction), and the concluding Alder-ene reaction between Diels-Alder intermediates and maleimides. All of the reaction steps proceed in a highly regio- and stereoselective manner, furnishing five adjacent chiral centers and leading to a single diastereoisomer of the title compound. The efficiency of the transformation is secured by thermal conditions or utilization of soft Lewis acids (Yb(OTf)3) as catalysts. The kinetics and mechanism of the 3CR were studied by using dynamic 19F NMR. Based on the NMR data and density functional theory (DFT) calculations, the IMDAV, not the Alder-ene, reaction is the rate-limiting step of the entire process.

Mixed-Valence NpV/AnVI Molybdate Complexes with Single-Charge Outer-Sphere Cations.

Five new mixed-valence NpV/AnVI molybdates of the composition [C(NH2)3]3[(NpVO2)(NpVIO2)(MoO4)3(H2O)]·H2O (1), [C(NH2)3]3[(NpVO2)(NpVIO2)(MoO4)3(H2O)]·3H2O (2), Na3[(NpVO2)(PuVIO2)(MoO4)3(H2O)]·nH2O (3), Na6[(NpVO2)2(UVIO2)(MoO4)5]·13H2O (4), and LiNa2[(NpVO2)(NpVIO2)2(MoO4)4(H2O)]·4H2O (5) have been synthesized and structurally characterized. The coordination polyhedra of the NpV and AnVI atoms in compounds 1-5 are pentagonal bipyramids. The basis of structures 1-3 is anionic layers of the composition [(NpVO2)(AnVIO2)(MoO4)3(H2O)]n3n-. Three crystallographically independent molybdate ions are tridentate-bridging ligands. The water molecule, which is a part of the anion layer, is coordinated to the NpV atom. The anionic layers in complexes 2 and 3 have the same structure, different from 1. The basis of structure 4 is anionic layers of the composition [(NpVO2)2(UVIO2)(MoO4)5]n6n-, the structure of which differs from the structure of anionic layers in 1-3. Complex 5 has a three-dimensional (3D) structure. The spectra of all compounds in the UV-visible and IR ranges were measured and analyzed.

Thiourea as a Stabilizer of Reduced Forms of Technetium─Tc(III) and Tc(IV): Experimental and Theoretical Studies of Complexes.

This paper presents synthetic methods for the preparation of Tc(III) and Tc(IV) coordination compounds with thiourea. We have shown that the main product of the synthesis is the complex [TcTu5X]X2, (Tu = (NH2)2CS, X = Cl, Br) and not [TcTu6]Cl3·4H2O, as previously thought. Tu2[TcX6]X2·3H2O is the main technetium-containing byproduct of the reaction. All reaction products, including byproducts, were characterized by X-ray diffraction analysis. We also measured the solubility for the obtained Tc(III) complexes. This research work considers the process of thermolysis of the obtained Tc(III) complexes and shows that the presence of sulfur atoms in the coordination sphere can inhibit the process of metal formation in an argon-hydrogen medium. The analysis of nonvalent interactions in Tc(III) complexes showed that the main contribution is made by van der Waals interactions of the H···H type (40.8-42.3%) and hydrogen bonds Hal···H/H···Hal and H···S/S···H, which are 41.6-44.5% in total. As the temperature decreases, the proportion of H···H contacts and H bonds decreases, and when the halogen (Cl by Br) is replaced, the proportion of H bonds increases and the proportion of van der Waals interactions decreases.

Intramolecular Re···O Nonvalent Interactions as a Stabilizer of the Polyoxorhenate(VII).

The first polyoxorhenate(VII) compound, pyrazolium polyoxorhenate ((C4N2H5)2Re4O15), and two new rhenium(VII) and technetium(VII) salts have been synthesized and studied. The structure of Tc2O7 has been reinvestigated. The [Re4O15]2- polyoxoanion contains four Re(VII) atoms: one with an octahedral environment and three with a tetrahedral environment. Polyoxorhenate is formed in the presence of a buffering agent, pyrazole, the latter maintaining pH = 2.5 during the formation of crystals. The [Re4O15]2- polyoxoanion has novel stoichiometry and the cis-conformation, likely due to the stabilizing intramolecular nonvalence interactions. For the first time, intramolecular interactions of the Re···O, Re···µ-O, and O···O are described (previously known were only intermolecular ones). In all of the compounds, intermolecular Re···O interactions are observed, which, however, in other compounds, do not lead to the formation of polyoxometalates. The Hirshfeld surface analysis showed that the main contribution to intermolecular interactions is made by the O···H/H···O contacts, van der Waals interactions of the H···H for cations, and the O···O for anions. DFT calculations of the [Re4O15]2- geometry, compared with the crystallographic data, revealed a deviation in the angles. Mass spectroscopy of the red polyoxometalate [Tc20O68]4- was carried out for the first time. Comparison of the results of MALDI and LI for the first known polyoxometalates of the manganese subgroup made it possible to find general patterns of oligomerization for rhenium and technetium compounds. The ESI-MS and LI-MS methods applied to solution and crystals Re compounds made it possible to prove rhenium being able to form not only [Re4O15]2- but also heavier polyoxoanions.

New Preparative Approach to Purer Technetium-99 Samples-Tetramethylammonium Pertechnetate: Deep Understanding and Application of Crystal Structure, Solubility, and Its Conversion to Technetium Zero Valent Matrix.

99Tc is one of the predominant fission products of 235U and an important component of nuclear industry wastes. The long half-life and specific activity of 99Tc (212,000 y, 0.63 GBq g-1) makes Tc a hazardous material. Two principal ways were proposed for its disposal, namely, long-term storage and transmutation. Conversion to metal-like technetium matrices is highly desirable for both cases and for the second one the reasonably high Tc purity was important too. Tetramethylammonium pertechnetate (TMAP) was proposed here as a prospective precursor for matrix manufacture. It provided with very high decontamination factors from actinides (that is imperative for transmutation) by means of recrystallisation and it was based on the precise data on TMAP solubility and thermodynamics accomplished in the temperature range of 3-68 °C. The structure of solid pertechnetates were re-estimated with precise X-ray structure solution and compared to its Re and Cl analogues and tetrabutylammonium analogue as well. Differential thermal and evolved gas analysis in a flow of Ar-5% H2 gas mixture showed that the major products of thermolysis were pure metallic technetium in solid matrix, trimethylammonium, carbon dioxide, and water in gas phase. High decontamination factors have been achieved when TMAP was used as an intermediate precursor for Tc.

Influence of Substituents in a Six-Membered Chelate Ring of HG-Type Complexes Containing an N→Ru Bond on Their Stability and Catalytic Activity.

An efficient approach to the synthesis of olefin metathesis HG-type catalysts containing an N→Ru bond in a six-membered chelate ring was proposed. For the most part, these ruthenium chelates can be prepared easily and in high yields based on the interaction between 2-vinylbenzylamines and Ind II (the common precursor for Ru-complex synthesis). It was demonstrated that the increase of the steric volume of substituents attached to the nitrogen atom and in the α-position of the benzylidene fragment leads to a dramatic decrease in the stability of the target ruthenium complexes. The bulkiest iPr substituent bonded to the nitrogen atom or to the α-position does not allow the closing of the chelate cycle. N,N-Diethyl-1-(2-vinylphenyl)propan-1-amine is a limiting case; its interaction with Ind II makes it possible to isolate the corresponding ruthenium chelate in a low yield (5%). Catalytic activity of the synthesized complexes was tested in RCM reactions and compared with α-unsubstituted catalysts obtained previously. The structural peculiarities of the final ruthenium complexes were thoroughly investigated using XRD and NMR analysis, which allowed making a reliable correlation between the structure of the complexes and their catalytic properties.

Different Modes of Acid-Promoted Cyclooligomerization of 4-(4-Thiosemicarbazido)butan-2-one Hydrazone: 14-Membered versus 28-Membered Polyazamacrocycle Formation.

Unprecedented self-assembly of a novel 14-membered cyclic bis-thiosemicarbazone or/and a 28-membered cyclic tetrakis-thiosemicarbazone upon acid-promoted cyclooligomerization of 4-(4-thiosemicarbazido)butan-2-one hydrazone has been discovered. A thorough study of the influence of various factors on the direction of macrocyclization provided the optimal conditions for the highly selective formation of each of the macrocycles in excellent yields. Plausible pathways for macrocyclizations have been discussed. The macrocycle precursor was prepared by the reaction of readily available 4-isothiocyanatobutan-2-one with an excess of hydrazine.

Nucleophilic Substitution Reactions in the [B3H8]- Anion in the Presence of Lewis Acids.

As a result of our study on the interaction between the octahydrotriborate anion with nucleophiles (Nu = THF, Ph3P, Ph2P-(CH2)2-PPh2 (dppe), Ph3As, Et3N, PhNH2, C5H5N, CH3CN, Ph2CHCN)) in the presence of a wide range of Lewis acids (Ti(IV), Hf(IV), Zr(IV), Al, Cu(I), Zn, Mn(II), Co(II) halides and iodine), a number of substituted derivatives of the octahydrotriborate anion [B3H7Nu] are obtained. It is found that the use of TiCl4, AlCl3, ZrCl4, HfCl4, CuCl and iodine leads to the highest product yields. In this case, it is most likely that the reaction proceeds through the formation of an intermediate [B3H7-HMXnx], which was detected by NMR spectroscopy. The structures of [Ph3P·B3H7] and [PhNH2·B3H7] were determined by X-ray diffraction.

A 70-Year-Old Mystery in Technetium Chemistry Explained by the New Technetium Polyoxometalate [H7 O3 ]4 [Tc20 O68 ] ⋠4H2 O.

[H7 O3 ]4 [Tc20 O68 ] ⋅ 4H2 O [1] was prepared from an aqueous Tc2 O7 solution concentrated over anhydrous H2 SO4 . [Tc20 O68 ]4- is the first polyanionic species to be reported for Tc. The unit cell contains one centrosymmetric [Tc20 O68 ]4- polyanion as well as hydronium ions and water molecules. The core of the structure consists of four Tc(V)O6 octahedra that form a square Tc4 O4 ring. The four Tc(V)O6 octahedra are decorated by sixteen Tc(VII)O4 tetrahedra. Calculations show the bonding within the Tc4 O4 ring to consist of a 3-center bond formed between each neighboring pair of Tc atoms and their bridging oxygen. Calculations also indicate that a strong d→d electronic transition at 513 nm is the origin of the red color of [1]. The characterization of red HTcO4 solutions by X-ray absorption spectroscopy has complemented the description of this compound in aqueous solution. The formation mechanisms in solution, including the possible role of technetium's radioactivity in the formation of [1], are discussed.

Porphyrinylphosphonate-Based Metal-Organic Framework: Tuning Proton Conductivity by Ligand Design.

A novel metal-organic framework [Zn3 (Ni-H2 TPPP)(Ni-H4 TPPP)(Ni-H5 TPPP)⋅7(CH3 )2 NH2 ⋅DMF⋅7 H2 O] (where Ni-Hx TPPP (x=2,4,5) are partially deprotonated [5,10,15,20-tetrakis(3-(phosphonatophenyl)-porphyrinato(2-))]nickel(II) species), IPCE-2Ni, with outstanding proton conductivity (1.0×10-2  S cm-1 at 75 °C and 95 % relative humidity) has been obtained. The high concentration of free phosphonate groups and compensating dimethylammonium cations bound by hydrogen bonds in the unique crystal structure of IPCE-2Ni is a key factor responsible for the observed high proton conductivity, which is one order of magnitude higher than for the corresponding MOF based on 5,10,15,20-tetrakis(4-(phosphonatophenyl)porphyrinato(2-))]nickel(II) IPCE-1Ni and comparable with that of leaders among MOFs.

Neptunium(V) Isothiocyanate Complexes with 4'-Aryl-Substituted 2,2':6',2″-Terpyridines and N,N-Dimethylacetamide as Molecular Ligands.

New complexes of neptunyl(V) isothiocyanate with 4'-aryl-substituted 2,2':6',2″-terpyridines (Terpy) and N,N-dimethylacetamide (DMA) were obtained: [(NpO2)(4'-Ph-Terpy)(DMA)(NCS)]·DMA, [(NpO2)(4'-(4-(CF3)C6H4)-Terpy)(DMA)(NCS)]·2H2O·DMA, [(NpO2)(4'-(3-BrC6H4)-Terpy)(DMA)(NCS)]·DMA, and [(NpO2)(4'-(2-(COOH)C6H4)-Terpy)(DMA)(NCS)]·DMA. The structures of the compounds were determined with X-ray diffraction analysis. The neptunium coordination polyhedra were found to be pentagonal bipyramids with O atoms of the NpO2 groups in the apical positions and the equatorial planes formed by three N atoms of the terpyridine ligand, a N atom of the isothiocyanate anion, and an O atom of DMA. The influence of the substituents of the Ar group on the crystal structure is discussed. The IR spectra contain well-resolved bands of characteristic vibrations of all groups in the complex. The electronic absorption spectra are typical for neptunium(V) complexes and contain an intense narrow absorption band belonging to an f-f transition with a maximum of 988 nm and several long-wave satellites of lower intensity. The substituted terpyridines were shown to be efficient for the extraction of various valence forms of neptunium from the isothiocyanate solutions.

Cation-Induced Dimerization of Crown-Substituted Gallium Phthalocyanine by Complexing with Alkali Metals: The Crucial Role of a Central Metal.

The single-crystal X-ray diffraction characterization of cation-induced supramolecular assembly of the gallium(III) tetra(15-crown-5)phthalocyaninate [(HO)Ga(15C5)4Pc] (1Ga) is reported. The structures of two crystalline dimers, {[(1Ga)2Rb4]4+(iNic-)4}·10CDCl3 and {[(2Ga)2Rb4]4+(OH-)2(Piv-)2}·16CDCl3 (2Ga-[(Piv)Ga(15C5)4Pc]), as well as UV-vis and NMR studies of the soluble supramolecular dimers formed by 1Ga and K+, Rb+, and Cs+ salts are provided. In contrast to the previously reported aluminum complex where the Al-O-Al bond was formed, no µ-oxo bridge was observed between the gallium atoms in the supramolecular dimers under similar conditions, despite the fact that aluminum and gallium belong to the same group of the periodic table. The detailed investigation of the cation-induced dimers of 1Ga confirms the uniformity of their structure for all large alkali cations, where two molecules of crown-substituted gallium phthalocyaninate are 4-fold bound by K+, Rb+, or Cs+. The gallium(III) coordination sphere is labile, and the nature of the solvent during supramolecular dimerization has an effect on the axial ligand exchange: Piv- in nonpolar CHCl3 replaces the initial OH- in 1Ga, while such a process is not observed in CHCl3/CH3OH media.

Primary Amine Nucleophilic Addition to Nitrilium Closo-Dodecaborate [B12H11NCCH3]-: A Simple and Effective Route to the New BNCT Drug Design.

In the present work, a convenient and straightforward approach to the preparation of borylated amidines based on the closo-dodecaborate anion [B12H11NCCH3NHR]-, R=H, Alk, Ar was developed. This method has two stages. A nitrile derivative of the general form [B12H11NCCH3]- was obtained, using a modified technique, in the first stage. On the second stage the resulting molecular system interacted with primary amines to form the target amidine products. This approach is characterised by a simple chemical apparatus, mild conditions and high yields of the final products. The mechanism of the addition of amine to the nitrile derivative of the closo-dodecaborate anion was studied, using quantum-chemical methods. The interaction between NH3 and [B12H11NCCH3]- ammonia was chosen as an example. It was found that the structure of the transition state determines the stereo-selectivity of the process. A study of the biological properties of borylated amidine sodium salts indicated that the substances had low toxicity and could accumulate in cancer cells in significant amounts.

Fused 1,2-Diboraoxazoles Based on closo-Decaborate Anion-Novel Members of Diboroheterocycle Class.

The novel members of the 1,2-diboraoxazoles family have been obtained. In the present work, we have carried out the intramolecular ring-closure reaction of borylated iminols of general type [B10H9N=C(OH)R]- (R = Me, Et, nPr, iPr, tBu, Ph, 4-Cl-Ph). This process is conducted in mild conditions with 83-87% yields. The solid-state structures of two salts of 1,2-diboraoxazoles were additionally investigated by X-ray crystallography. In addition, the phenomena of bonding interactions in the 1,2-diboraoxazole cycles have been theoretically studied by the Quantum Theory of Atoms in Molecules analysis. Several local and integral topological properties of the electron density involved in these interactions have been computed.

Raise the anchor! Synthesis, X-ray and NMR characterization of 1,3,5-triazinanes with an axial tert-butyl group.

N-t-Bu-N',N''-Disulfonamide-1,3,5-triazinanes were synthesized and characterized by X-ray single crystal structure analysis. In the course of the X-ray structure elucidation, the first solid experimental evidence of the axial position of the tert-butyl group in unconstrained hexahydro-1,3,5-triazacyclohexanes was obtained. Dynamic low-temperature NMR analysis allowed to fully investigate a rare case of crystallization-driven unanchoring of the tert-butyl group in the chair conformation of saturated six-membered cycles. DFT calculations show that the use of explicit solvent molecules is necessary to explain the equatorial position of the t-Bu group in solution. Otherwise, the axial conformer is the thermodynamically stable isomer.

Application of New Efficient Hoveyda-Grubbs Catalysts Comprising an N→Ru Coordinate Bond in a Six-Membered Ring for the Synthesis of Natural Product-Like Cyclopenta[b]furo[2,3-c]pyrroles.

The ring rearrangement metathesis (RRM) of a trans-cis diastereomer mixture of methyl 3-allyl-3a,6-epoxyisoindole-7-carboxylates derived from cheap, accessible and renewable furan-based precursors in the presence of a new class of Hoveyda-Grubbs-type catalysts, comprising an N→Ru coordinate bond in a six-membered ring, results in the difficult-to-obtain natural product-like cyclopenta[b]furo[2,3-c]pyrroles. In this process, only one diastereomer with a trans-arrangement of the 3-allyl fragment relative to the 3a,6-epoxy bridge enters into the rearrangement, while the cis-isomers polymerize almost completely under the same conditions. The tested catalysts are active in the temperature range from 60 to 120 °C at a concentration of 0.5 mol % and provide better yields of the target tricycles compared to the most popular commercially available second-generation Hoveyda-Grubbs catalyst. The diastereoselectivity of the intramolecular Diels-Alder reaction furan (IMDAF) reaction between starting 1-(furan-2-yl)but-3-en-1-amines and maleic anhydride, leading to 3a,6-epoxyisoindole-7-carboxylates, was studied as well.

Insight of the Metal-Ligand Interaction in f-Element Complexes by Paramagnetic NMR Spectroscopy.

The magnetic properties of LnIII and AnIII complexes formed with dipicolinate ligands have been studied by NMR spectroscopy. To know precisely the geometries of these complexes, a crystallographic study by single-crystal X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) in solution was performed. Several methods to separate the paramagnetic shifts observed in the NMR spectra were applied to these complexes. Methods using a number of nuclei of the dipicolinate ligands revealed an abrupt change in the geometries of the complexes and a metal-ligand interaction in the middle of the lanthanide series. A study of the variation of the paramagnetic shifts with temperature demonstrated that higher-order terms of the dipolar and contact contributions are required, especially for the lightest LnIII and almost all the studied AnIII . Bleaney's parameters a and C a D relating to the contact and dipolar terms, respectively, were deduced from experimental data and compared with the results of ab initio calculations. Quite a good agreement was found for the temperature dependencies of a and C a D . However, the C a D values obtained from cation magnetic anisotropy calculations showed some discrepancies with the values derived from Bleaney's equation defined for LnIII . Other parameters, such as the crystal field parameter and the hyperfine constants Fi obtained from the experimental data of the [An(ethyl-dpa)3 ]3- complexes (ethyl-dpa=4-ethyl-2,6-dipicolinic acid), are at odds with the assumptions underlying Bleaney's theory.

Highly Proton-Conductive Zinc Metal-Organic Framework Based On Nickel(II) Porphyrinylphosphonate.

The design of new solid-state proton-conducting materials is a great challenge for chemistry and materials science. Herein, a new anionic porphyrinylphosphonate-based MOF (IPCE-1Ni), which involves dimethylammonium (DMA) cations for charge compensation, is reported. As a result of its unique structure, IPCE-1Ni exhibits one of the highest value of the proton conductivity among reported proton-conducting MOF materials based on porphyrins (1.55×10-3  S cm-1 at 75 °C and 80 % relative humidity).

Peculiarities of the Supramolecular Assembly of Tetraethylammonium and 3-Bromopropionate Ions in Uranyl, Neptunyl, and Plutonyl Coordination Compounds.

Synthesis and X-ray diffraction studies of {N(C2H5)4}[AnO2(C2H4BrCOO)3] [An = U (I), Np (II), or Pu (III)] and C2H4BrCOOH (IV), where C2H4BrCOO- is an anion of the 3-bromopropionic acid, are reported. The isostructural coordination compounds I-III contain mononuclear anionic complexes [AnO2(C2H4BrCOO)3]- belonging to the crystal chemical group AB013 (A = AnO22+; B01 = C2H4BrCOO-). In the crystal structure of IV, the C2H4BrCOOH molecules are hydrogen bonded into centrosymmetric dimers R22(8). Using the method of molecular Voronoi-Dirichlet (VD) polyhedra, the features of intermolecular interactions in crystals of I-IV are discussed in support of the results of IR and UV spectroscopy experiments. Actinide contraction in I-III manifests itself in a regular reduction of the average length of the axial and equatorial bonds in hexagonal bipyramids AnO8, in an increase in νas(AnO22+) wavenumbers, and in a simultaneous decrease in the volume and sphericity degree of VD polyhedra of An atoms in the U-Np-Pu series. The title compounds represent an interesting architecture, where 3-bromopropionate ions penetrate through the square 44 net of tetraethylammonium ions and thus bind adjacent nets via the "locking effect".