1,3-Diphosphapropenes for novel chemistry of metal complexes

2-Methyl-3,3-diphenyl-1-(2,4,6-tri-t-butylphenyl)-1,3-diphosphapropene was obtained as a chelate ligand for palladium(II) and platinum(II) complexes. Sulfurization of 2-methyl-1,3-diphosphapropene mainly gave 3-thioxo-1,3-diphosphapropene which bears a PC-PS skeleton and was used as a ligand of transition-metal complexes. A doubly-sulfurized product of the 1,3-diphosphapropene, 1,3-dithioxo-1,3-diphosphapropene, was isolated and characterized. The palladium(II) complexes containing the ligated 1,3-diphosphapropenes were used for catalytic reactions such as cross-couplings and direct conversion of allyl alcohol to allylaniline.     

Catalysis of hydrosilylation of carbon-carbon multiple bonds: Recent progress

Recent progress in the catalytic hydrosilylation of organic and organosilicon compounds containing carbon-carbon multiple bonds is reviewed. Related to this, dehydrogenative silylation is also discussed. During the last decade new hydrosilylation catalysts, predominantly homogenous and heterogenous transition methal complexes, have been developed. These catalysts offer not only increased efficiency and turnover rate but also improved regioselectivity and stereoselectivity; moreover, there has been development in the mechanistic rationale behind these improvements. Application and extension of these basic chemical advances are found in many areas including polyorganosiloxane curing, hydrosilylation polymerization, polysiloxane functionalization, and silicon-containing dendrimer development.     

Photoredox processes in coordination compounds

Transition metal complexes display a number of charge-transfer bands in the absorption spectra. Optical excitation of the metal complexes produces a variety of products depending upon the nature of the excited state. Cobalt (III) ammine complexes on excitation in the CTTM bands produce cobalt(II) and oxidised ligand. Ruthenium(II) complexes on excitation in the cm. band leads to the oxidation of the metal centre. In certain reactions participation of the solvent in the primary photoredox reactions has also been reported. In recent years extensive investigations have been undertaken to utilize the photoredox systems of coordination compounds to convert solar energy to electricity or hydrogen.     

Cyclobutadiene cobalt complexes as catalysts for insertion of diazo compounds into X–H bonds

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Topological aspects of metals in carbon cages: Analogies with organometallic chemistry

Metals can interact with carbon cages in the following ways: (1) stable carbon cages (i.e., fullerenes) function as electronegative olefins in their exohedral η₂ bonding to transition metals; (2) endohedral metallofullerenes with a highly electropositive lanthanide (Ln) inside the carbon cage can be considered to be ionic with lanthanide cations, Ln³⁺, and fullerene anions; (3) fullerenes too small for independent existence can be stabilized by internal covalent bonding to an endohedral metal atom using the central carbon atoms of pentagon triplets,i.e triquinacene, units, in complexes such as M@C₂₈ (M=Ti, Zr, Hf, and U), derived from the tetrahedral fullerene C₂₈; (4) metal atoms can occur as vertices of binary mixed metal-carbon cages in both early transition metal complexes of the types M₁₄C₁₃, M₈C₁₂, and M₁₃C₂₂ (e.g., M=Ti) and copper-carbon cages of the types Cu_2n +1C_2n ⁺ (n≤10), Cu₇C₈ ⁺, Cu₉C₁₀ ⁺ and Cu₁₂C₁₂ ⁺. The presence of metal atoms as vertices of carbon cages changes radically their stoichiometries and thus their structures. Thus, early transition metals form cages such as Ti₁₄C₁₃ assumed to have titanium atoms at the vertices and face midpoints of a 3×3×3 cube and carbon atoms at the edge midpoints and center of the cube and Ti₁₃C₂₂ assumed to have titanium atoms at the edge midpoints and center of a 3×3×3 cube as well as C₂ units and carbon atoms at the vertices and face midpoints, respectively, of the cube. Elimination of the face metal atoms from the Ti₁₄C₁₃ structure as well as the center carbon atom, which has been achieved experimentally by photofragmentation, leads to the Ti₈C₁₂ cluster. The structure of this cluster is based on a tetracapped tetrahedron withT _d symmetry with two distinct quartets of titanium atoms, six distinct C₂ pairs, and 36 direct Ti−C interactions. The copper-carbon cages of various stoichiometries are suggested to have prismatic, antiprismatic, or cuboctahedral structures in which the electronic configurations of the copper atoms approach the favored 18-electron rare gas configuration. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 862–869, May, 1998.     

Conformational changes of DNA molecules in interactions with bioactive compounds. II. DNA complexes with coordination compounds of cobalt and ruthenium

A comparative analysis is made of the character of conformational changes of the DNA molecule in its interaction with coordination compounds of cobalt and ruthenium with different ligand sets in the coordination sphere of the ion. It is shown that during complexation global conformational changes of DNA (e.g., the reduction of its volume) practically do not depend on the location and on the binding mode of the complex ion, but are primarily determined by its charge, whereas local conformational changes of the macromolecule are very sensitive to the type of the complex being formed, as indicated by the change of spectral properties of DNA. An assessment of sizes of the particles that are formed as a result of DNA condensation due to its binding with trivalent ions of cobalt and ruthenium was performed with the use of dynamic light scattering.     

A double heteroatom Mitsunobu coupling with amino hydroxybenzoic acids on solid phase: a novel application of the Mitsunobu reaction to form dendron building blocks

A new highly efficient double heteroatom Mitsunobu coupling with amino hydroxybenzoic acids on solid phase is described. The synthetic routes reported in this work are general and applicable for the preparation of diverse building blocks, controlling protection, arm length, chirality, and peripheral functional groups. These novel units can form unusual dendritic architectures, which could be incorporated into specific complex structures, expanding the scope of dendrimer science.     

Review: recent advances in the chemistry of metal chelate monomers

This review summarizes recent advances in the chemistry of metal chelate monomers. Depending on the character of bonding of the metal to the chelating fragment, metal chelate monomers are divided into four main types: molecular metal chelates, intracomplex compounds, macrocyclic complexes, and polynuclear metal chelates. The synthetic methodologies for preparing metal chelate monomers are systematized. Special attention is paid to the effect of a metal on both the polymerization transformations of the metal chelate monomers and properties of the products formed. The bibliography includes papers published after 2010.     

Design,synthesis and crystallographic study of novel indole‐based cyano derivatives as key building blocks for heteropolycyclic compounds of major complexity

A four‐stage reaction sequence has been designed and developed for the synthesis of highly functionalized enolate esters as key building blocks for the synthesis of novel heteropolycyclic compounds of potential pharmaceutical value. The sequence starts with simple commercially available indoles and proceeds via 3‐(indol‐3‐yl)‐3‐oxopropanenitriles, which react with 2‐bromobenzaldehyde to form the corresponding chalcones; these are readily reduced to dihydrochalcones, which are in turn acylated to form the enolate esters. The compounds in this sequence have been characterized by IR and ¹H and ¹³C NMR spectroscopy, by mass spectrometry and by elemental analysis. The molecular and supramolecular structures are reported for representative examples, namely (E )‐3‐(2‐bromophenyl)‐2‐(1‐methyl‐1H‐indole‐3‐carbonyl)acrylonitrile, C₁₉H₁₃BrN₂O, (Ib ), (2RS )‐2‐(2‐bromobenzyl)‐3‐(1‐methyl‐1H‐indol‐3‐yl)‐3‐oxopropanenitrile, C₁₉H₁₅BrN₂O, (IIb ), and (2RS )‐3‐(1‐benzyl‐1H‐indol‐3‐yl)‐2‐(2‐bromobenzyl)‐3‐oxopropanenitrile, C₂₅H₁₉BrN₂O, (IIc ), the latter two of which crystallize with Z ′ = 2, and (E )‐1‐(1‐acetyl‐1H‐indol‐3‐yl)‐3‐(2‐bromophenyl)‐2‐cyanoprop‐1‐en‐1‐yl acetate, C₂₂H₁₇BrN₂O, (III), and (E )‐1‐(1‐benzyl‐1H‐indol‐3‐yl)‐3‐(2‐bromophenyl)‐2‐cyanoprop‐1‐en‐1‐yl benzoate, C₃₂H₂₃BrN₂O, (IV). The structure of the related chalcone (E )‐2‐benzoyl‐3‐(2‐bromophenyl)prop‐2‐enenitrile, (V), has been redetermined at 100 K, where it is monoclinic, as opposed to the triclinic form reported at ambient temperature.     

New strategies in the synthesis of regioselectively trifluoromethyl- and trifluoromethoxy-substituted arenes as building blocks for biologically active molecules

Regioisomerically pure trifluoromethyl- and trifluoromethoxy-substituted aromatic and heteroaromatic aldehydes and carboxylic acids are valuable building blocks for the synthesis of biologically active molecules. They have been prepared by employing modern organometallic methods. On this basis, a novel access to 2,3-dihydro-5-(trifluoromethoxy)indole was developed which represents an intriguing example of how organometallic and radical chemistry can fecundate each other.     

Beneficial effect of water as second solvent in ionic liquid biphasic catalytic hydrogenations

When reactions take place in ionic liquids, a solvent is normally used to extract the products after reaction. It is reported here how the presence of the solvent during the reaction already can seriously improve the catalytic performance. Above all, employing water as the added solvent enhanced the catalytic activities significantly, ascribed to the creation of a well mixed ‘emulsion-like’ system. The reductions of methyl 2-acetamidoacrylate with Rh-EtDuPHOS and of 2-cyclohexen-1-one with Wilkinson’s catalyst in bmimPF₆ were thus successfully performed in the presence of water. The complexes were easily recycled and Rh-EtDuPHOS was even no longer air sensitive.     

ⅥB族金属叁键有机化合物的研究进展

本文对一类重要的ⅥB族金属叁键化合物R_2M_2(CO)_4(R为环戊二烯基及类环戊二烯基)近年来的研究成果进行了综述,综述重点是这类化合物的官能团M≡M参键的化学活性,全文包括R_2M_2(CO)_4的合成及结构,M≡M叁键与亲核试剂、与碳-碳重键,与氧或与金属羰基物等试剂的反应及其应用。     

Catching gaseous SO2 in cone-type lanthanide complexes: an unexpected coordination mode for SO2 in f-element chemistry

Easy come, easy go: the first molecular SO(2) complexes of the lanthanides (Ln=Sm, Eu) have been prepared. The compounds can reversibly coordinate gaseous SO(2). Concomitant with the addition and removal of SO(2), the color of the complexes changes reversibly. The structures of the SO(2) compounds could be confirmed in solution and in the solid state.     

Studies in pyrimidine-annulated heterocycles: unusual formation of spiroheterocyclic compounds from acid catalyzed reaction of enol ether

A number of spiroheterocycles are synthesized in moderate yield by treating 5-aryloxymethylene-6,7,8-trihydropyrido[2,3-d]pyrimidines-2,4(1H,3H)diones with H₂SO₄ in chloroform-methanol-water. These spiroheterocycles are also regioselectively synthesized by tri-n-butyltin hydride induced radical cyclization of 5-(o-bromoaryloxymethylene)-6,7,8-trihydropyrido[2,3-d]pyrimidines-2,4(1H,3H)diones.     

Investigation of the typical triangular structure B3 in boron chemistry: insight into bare all-boron clusters used as ligands or building blocks

Even though boron clusters are quite significant, bare boron clusters as ligands in chemical compounds are still unknown. Triangular B(3) is a key constituent of all-boron clusters and widely applied in the boron compounds. As a basic step toward understanding the assembly and stabilization of bare all-boron clusters and the possibility of their fusion during the cluster-assembly process, we made the first attempt to assemble the smallest bare all-boron unit B(3)-. Both the "homo-decked sandwich" and "hetero-decked sandwich" schemes were applied to the assembly of B(3)- at the B3LYP/6-311++G(d, p) level. For all the considered alkali- and alkaline earth metals, B(3)- can only be assembled in "hetero-decked sandwich" scheme (e.g., CpMB(3)(q-)) so as to avoid cluster fusion, whereas it cannot be assembled in the traditional "homo-decked sandwich" scheme (B(3)MB(3)(q-)) because of thermodynamic and kinetic instability. Various assembled species in extended frameworks are designed. In particular, the dimerization of the hetero-decked sandwich-like CpMB(3)(q-) could lead to a new type of antiaromatic triple-decker sandwich-like complexes CpMB(6)Cp(2q-) that contain the all-boron antiaromatic unit B(6)(2-). Our work supports the experimental identification of the B(6)(2-) anion (with M+ counterions) in a photoelectron spectroscopy study. Additionally, the electronic and structural properties of B(3)- are well conserved during cluster-assembly, characteristic of a "superatom" feature. Our results are expected to be helpful for understanding the assembly and stabilization of bare all-boron cluster chemistry. Also, our work should give insight toward designing and understanding bare boron clusters as potential new ligands for coordination chemistry and as new building blocks for materials science. Interestingly, our results should provide hints to embellish, functionalize, isolate, and protect bare all-boron clusters.