Electrophilic Behavior of the "Nucleophilic" Pyramidane: Reactivity of Ge-Pyramidane towards Organolithium Reagents.

The particular reactivity of the recently discovered class of the main group element polyhedral clusters, pyramidanes, remains largely unexplored. In this communication, we report the reaction of the germapyramidane with tert-butyllithium leading to the rather unusual organogermanium compound [Li+(thf)2]⋅2-, as the product of the formal insertion of a Ge-apex into the C-Li bond. This reactivity mode exemplifies unusual electrophilic behaviour of a pyramidane, which is a priori considered as a nucleophilic reagent. Being highly reactive, [Li+(thf)2]⋅2- readily undergoes reactions with electrophiles (MeI, EtBr), initially forming intermediate germahousenes, which isomerize to the thermodynamically more favourable germoles.

Direct Conversion of Low-Concentration CO2 into N-Aryl and N-Alkyl Carbamic Acid Esters Using Tetramethyl Orthosilicate with Amidines as a CO2 Capture Agent and a Catalyst.

Herein, we report the direct conversion of low-concentration CO2 (15 vol %), equivalent to the CO2 concentration in the exhaust gas from a thermal power station, into carbamic acid esters (CAEs), which are precursors for pharmaceuticals, agrochemicals, and isocyanates. The reaction was performed using Si(OMe)4 as a nonmetallic regenerable reagent and 1,8-diazabicyclo[5.4.0]undec-7-ene as a CO2 capture agent and catalyst. This reaction system does not require the addition of metal complex catalysts or metal salt additives and is therefore simpler than our previously reported reaction system involving Ti(OR)4 and a Zn(II) catalyst. A variety of N-aryl, N-alkyl, and bis CAEs (precursors of polyurethane raw materials) were obtained in moderate to high yields (45-77% for 6 examples, 84-89% for 7 examples). In addition, bis CAEs were successfully synthesized from simulated exhaust gas containing impurities such as SO2, NO2, and CO or on a gram scale. We believe that this method can eliminate the use of toxic phosgene as the raw material for isocyanate production and mitigate CO2 emissions.

Bidentate Disilicate Framework for Bis-Grafted Surface Species.

Recent advances in surface organometallic chemistry have enabled the detailed characterization of the surface species in single-site heterogeneous catalysts. However, the selective formation of bis-grafted surface species remains challenging because of the heterogeneity of the supporting surface. Herein, we introduce a metal complex bearing bidentate disilicate ligands, -OSi(Ot Bu)2 OSi(Ot Bu)2 O-, as a molecular precursor, which has a silicate framework adjacent to the metal (Pt) center. The grafting of the precursors on silica supports (MCM-41 and CARiACT Q10) proceeded through a substitution reaction on the silicon atoms of the disilicate ligand, which was verified by the detection of isobutene and t BuOH as the elimination products, to selectively yield bis-grafted surface species. The chemical structure of the surface species was characterized by solid-state NMR, and the chemical shift values of the ancillary ligands and 195 Pt nuclei suggested that the bidentate coordination sphere was maintained following grafting.

N-Aryl and N-Alkyl Carbamates from 1 Atmosphere of CO2.

We have successfully isolated and characterized the zinc carbamate complex (phen)Zn(OAc)(OC(=O)NHPh) (1; phen=1,10-phenanthroline), formed as an intermediate during the Zn(OAc)2 /phen-catalyzed synthesis of organic carbamates from CO2 , amines, and the reusable reactant Si(OMe)4 . Density functional theory calculations revealed that the direct reaction of 1 with Si(OMe)4 proceeds via a five-coordinate silicon intermediate, forming organic carbamates. Based on these results, the catalytic system was improved by using Si(OMe)4 as the reaction solvent and additives like KOMe and KF, which promote the formation of the five-coordinated silicon species. This sustainable and effective method can be used to synthesize various N-aryl and N-alkyl carbamates, including industrially important polyurethane raw materials, starting from CO2 under atmospheric pressure.

Wet and Dry Processes for the Selective Transformation of Phosphonates to Phosphonic Acids Catalyzed by Brønsted Acids.

A "wet" process and two "dry" processes for converting phosphonate esters to phosphonic acids catalyzed by a Brønsted acid have been developed. Thus, in the presence of water, a range of alkyl-, alkenyl-, and aryl-substituted phosphonates can be generally hydrolyzed to the corresponding phosphonic acids in good yields catalyzed by trifluoromethyl sulfonic acid (TfOH) at 140 °C (the wet process). On the other hand, with specific substituents of the phosphonate esters, the conversion to the corresponding phosphonic acids can be achieved under milder conditions in the absence of water (the dry process). Thus, the conversion of dibenzyl phosphonates to the corresponding phosphonic acids took place smoothly at 80 °C in toluene or benzene in high yields. Moreover, selective conversion of benzyl phosphonates RP(O)(OR')(OBn) to the corresponding mono phosphonic acids RP(O)(OR')(OH) can also be achieved under the reaction conditions. The dealkylation via the generation of isobutene of di-tert-butyl phosphonate, and the related catalysis by TfOH took place even at room temperature to give the corresponding phosphonic acids in good to high yields. Nafion also shows high catalytic activity for these reactions. By using Nafion as the catalyst, phosphonic acids could be easily prepared on a large scale via a simple process.

Regioselective Diels-Alder reaction to open-cage ketolactam derivatives of C60.

Open-cage ketolactam fullerenes reacted with dienes on the rim of the orifice both regio- and stereoselectively. Unequivocal evidence for the structure of the Diels-Alder adduct was provided by 2D INADEQUATE 13C NMR studies on 13C enriched material, as well as via DFT-GIAO calculations. The theoretical calculations successfully model the regioselective and the endo stereoselective reaction, predicting molecular orbital control along with a repulsive steric interaction between the substituents on the nitrogen atom and those on the diene.

Dialkyl Carbonate Synthesis Using Atmospheric Pressure of CO2.

Dialkyl carbonates (DRCs) are valuable compounds widely used in the industry. The synthesis of DRC from CO2 has attracted interest as an alternative to the current method, which uses phosgene. However, the reported approaches for DRC synthesis from CO2 requires high-pressure and high-concentration CO2, resulting in elevated costs associated with CO2 purification and manufacturing facilities. In this report, we present an environmentally friendly method for producing DRC from low-concentration and low-pressure CO2 via a dehydration condensation approach without the use of halogenated alkylating agents. This method involves the formation of monoalkyl carbonate [BASE-H][ROC(O)O] using a strong organic base and alcohols, tetraalkyl orthosilicates as dehydrating agents, and CeO2 as the catalyst. Using the method, 39 and 30% of diethyl carbonate yields were accomplished with only 100 and 15 vol % CO2 (CO2/N2 = 15:85) gas bubbling at atmospheric pressure, even under reaction conditions with no large excess of either CO2, alcohol, or dehydration agent.

Design and assessment of an energy self-supply process producing tetraethyl orthosilicate using rice husk.

Combusting rice husk (RH) generates energy and rice husk ash (RHA) containing high amount of silica. Recent studies showed RHA can directly react with ethanol for producing tetraethyl orthosilicate (TEOS), an important substance for different industries. Nevertheless, this process requires an intensive energy supply. This study aims to design and evaluate an energy self-supply process producing TEOS using RH for feasibility. A process simulator was used to design the target process. The simulation results revealed that RH combustion can completely meet the RHA and high energy demands of TEOS production. The economic and environmental benefits were thoroughly evaluated and compared with processes using conventional raw materials (i.e., Simg and silica). The evaluation results showed that using RH for TEOS production could reduce CO2 emissions substantially. Large economic benefit was gained when renewable electricity was co-generated and sold to the power grid as a surplus.

Synthesis of organic carbamates as polyurethane raw materials from CO2: the quest for metal alkoxides as regenerable reagents.

It is well known that the utilization of carbon dioxide (CO2) for chemical materials is attracting research attention from the viewpoint of the carbon cycle. To contribute to the reduction of CO2 emission through such CO2 utilization reactions and counteract global climate change, the target compounds should be core chemical products that are distributed in large quantities and used for a long time. One such synthetic target is isocyanates that are used as raw materials for the production of polyurethanes, which are versatile polymeric materials with a service life of approximately 10 years. However, since direct synthesis of isocyanate from CO2 is quite difficult due to equilibrium constraints, a method via the use of its alcohol adduct, organic carbamate, as a precursor has been proposed. In this Perspective, we present regenerative metal alkoxide reactants, such as tin alkoxide, titanium alkoxide, and alkoxysilane, as environmentally benign reactants for the synthesis of organic carbamates from CO2. We also present a practical and environmentally friendly method for the highly efficient synthesis of various organic carbamates, including industrially important diisocyanate precursors, from 1 atm CO2 using alkoxysilanes. Furthermore, prospects for the practical application of these carbamate synthesis reactions are also discussed.

Controlled Growth of Platinum Nanoparticles on Amorphous Silica from Grafted Pt-Disilicate Complexes.

Supported platinum nanoparticles are currently the most functional catalysts applied in commercial chemical processes. Although investigations have been performed to improve the dispersion and thermal stability of Pt particles, it is challenging to apply amorphous silica supports to these systems owing to various Pt species derived from the non-uniform surface structure of the amorphous support. Herein, we report the synthesis and characterization of amorphous silica-supported Pt nanoparticles from (cod)Pt-disilicate complex (cod = 1,5-cyclooctadiene), which forms bis-grafted surface Pt species regardless of surface heterogeneity. The synthesized Pt nanoparticles were highly dispersible and had higher hydrogenation activity than those prepared by the impregnation method, irrespective of the calcination and reduction temperatures. The high catalytic activity of the catalyst prepared at low temperatures (such as 150 °C) was attributed to the formation of Pt nanoparticles triggered by the reduction of cod ligands under H2 conditions, whereas that of the catalyst prepared at high temperatures (up to 450 °C) was due to the modification of the SiO2 surface by grafting of the (cod)Pt-disilicate complex.

Fluoride Ion-Initiated Decarboxylation of Silyl Alkynoates to Alkynylsilanes.

This communication describes the development of a metal-free catalytic decarboxylation of silyl alkynoates to alkynylsilanes. Treatment of a silyl alkynoate with a catalytic amount of tetrabutylammonium difluorotriphenylsilicate (TBAT) in N,N-dimethylformamide at 150 °C resulted in decarboxylation to give the corresponding alkynylsilane in good to excellent yield (75 → 95%). The TBAT system was applicable to the decarboxylation of sterically demanding silyl alkynoates such as tert-butyldiphenylsilyl 3-phenylpropiolate. Mechanistic studies revealed that the tetrabutylammonium alkynoate derived from TBAT and the silyl alkynoate act as a catalyst for the decarboxylation.

From SiO2 to Alkoxysilanes for the Synthesis of Useful Chemicals.

The transformation of silica (SiO2) to useful chemicals is difficult to explore because of the strength of the Si-O bond and thermodynamic stability of the SiO2 structure. The direct formation of alkoxysilanes from SiO2 has been explored as an alternative to the carbothermal reduction (1900 °C) of SiO2 to metallic silicon (Simet) followed by treatment with alcohols. The base-catalyzed depolymerization of SiO2 with diols and monoalcohols afforded cyclic silicon alkoxides and tetraalkoxysilanes, respectively. SiO2 can also be converted to alkoxysilanes in the presence of organic carbonates, such as dimethyl carbonate. Alkoxysilanes can be further converted to useful chemicals, such as carbamates, organic carbonates, and chlorosilanes. An interesting and highly efficient pathway to the direct conversion of SiO2 to alkoxysilanes has been discussed in detail along with the corresponding economic and environmental implications. The thermodynamic and kinetic aspects of SiO2 transformations in the presence of alcohols are also discussed.

One-pot catalytic synthesis of urea derivatives from alkyl ammonium carbamates using low concentrations of CO2.

To reduce anthropogenic carbon dioxide (CO2) emissions, it is desirable to develop reactions that can efficiently convert low concentrations of CO2, present in exhaust gases and ambient air, into industrially important chemicals, without involving any expensive separation, concentration, compression, and purification processes. Here, we present an efficient method for synthesizing urea derivatives from alkyl ammonium carbamates. The carbamates can be easily obtained from low concentrations of CO2 as present in ambient air or simulated exhaust gas. Reaction of alkyl ammonium carbamates with 1,3-dimethyl-2-imidazolidinone solvent in the presence of a titanium complex catalyst inside a sealed vessel produces urea derivatives in high yields. This reaction is suitable for synthesizing ethylene urea, an industrially important chemical, as well as various cyclic and acyclic urea derivatives. Using this methodology, we also show the synthesis of urea derivatives directly from low concentration of CO2 sources in a one-pot manner.

Sustainable Catalytic Synthesis of Diethyl Carbonate.

New sustainable approaches should be developed to overcome equilibrium limitation of dialkyl carbonate synthesis from CO2 and alcohols. Using tetraethyl orthosilicate (TEOS) and CO2 with Zr catalysts, we report the first example of sustainable catalytic synthesis of diethyl carbonate (DEC). The disiloxane byproduct can be reverted to TEOS. Under the same conditions, DEC can be synthesized using a wide range of alkoxysilane substrates by investigating the effects of the number of ethoxy substituent in alkoxysilane substrates, alkyl chain, and unsaturated moiety on the fundamental property of this reaction. Mechanistic insights obtained by kinetic studies, labeling experiments, and spectroscopic investigations reveal that DEC is generated via nucleophilic ethoxylation of a CO2 -inserted Zr catalyst and catalyst regeneration by TEOS. The unprecedented transformation offers a new approach toward a cleaner route for DEC synthesis using recyclable alkoxysilane.

Synthesis and Structure of Multinuclear Pd(II) Complexes Bridged by Phosphide or Azide Ligands.

The synthesis and structure of phosphide- and azide-bridged multinuclear Pd(II) complexes bearing phosphine ligands [PdX(µ-X')(PR3)] n (X = Cl and N3; X' = PR2 ' and N3; n = 2 and 4) are reported. The oxidative addition of R2 'PCl to Pd(PMe3)2 furnished the phosphide-bridged dinuclear Pd(II) complexes [PdCl(µ-PR2 ')(PMe3)]2 [R' = i Pr (1a) and Cy (1b)]. However, the oxidative addition of (o-tolyl)2PCl to Pd(PMe3)2 produced a nonbridged mononuclear Pd(II) complex with the bis(o-tolyl)phosphinic ligand, trans-[Pd(PMe3)2{P(O)(o-tolyl)2}] (2), via oxidation of the phosphinyl ligand. The reaction of the chloride-bridged dinuclear Pd(II) complexes [PdCl(µ-Cl)(PR3)]2 [PR3 = PEt3 (3a) and PPhMe2 (3b)] with NaN3 afforded the azide-bridged dinuclear and tetranuclear Pd(II) complexes [Pd(N3)(µ-N3)(PEt3)]2 (4) and [Pd(N3)(µ-N3)(PPhMe2)]4 (5). Comparisons of the X-ray structures of 4 and 5 show that the square-planar molecular geometry of the Pd(II) centers of 4 are more distorted than those of 5. Density functional theory calculations suggest that the tetranuclear eight-membered ring structure like 5 is more stable than the dinuclear four-membered ring structure like 4 in the gas phase in both PEt3 and PPhMe2 systems. However, because the relative energy difference between the four-membered and eight-membered ring structures is small in the PEt3 system with smaller steric hindrance compared with PPhMe2, it is assumed that this difference is compensated by the crystal packing energy, and the dinuclear four-membered ring complex 4 is actually obtained.

A Simple Zinc Catalyst for Carbamate Synthesis Directly from CO2.

Several zinc salts were employed as catalysts for the synthesis of carbamates directly from aromatic amines, CO2 , and silicate esters. Zn(OAc)2 offered the best performance among the salts tested. The addition of an N-donor ligand such as 1,10-phenanthroline increased the yield. The best catalytic performance of Zn(OAc)2 can be explained by carboxylate-assisted proton activation. The interaction between the substrate and the catalyst can be observed by chemical shifts in 1 H and 15 N NMR spectra. Isocyanate was a key intermediate, which was generated from amine and CO2 . Silicate ester was finally converted to siloxane, which was determined by 29 Si NMR. The commercially available catalyst system could be reused. The yield of isolated carbamate could reach up to 96 % with various substrates, and the catalytic reaction was amine-selective in the presence of other functional groups.

Halogen-Free Synthesis of Carbamates from CO2 and Amines Using Titanium Alkoxides.

A direct synthesis of carbamates from amines and carbon dioxide in the presence of Ti(OR)4 (R=nBu (1), Me (2), Et (3), nPr (4)) was investigated. Aniline was reacted with titanium n-butoxide (1) in the presence of carbon dioxide (5 MPa) to give the corresponding n-butyl N-phenylcarbamate (BPC) in nearly quantitative yield (99 %) within 20 min. Furthermore, 1 could be regenerated upon reaction with n-butanol during water removal. The recovered 1 could then be reused in a subsequent reaction.

Synthesis of cyclic sulfites from epoxides and sulfur dioxide with silica-immobilized homogeneous catalysts.

Quaternary ammonium- and amino-functionalized silica catalysts have been prepared for the selective synthesis of cyclic sulfites from epoxides and sulfur dioxide, demonstrating the effects of immobilizing the homogeneous catalysts on silica. The cycloaddition of sulfur dioxide to various epoxides was conducted under solvent-free conditions at 100 °C. The quaternary ammonium- and amino-functionalized silica catalysts produced cyclic sulfites in high yields (79-96 %) that are comparable to those produced by the homogeneous catalysts. The functionalized silica catalysts could be separated from the product solution by filtration, thereby avoiding the catalytic decomposition of the cyclic sulfite products upon distillation of the product solution. Heterogenization of a homogeneous catalyst by immobilization can, therefore, improve the efficiency of the purification of crude reaction products. Despite a decrease in catalytic activity after each recycling step, the heterogeneous pyridine-functionalized silica catalyst provided high yields after as many as five recycling processes.

The first halogen-substituted cyclotrigermenes: a unique halogen walk over the three-membered ring skeleton and facial stereoselectivity in the Diels-Alder reaction.

Dark red crystals of the halogen-substituted cyclotrigermenes [(tBu3Si)3Ge3X; X = Cl, Br, I] were obtained in good yields by the reaction of [(tBu3Si)3Ge3]+.TTFPB- (TTFPB- = tetrakis(2,3,5,6-tetrafluorophenyl)borate) with potassium halides (KCl, KBr, or KI) in diethyl ether. The crystal structures of the halogen-substituted cyclotrigermenes reveal a cis-bent Ge=Ge double bond, caused by the introduction of the electronegative halogen atom on the sp3 germanium atom of cyclotrigermene. In solution, an intramolecular halogen migration over the three-membered ring skeleton was observed. Facial stereoselectivity in the Diels-Alder reaction of new cyclotrigermenes with 2,3-dimethyl-1,3-butadiene is also reported.