Silicon Analogues Research Articles

Annulated 1,4-Disilabenzene-1,4-diide and Dihydrogen Splitting.

The isolation of silicon analogues of phenyl anions such as (C6H5)- and (C6H4)2- is challenging owing to their extremely high reactivity associated with their silylene character and weak C-Si π-interaction. Herein, we report the first annulated 1,4-disilabenzene-1,4-diide compound [(ADC)Si]2 (5) based on anionic dicarbene (ADC) scaffolds (ADC = PhC{N(Dipp)C}2; Dipp = 2,6-iPr2C6H3) as a green-yellow crystalline solid. Compound 5 is prepared by KC8 reduction of the Si(IV) chloride [(ADC)SiCl3]2 (3) or the cyclic bis-chlorosilylene [(ADC)SiCl]2 (4), which are also prepared for the first time. 5 is a neutral molecule, and each of the two-coordinated Si(I) atoms has a lone pair and an unpaired electron. Experimental and theoretical data indicate delocalization of the silicon unpaired electrons, resulting in a 6π-electron C4Si2 ring in 5. The diradical character (y) for 5 amounts to 15%. At room temperature, 5 readily reacts with dihydrogen (H2) to form the elusive bis-hydridosilylenes [(ADC)SiH]2 (Z)-6 and (E)-6. The [4 + 2]-cycloaddition of 5 and PhC≡CPh in yielding the barrelene-type bis-silylene [(ADC)SiCPh]2 (7) emphasizes the diradical reactivity of 5. With elemental sulfur, 5 results in the S2- and S3-bridged silathione derivatives [(ADC)Si(S)]2(μ-S2) (8a) and [(ADC)Si(S)]2(μ-S3) (8b). Moreover, the treatment of 5 with Fe2(CO)9 affords the Fe(0) complex [(ADC)Si(Fe(CO)4)]2(μ-CO) (9), in which each silicon atom serves as a two-electron σ-donor ligand and shares one electron with the bridging CO unit to form two Si-C bonds. The molecular structures of all compounds have been established by X-ray diffraction, and representative compounds have been analyzed by quantum chemical calculations.

Structural and electronic properties of amorphous silicon and germanium monolayers and nanotubes: A DFT investigation

A recent breakthrough has been achieved by synthesizing monolayer amorphous carbon (MAC). Here, we used ab initio (DFT) molecular dynamics simulations to study silicon and germanium MAC analogs. Typical unit cells contain more than 600 atoms. We also considered their corresponding nanotube structures. The cohesion energy values for MASi and MAGe are approximately 3.0 eV/atom lower than the energy ordering of silicene and germanene, respectively. Their electronic behavior varies from metallic to small band gap semiconductors. Since silicene, germanene, and MAC have already been experimentally realized, the corresponding MAC-like versions we propose are within our present synthetic capabilities.

Stabilization and One Electron Reduction of a Silicon Analogue of a Carboxylic Acid Anhydride.

Reaction of the 1,2-disilylenes {(DipAr Am)Si}2 (DipAr Am=[(NDip)2 CAr]- , Dip=2,6-diisopropylphenyl, Ar=4-C6 H4 But (Ar') 1 a or Ph 1 b) and two abnormal N-heterocyclic silylenes, (DipAr Am)SiOCSi{(NDip)2 CAr} (Ar=Ar' 3 a or Ph 3 b) with N2 O led to formation of unprecedented examples of uncoordinated silicon analogues of carboxylic acid anhydrides, (DipAr Am)(O=)SiOSi(=O)(DipAr Am) (Ar=Ar' 2 a or Ph 2 b). Both compounds have been fully characterized, and the mechanism of formation of one explored using DFT calculations. Reduction of sila-acid anhydride 2 a with a dimagnesium(I) compound, [{(Mes Nacnac)Mg}2 ] (Mes Nacnac=[(MesNCMe)2 CH]- , Mes=mesityl), led to the one-electron reduction of the anhydride and formation of a magnesium complex of a sila-acid anhydride radical anion [(Mes Nacnac)Mg{(OSi(DipAr' Am)}2 O] 5. A combination of EPR spectroscopic studies and DFT calculations reveal the unpaired electron to largely reside on one of the amidinate ligands of the complex.

Theoretical investigation of the vibrational and electronic properties of tetraphenylammonium and its boron, aluminum, gallium, carbon, silicon, germane, phosphorus and arsenic analogues

Tetraphenyl ammonium (Ph4N+ ) has long been considered a phantom ion due to the difficulty in synthesizing aryl ammonium compounds. Following the successful synthesis of Ph4N+ last year (2022), the equilibrium geometries of Ph4X (X = B-, Al-, and Ga- of group 13; C, Si, and Ge of group 14; and P+ and As+ of group 15) have been optimized using the B3LYP/6-31G(d,p) method with no symmetry constraints. According to the optimized structural data, Ph4N+ is considered the most sterically hindered molecule in this series of compounds, which reflects the difficulty of its synthesis. The calculated total energies of the Ph4X compounds reveal that their energies decrease down the group, and the cationic forms (group 15) are less energetic than their neutral (group 14) and anionic (group 13) counterparts. The optimized geometrical parameters were used to compute the UV–vis, IR, 1H NMR, and 13C NMR spectra of the nine terephenyl compounds. The frontier molecular orbital energies were used to determine ionization potentials, electron affinity, and other global reactivity descriptors of the nine Ph4X compounds. An accurate assignment of vibrational bands was made using the potential energy distribution (PED) method. The B3LYP/6-31G(d,p) method yielded good agreement with available experimental data for the molecules. The low HOMO-LUMO gaps suggest potential nonlinear optical properties of these compounds.

Silicon analogues of unsaturated hydrocarbons

The proposed communication demonstrates the efforts of researchers undertaken to prove the existence of fundamental analogies in the chemistry of structurally related compounds of carbon and silicon. Stable silicon analogues of ethylene - silenes or silaethylenes R2C=SiR2 - were obtained in 1979, disilynes R2Si=SiR2 - in 1981, and analogues of ethine or acetylene - disilins RSi≡SiR - only in 2004. Moving towards the intended goals, scientists synthesized a number of unique branched (bulky) organic and organosilicon substituents, attached them to silicon atoms, closed them from the action of oxygen and air moisture, and prevented secondary dimerization (oligomerization) reactions. The created steric protection led to the preparation of kinetically stable unsaturated silicon compounds and made it possible to characterize them by IR, NMR, UV-visible spectroscopy, and X-ray diffraction analysis.

Silicon Analogs of Unsaturated Hydrocarbons

Silicon Analogs of Unsaturated Hydrocarbons

Polysilyne chains bridged with beryllium lead to flat 2D Dirac materials

Polysilyne with repeating disilyne units, a silicon analogue of polyacetylene, has a high potential for application to various novel silicon-based electronic devices because of the unique properties of Si=Si units with a smaller HOMO–LUMO energy gap than that of C=C units. However, one-dimensional (1D) polysilyne has not been synthesized yet. Here we propose a planar and air-stable two-dimensional (2D) silicon-based material with one-atom thickness consisting of beryllium-bridged 1D all-trans polysilyne, based on the first-principles calculations. The flat structure of 1D polysilyne, which is essential for the air stability of silicon π-electron conjugated systems, is realized by embedding polysilyne in a planar sheet. It was found that the 2D crystal optimized at the rhombus unit cell with the D2h group symmetry is a silicon-based Dirac semimetal with linear dispersion at the Fermi energy and hosts anisotropic Dirac fermions.

Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: An effective strategy towards development of potent anti-tubercular agents

Growing global demand for new molecules to treat tuberculosis has created an urgent need to develop novel strategies to combat the menace. BM212 related compounds were found to be potent anti-TB agents and they inhibit mycolic acid transporter, MmpL3, a known potent drug target from Mycobacterium tuberculosis. In order to enhance their inhibitory potency, several silicon analogues of diarylpyrroles related to BM212 were designed, synthesized, and evaluated for anti-tubercular activities. In Alamar blue assay, most of the silicon-incorporated compounds were found to be more potent than the parent compound (BM212), against Mycobacterium tuberculosis (MIC = 1.7 μM, H37Rv). Docking results from the crystal structure of MmpL3 and silicon analogues as pharmacophore model also strongly correlate with the biological assays and suggest that the incorporation of silicon in the inhibitor scaffold could enhance their potency by stabilizing the hydrophobic residues at the binding pocket. The best docking hit, compound 12 showed an MIC of 0.1 μM against H37Rv with an acceptable in vitro ADME profile and excellent selectivity index. Overall, the present study indicates that, the designed silicon analogues, especially compound 12 could be a good inhibitor for an intrinsically flexible drug-binding pocket of MmpL3 and has potential for further development as anti-tubercular agents.

Robert C. West (1928–2022): A Giant in Organosilicon Chemistry, Cosmopolitan, Mountain Climber and Pilot

Robert C. West (1928–2022): A Giant in Organosilicon Chemistry, Cosmopolitan, Mountain Climber and Pilot

Cyclobutenylidene: A Multifaceted Two-Coordinate Carbon Species Obtained via Skeletal Editing of a Cyclopropenylidene

C4H4 isomers not only serve as a basis to understand the chemical properties of hydrocarbons but are possible intermediates in combustion and organic reactions in outer space. Cyclobutenylidene (CBY), an elusive C4H4 isomer, is often proposed as a key intermediate in transition-metal-catalyzed metathesis and cycloaddition reactions between carbon-carbon multiple bonds. The geometrical structure of cyclobutenylidene predicted by calculations had been debated as whether it should be regarded as a carbocyclic carbene or a strained bridgehead alkene. Here, we report the synthesis of a crystalline cyclobutenylidene derivative, namely, a 3-silacyclobut-2-en-4-ylidene (SiCBY) via "carbene-to-carbene ring-expansion" reaction of an isolable diaminocyclopropenylidene induced by a silicon analogue of a carbene (silylene). The SiCBY exhibits multifaceted electronic properties which are corroborated by its extremely strong electron-donating properties and ambiphilic reactivity toward small gaseous molecules and C-H bonds. This result introduces an exciting strategy as well as a molecular motif to access low-valent carbon species with unusual electronic properties.

Theoretical Study of Si/C Equally Mixed Dodecahedrane Analogues

To gain insight into the effect of Si/C arrangement on the molecular framework of strained polyhedral compounds, dodecahedrane analogues containing equal numbers of carbon and silicon (Si/C equally mixed dodecahedrane analogues) were investigated using the ab initio molecular orbital method. There are 1648 isomers for which the Si/C arrangement on the molecular framework is different. Based on the geometry optimization of all the isomers as well as the carbon and silicon analogues, the characteristics of the structure, relative energy, and strain energy of the Si/C equally mixed compounds are presented. Then, important factors controlling the relative energy, such as strain energy, are proposed through regression analysis. Also discussed is the correlation between the relative energy and the indices of Si/C dispersion, such as the number of skeletal C-Si single bonds and condensed five-membered rings constituting the polyhedral structure.

Theoretical descriptions of novel silicon analogs of cyclo[18]carbon

AbstractThe effects of substituting silicon atoms on the stability, geometrical parameters, and electronic properties of cyclo[18]carbon (C18), C17Si, and nine isomers of C16Si2 (C16Si2(0) to C16Si2(8)) are compared and contrasted at CAM‐B3LYP/6‐311G* level of theory. Among C16Si2 isomers, the trend of stability (based on total and binding energy [Eb]) is C16Si2(8) > C16Si2(4) > C16Si2(2) > C16Si2(7) > C16Si2(6) > C16Si2(5) > C16Si2(3) > C16Si2(1) > C16Si2(0), at B3LYP/6‐311G*, B3LYP/6‐311++G**, WB97XD/6‐311G*, and CAM‐B3LYP/6‐311G* level of theories. Respectively, the highest and lowest band gaps belong to C18 and C17Si, which also have the smallest and largest conductivities. According to the heat of atomization per carbon (ΔHat/C) and heat of formation (ΔHf), the least thermodynamic stable species, C16Si2(0), suffers from the highest inter‐atomic interaction of neighboring silicon atoms (Si‐Si repulsion) and the most thermodynamic stable species, C16Si2(8), that has the furthest silicon atoms from each other. Theoretical analysis indicates that the most chemically reactive isomers are C16Si2(1), (3), and (5), which have high nucleophilicity (N = 2.752, 2.665, and 2.573 eV, respectively) and electrophilicity (ω = 0.126, 0.128, and 0.128 eV, respectively). The Si substitution increases the polarizability and activity of rings to interact with their surrounding polar species.

Solar cells based on CdTe thin films (Part II)

This paper discusses the use of semiconductor solar cells based on thin-film cadmium telluride (CdTe) in modern energy production. The advantages and disadvantages of using CdTe thin-film solar cells are analyzed, and arguments are presented in favor of the implementation of mass production technologies for CdTe solar modules, which can compete with silicon analogs in terms of compromise between efficiency and cost. The physical and chemical properties of the binary Cd-Te system are described, and the relationship between the physical, chemical, electrical, and optical properties of CdTe is analyzed, making it attractive for use in thin-film solar cells. Special attention is given to the investigation of photovoltaic properties, which are important parameters for determining photoconductivity, and the advantages and disadvantages of CdTe film photovoltaic properties are discussed. CdTe thin-film heterostructures (HSs), which are important components of modern solar cells, are considered, and their main advantages and disadvantages are described. It is argued that simple methods of manufacturing and forming HSs, which do not require complex and expensive equipment, are an important advantage of CdTe-based solar cell technology.

Structural and thermal properties of Eu2Ga11Sn35

Clathrates have been reported to form in a variety of different structure types; however, inorganic clathrate-I materials with a low-cation concentration have yet to be investigated. Furthermore, tin-based compositions have been much less investigated as compared to silicon or germanium analogs. We report the temperature-dependent structural and thermal properties of single-crystal Eu2Ga11Sn35 revealing the effect of structure and composition on the thermal properties of this low-cation clathrate-I material. Specifically, low-temperature heat capacity, thermal conductivity, and synchrotron single-crystal x-ray diffraction reveal a departure from Debye-like behavior, a glass-like phonon mean-free path for this crystalline material, and a relatively large Grüneisen parameter due to the dominance of low-frequency Einstein modes. Our analyses indicate thermal properties that are a direct result of the structure and composition of this clathrate-I material.

Room Temperature Intermolecular Dearomatization of Arenes by an Acyclic Iminosilylene.

A novel nontransient acyclic iminosilylene (1), bearing a bulky super silyl group (-SitBu3) and N-heterocyclic imine ligand with a methylated backbone, was prepared and isolated. The methylated backbone is the feature of 1 that distinguishes it from the previously reported nonisolable iminosilylenes, as it prevents the intramolecular silylene center insertion into an aromatic C-C bond of an aryl substituent. Instead, 1 exhibits an intermolecular Büchner-ring-expansion-type reactivity; the silylene is capable of dearomatization of benzene and its derivatives, giving the corresponding silicon analogs of cycloheptatrienes, i.e. silepins, featuring seven-membered SiC6 rings with nearly planar geometry. The ring expansion reactions of 1 with benzene and 1,4-bis(trifluoromethyl)benzene are reversible. Similar reactions of 1 with N-heteroarenes (pyridine and DMAP) proceed more rapidly and irreversibly forming the corresponding azasilepins, also with nearly planar seven-membered SiNC5 rings. DFT calculations reveal an ambiphilic nature of 1 that allows the intermolecular aromatic C-C bond insertion to occur. Additional computational studies, which elucidate the inherent reactivity of 1, the role of the substituent effect, and reaction mechanisms behind the ring expansion transformations, are presented.

Silicon-Containing Complex II Acaricides─Design, Synthesis, and Pharmacological Optimization.

Bioisosteric replacement has been proven to be a powerful strategy in life science research. In this review, general aspects of carbon-silicon bioisosteric substitution and its applications in pharmaceutical and crop protection research are described. Carbon and their silicon analogues possess similar intrinsic properties. Replacing carbon with silicon in pharmaceuticals and pesticides has shown to result in positive effects on efficacy and selectivity, physicochemical properties, and bioavailability and also to eliminate or improve human or environmental safety properties as well as to provide novelty and new intellectual property in many cases. Furthermore, the application of carbon-silicon substitution in the search for new complex II acaricides is highlighted. This research led to the discovery of sila-cyflumetofen 23a and other silicon-containing analogues of cyflumetofen that match or exceed the acaricidal activity of cyflumetofen. The molecular design strategy, synthetic aspects, biological activity, computational modeling work, and structure-activity relationships will be discussed.

Silicon Analogs of L-Amino Acids: Properties of Building Blocks of an Alien Biosphere

Silicon Analogs of L-Amino Acids: Properties of Building Blocks of an Alien Biosphere

Synthesis, Structure and Electronic Properties of a Stable π‐Type 3‐Electron‐2‐Center‐Bonded Species: A Silicon Analogue of a Bicyclo[1.1.0]butane Radical Anion

σ-Type 3-electron-2-center (3e-2c) bonds have been extensively studied as one of the key bonding motifs in radical chemistry and some biological systems. “π-Type 3e-2c-bonded species” that contain a 3e-2c π-bond without an underlying σ-bond framework, however, have been unexplored so far both theoretically and experimentally. Herein, we report the synthesis of the first stable π-type 3e-2c-bonded species, a silicon analogue of a bicyclo[1.1.0]butane radical anion. This compound exhibits an extremely long bridgehead Si−Si bond (3.0638(8) Å) and a strong near-IR absorption at 922 nm in solution which arises from a HOMO→SOMO [π(Si−Si)→π*(Si−Si)] transition. DFT calculations revealed a π-type bonding interaction between the two bridgehead silicon atoms with an unpaired electron mainly delocalized across the corresponding π*-type orbital, which introduces a novel bonding motif for constructing π-electron systems.

Synthesis, Structure and Electronic Properties of a Stable π-Type 3-Electron-2-Center-Bonded Species: A Silicon Analogue of a Bicyclo[1.1.0]butane Radical Anion.

σ-Type 3-electron-2-center (3e-2c) bonds have been extensively studied as one of the key bonding motifs in radical chemistry and some biological systems. "π-Type 3e-2c-bonded species" that contain a 3e-2c π-bond without an underlying σ-bond framework, however, have been unexplored so far both theoretically and experimentally. Herein, we report the synthesis of the first stable π-type 3e-2c-bonded species, a silicon analogue of a bicyclo[1.1.0]butane radical anion. This compound exhibits an extremely long bridgehead Si-Si bond (3.0638(8) Å) and a strong near-IR absorption at 922 nm in solution which arises from a HOMO→SOMO [π(Si-Si)→π*(Si-Si)] transition. DFT calculations revealed a π-type bonding interaction between the two bridgehead silicon atoms with an unpaired electron mainly delocalized across the corresponding π*-type orbital, which introduces a novel bonding motif for constructing π-electron systems.

Activation of CO Using a 1,2-Disilylene: Facile Synthesis of an Abnormal N-Heterocyclic Silylene.

Reaction of the 1,2-disilylene, [{ArC(NDip)2 }Si]2 1 (Dip=2,6-diisopropylphenyl, Ar=4-C6 H4 But ), with CO proceeds via insertion of CO into one Si-N bond, and Si-Si bond cleavage, to cleanly give the bis(silylene), {ArC(NDip)2 }Si(:)O Ar 2, under ambient conditions. The reaction can be partially reversed when solutions of 2 are subjected to UV irradiation. The five-membered heterocyclic fragment of 2 represents the first silicon analogue of an "abnormal" N-heterocyclic carbene (aNHC), a view which is substantiated by a computational analysis of the compound. Reaction of 2 with [Mo(CO)6 ] under UV light affords the chelate complex, [Mo(CO)4 (κ2 -Si,Si-2)] 3, while reaction with [Fe(CO)5 ] gives the unusual silyleneyl bridged complex, [{Fe2 (CO)6 }{μ-Si[(NDip)2 CAr]}2 ] 4. The same coordination complexes can be accessed by reaction of 1 with [Mo(CO)6 ] or [Fe(CO)5 ] under UV light. As is the case for aNHCs, d-block metal complexes of bis(silylene) 2 could prove useful as bespoke catalysts for organic transformations.