Beryllium carbonyl Be(CO)n (n = 1-4) complex: a p-orbital analogy of Dewar-Chatt-Duncanson model.

Transition metal-carbonyl bonds are rationalized by M ← CO σ donation and M → CO π back donation where the d orbital of the transition metal is involved. This bonding model provided by Dewar, Chatt and Duncanson (DCD) has rationalized many transition metal-ligand bonds. The involvement of p orbital in such a DCD model can be intriguing. Alkaline earth metals with ns2np0 configuration may appear suitable as ns0np2 excitation has been recognized in many complexes. Herein, a theoretical study is presented for the Be(CO)n (n = 1-4) complex to verify this assumption. Detailed electronic structure analyses confirmed the involvement of the p orbital of beryllium in M → CO π back donation, thereby supporting the hypothesis. EDA-NOCV results reveal that the π-back donation from the central Be atom to CO ligands significantly predominates over the σ donation from the ligands for both Be(CO)3 and Be(CO)4. Our calculations reveal that Be(CO)4 is the highest carbonyl that may be experimentally detected.

Pushing The Extreme of Multicentre Bonding: Planar Pentacoordinate Hydride.

Planar hypercoordination has sparkled interest among the researchers from last few decades. Most of the elements in the Periodic Table have shown this remarkable structural feature. However, the smallest element, hydrogen, is missing in the list. No evidence is there in the literature. Herein, we introduce the first planar pentacoordinate hydrogen atom (ppH) in the global minimum geometry of Li5 H6 - cluster. Bonding analysis indicates that the central hydrogen atom is stabilized by multicentre bonding with five surrounding Li atoms. Natural charge analysis reveals that the central hydrogen is acting like a hydride which is strongly attracted by the positively charged surrounding lithium centres. The ppH structure is stabilized by strong electrostatic attraction as well as extensive multicentre bonding. Aromaticity has no role to play here. The cluster is dynamically stable and is expected to be detected in gas phase.

Enhancing Precatalyst Performance and Robustness through Aromaticity: Insights from Iridaheteroaromatics.

Despite the inherent stability-enhancing benefits of dπ-pπ conjugation-induced aromaticity, metallaaromatic catalysts remain underutilized in this context, despite their reactivity with organic functionalities in stoichiometric reactions. We present a strategy for synthesizing a diverse range of iridaheteroaromatics, (L^L)IrIII(Cp*)I, including iridapyridylidene-indole, iridapyridene-indole, and iridaimidazole, via in situ deprotonation/metalation reactions utilizing [Cp*IrCl2]2 and the respective ligands. These catalysts exhibit enhanced σ-donor and π-acceptor properties, intrinsic σ-π continuum attributes, and versatile binding sites, contributing to stability through enhanced dπ-pπ conjugation-induced aromaticity. Spectroscopic data, X-ray crystallographic data, and density functional theory calculations confirm their aromaticity. These iridaheteroaromatics exhibit formidable catalytic ability across a spectrum of transformations under industrially viable conditions, notably excelling in highly selective cross alkylation and ß-alkylation of alcohols and an eco-friendly avenue for quinolone synthesis, achieving remarkably high turnover frequencies (TOFs). Additionally, this method extends to the self-condensation of bioalcohols like ethanol, n-butanol, and n-hexanol in water, replicating conditions frequently encountered in primary fermentation solutions. These iridaheteroaromatics exhibit strong catalytic activity with fast reaction rates, high TOFs, broad substrate compatibility, and remarkable selectivity, displaying their potential as robust catalysts in large-scale applications and emphasizing their practical significance beyond their structural and theoretical importance.

Highly Luminescent Eu3+-Incorporated Zr-MOFs as Fluorescence Sensors for Detection of Hazardous Organic Compounds in Water and Fruit Samples.

Considering the risk of toxic organic compounds to both human health and the environment, highly luminescent Eu3+-incorporated amino-functionalized zirconium metal-organic frameworks, namely, Eu/MOF and Eu@MOF were synthesized via the solvothermal method. The synthesized luminescent europium-incorporated MOFs act as outstanding sensor materials for diphenylamine and dinitrobenzene detection in water and fruit samples. The synergistic effect of Eu3+ metal ions and amino-functionalized MOFs enhances the luminescent properties of the MOFs improving the fluorescence sensing ability toward the analytes. The enhancement in the detection capacity of the Eu3+-incorporated sensors than the sole MOF toward toxic organic compounds was confirmed using the Stern-Volmer equation of limit of detection (LOD) measurements along with fluorescence lifetime measurements. The sensors exhibited turn-on fluorometric detection toward their respective analytes due to the inner filter effect. The plausible fluorescence sensing mechanism has been studied. The DFT calculations have been integrated to study the structure, stability, and charge transfer processes.

Sequential organo and metal catalyzed reaction between 3-pyrrolyloxindoles and linear nitroenynes: access to cyclic aza-spirooxindoles.

An asymmetric Michael addition/hydroarylation reaction sequence, catalyzed by a sequential catalytic system consisting of a squaramide and a combination of silver and gold salts, provides a new series of cyclic aza-spirooxindole derivatives in excellent yields (up to 94%) and high diastero- and enantioselectivities (up to 7 : 1 dr, up to >99% ee). Computational study has also been performed.

Palladium-Catalyzed Annulative Coupling of Spirovinylcyclopropyl Oxindoles with p-Quinone Methides.

Pd-catalyzed annulative coupling of spirovinylcyclopropyl oxindoles with p-quinone methides has been accomplished via cascade carbon-carbon bond formation to afford bis-spirooxindole scaffolds. The mild reaction conditions, diastereoselectivity, functional group diversity, post-synthetic transformations, and mechanistic studies using DFT calculations are the important practical features.

Cobalt-Catalyzed Stereospecific C-N/C-O Bond Formation of Oxiranes with Diaziridines.

Co-catalyzed stereospecific C-N and C-O bond formation of oxiranes with diaziridines has been accomplished to furnish tetrahydro-[1,3,4]-oxadiazines at room temperature. Optically active oxiranes can be coupled with high optical purities (>96% ee). Stereoselectivity, functional group tolerance, mechanistic studies using DFT, and natural product modification are the important practical features.

Heterogeneous iron catalyst for C(1)-H functionalization of 2-naphthols with primary aromatic alcohols.

An iron oxide nanocatalyst supported on a potassium exchanged zeolite-Y (Fe2O3-KY) is an efficient and reusable catalyst that promotes the selective α-H functionalization of 2-naphthols with various aromatic primary alcohols. The reaction occurs at 110 °C in dichloroethane and requires 6 h for completion. The product yields were found to vary with respect to the nature of the substituents. Benzyl alcohols with electron-donating groups gave the highest yields of up to 90%.

An in silico study of the selective adsorption and separation of CO2 from a flue gas mixture (CH4, CO2, N2) by ZnLi5+ clusters.

Due to the increasing concentration of CO2 in the atmosphere and its negative effect on the environment, selective adsorption of CO2 from flue gas has become significantly important. In this study, we have considered a Zn-doped lithium cluster, ZnLi5+ cluster, featuring a planar pentacoordinate Zn centre, as a potential candidate for selective CO2 capture and separation from a flue gas mixture (CH4, CO2, N2). The binding energy calculation and non-covalent interaction study showed that CO2 molecules bind relatively strongly as compared to N2 and CH4 molecules. The metal cluster can bind five CO2, five CH4, and four N2 molecules with average binding energies of -9.2, -4.4, and -6.1 kcal mol-1, respectively. Decomposition of the binding energy through symmetry-adapted perturbation theory analysis reveals that the electrostatic component plays a major role. The cationic cluster may be a promising candidate for selective CO2 capture and can be used as a pollution-controlling agent. The calculated adsorption energy of H2S is quite closer to that of CO2, suggesting competitive adsorption between CO2 and H2S. The adsorption energies of H2O and NH3 are higher compared to CO2, indicating that these gases may be a potential threat to CO2 capture.

Inorganic Bergman Cyclization: An Appeal From Theory.

The scope of Bergman cyclization is expanded computationally by exploring the cyclization in inorganic B, N substituted derivative. This substitution has introduced polarity into the transition state, which resulted in dramatic lowering of the activation barrier. Natural charge distribution throughout the reaction profile has ascertained this hypothesis. Single B and N atom substitution at 1 and 6 terminal positions lowers the activation barrier by almost half of the original value which becomes even lower in the complete B, N analogue. The parent Bergman and single B, N substituted products were characterized by significant biradical character while the complete B, N substituted analogue was characterized by significant zwitterionic character. Reduction in electron delocalization is also observed in the complete B, N substituted analogue.

Ultra-high reversible hydrogen storage capacity of the Li4B2 cluster: a quantum chemical study.

Quantum chemical calculations have been carried out to investigate the hydrogen adsorption characteristics of the Li4B2 cluster. Calculations reveal that the cluster can adsorb a maximum of thirteen H2 molecules reaching a considerably high gravimetric density of 34.66 wt%. The nature of the interaction between the H2 molecule and Li center has been investigated within the realm of quantum theory of atoms in molecules which revealed the non-covalent character. The fate of H2 absorption by the cluster has been studied in the course of a 2000 fs time evolution through Born-Oppenheimer molecular dynamics simulations at different temperatures. The outcomes reveal that the H2 molecules are strongly bound at 77 K and get slowly released at elevated temperatures.

Can an alkalide act as a perfect Lewis base?

The Lewis basic character of alkali metals forming donor-acceptor complexes is a very rare phenomenon. No Lewis adduct with an alkalide as the Lewis basic centre has ever been reported. Herein, we theoretically designed EXH2- (E = Li, Na, K; X = Be, Mg, Ca) clusters which represent the first true example of Lewis adducts with alkalides as the two-electron donor basic sites. Our high level ab initio calculations reveal the formation of an unprecedented E:- → XH2 donor-acceptor interaction. Topological analysis within the realm of the electron localization function confirms this bonding scenario. The bonding scenario is exactly replicated in all the clusters, rendering support to our proposal. The calculated bond dissociation energies are significant, suggesting their possible spectroscopic identification.