Symmetry-forbidden Research Articles

Origin of a Kinetically Selective Route for Thermoreversible Valence Tautomerism-Based Photoswitching in O-Heterocycles Containing Conjugated Dienes.

The thermal electrocyclic ring opening of fused cis-cyclobutene to cis,cis-diene is prohibited according to the Woodward-Hoffmann (WH) rules; nonetheless, experiments provide firm evidence for their formation. However, the mechanism, electronic structure, and behavior during the reaction are ambiguous. Herein, we attempt to gain insights into the mechanism of thermal ring opening in four O-heterocycles containing a conjugated diene as the core skeleton. The results emphasize that the reaction initiates with a conrotatory ring opening to produce a cis,trans-diene as a strained transient intermediate following the WH rules but ultimately leads to a forbidden product. The conversion of cis,trans-diene to cis,cis-diene is kinetically preferred through double-bond rotation, involving the formation of a singlet biradicaloid. The expected H-shift is unfavorable because the requirement of suprafacial H transfer incorporates additional strain, while the transfer of other available H is symmetry-forbidden. The increased electrophilicity at O promotes C-O dissociation in the 8-membered cyclic cis,trans-dienes with fused benzene. This enables thermoreversible photoswitching via a two-step mechanism and kinetically refutes the direct disrotatory pathway. These systems can outperform energy storage, and critical insight into their mechanism with the aid of comprehensive electronic structure analysis would assist in their rational design in the future.

Internal Electric Fields and Structural Instabilities in Insulating Transition Metal Compounds: Influence on Optical Properties

AbstractThis work reviews new ideas developed in the last two decades which play a key role for understanding the optical properties of insulating materials containing transition metal (TM) cations. Initially, this review deals with compounds involving d4 and d9 ions where the local structure of the involved MX6 complexes (M=dn cation, X=ligand) is never cubic but distorted, a fact widely ascribed to the Jahn‐Teller (JT) effect. Nevertheless, that assumption is often wrong as the JT coupling requires an orbitally degenerate ground state in the initial geometry a condition not fulfilled even if the lattice is tetragonal. For this reason, the equilibrium geometry of d4 and d9 complexes in low symmetry lattices, is influenced by two factors: (i) The effects, usually ignored, of the internal electric field, ER, due to the rest of lattice ions on the active electrons localized in the MX6 unit. (ii) The existence of structural instabilities driven by vibronic interactions that lead to negative force constants. As first examples of these ideas, we show that the equilibrium structure, electronic ground state of KZnF3:Cu2+, K2ZnF4:Cu2+ and K2CuF4 obey to different causes and only in KZnF3:Cu2+ the JT effect takes place. These ideas also explain the local structure and optical properties of CuF2, CrF2 or KAlCuF6 compounds where the JT effect is symmetry forbidden and those of layered copper chloroperovskites where the orthorhombic instability explains the red shift of one d−d transition under pressure. In a second step, this review explores stable systems involving d3, d5 or d9 cations, where the internal electric field, ER, is responsible for some puzzling phenomena. This is the case of ruby and emerald that surprisingly exhibit a different color despite the Cr3+‐O2− distance is the same. A similar situation holds when comparing the normal (KMgF3) and the inverted (LiBaF3) perovskites doped with Mn2+ having the same Mn2+‐F distance but clearly different optical spectra. The role of ER is particularly remarkable looking for the origin of the color in the historical Egyptian Blue pigment based on CaCuSi4O10.

Impact of the Peripheral Ligand Layer on the Excited-State Deactivation Mechanism of Au38S2(S-Adm)20 and Au30(S-Adm)18 (S-Adm = Adamantanethiolate) Clusters.

Gold nanoclusters are ideal fluorescent labels for biological imaging, disease diagnosis, and treatment. Understanding the origin of the photoluminescence phenomenon in ligand-protected gold nanoclusters is crucial for both basic science and practical applications. In this study, density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations were performed to study the mechanism of excited state deactivation of Au38S2(S-Adm)20 and Au30(S-Adm)18 (S-Adm = adamantanethiolate) clusters, which have similar sizes and compositions. The computational results indicate that the differences in structural symmetry and peripheral ligand layer lead to quite different excited state deactivation mechanisms and excited state lifetimes in Au38S2(S-Adm)20 and Au30(S-Adm)18. Specifically, the μ3-S atoms and bridging thiolate (SR) in the ligand layer of Au38S2(S-Adm)20 significantly suppress the structural relaxation of ligand motifs, resulting in a prolonged excited state lifetime and higher quantum yield. For the Au30(S-Adm)18, due to the symmetry forbidden and large structural relaxation of the ligand shell, a rapid nonradiative transition process resulted. This study provides new insights into how the photoluminescence of ligand-protected gold nanoclusters is influenced by their structure and symmetry.

Predictive Guidelines for Electrocyclization of Dithienylethenes.

Molecular photoswitches undergo a structural transformation upon photoexcitation to interconvert between two or more stable forms. In some cases, the structural rearrangement involves the transition between ring-open and ring-closed forms. In this work, we develop simple guidelines for the design of organic molecules able to undergo photochemical electrocyclization, using electronic structure calculations on dithienylethene (DTE)-based compounds. We conclude that the ability to photocyclize can be predicted from the localization and symmetry of frontier molecular orbitals. These ideas are based on the Woodward-Hoffmann rules but go beyond them, allowing us to address a more general family of chromophores. Our methodology has been experimentally validated in a novel series of quinoline-based DTEs, where the ability for photocyclization depends on specific chemical modifications. We use the DTE scaffold as the workhorse model in our study; however, these simple yet powerful guidelines are expected to be generally valid to guide the design of other diarylethenes.

Hunting for the Intermolecular Diels-Alderase.

ConspectusThe Diels-Alder reaction is well known as a concerted [4 + 2] cycloaddition governed by the Woodward-Hoffmann rules. Since Prof. Otto Diels and his student Kurt Alder initially reported the intermolecular [4 + 2] cycloaddition between cyclopentadiene and quinone in 1928, it has been recognized as one of the most powerful chemical transformations to build C-C bonds and construct cyclic structures. This named reaction has been widely used in synthesizing natural products and drug molecules. Driven by the synthetic importance of the Diels-Alder reaction, identifying the enzyme that stereoselectively catalyzes the Diels-Alder reaction has become an intriguing research area in natural product biosynthesis and biocatalysis. With significant progress in sequencing and bioinformatics, dozens of Diels-Alderases have been characterized in microbial natural product biosynthesis. However, few are evolutionally dedicated to catalyzing an intermolecular Diels-Alder reaction with a concerted mechanism.This Account summarizes our endeavors to hunt for the naturally occurring intermolecular Diels-Alderase from plants. Our research journey started from the biomimetic syntheses of D-A-type terpenoids and flavonoids, showing that plants use both nonenzymatic and enzymatic intermolecular [4 + 2] cycloadditions to create complex molecules. Inspired by the biomimetic syntheses, we identify an intermolecular Diels-Alderase hidden in the biosynthetic pathway of mulberry Diels-Alder-type cycloadducts using a biosynthetic intermediate probe-based target identification strategy. This enzyme, MaDA, is an endo-selective Diels-Alderase and is then functionally characterized as a standalone intermolecular Diels-Alderase with a concerted but asynchronous mechanism. We also discover the exo-selective intermolecular Diels-Alderases in Morus plants. Both the endo- and exo-selective Diels-Alderases feature a broad substrate scope, but their mechanisms for controlling the endo/exo pathway are different. These unique intermolecular Diels-Alderases phylogenetically form a subgroup of FAD-dependent enzymes that can be found only in moraceous plants, explaining why this type of [4 + 2] cycloadduct is unique to moraceous plants. Further studies of the evolutionary mechanism reveal that an FAD-dependent oxidocyclase could acquire the Diels-Alderase activity via four critical amino acid mutations and then gradually lose its original oxidative activity to become a standalone Diels-Alderase during the natural evolution. Based on these insights, we designed new Diels-Alderases and achieved the diversity-oriented chemoenzymatic synthesis of D-A products using either naturally occurring or engineered Diels-Alderases.Overall, this Account describes our decade-long efforts to discover the intermolecular Diels-Alderases in Morus plants, particularly highlighting the importance of biomimetic synthesis and chemical proteomics in discovering new intermolecular Diels-Alderases from plants. Meanwhile, this Account also covers the evolutionary and catalytic mechanism study of intermolecular Diels-Alderases that may provide new insights into how to discover and design new Diels-Alderases as powerful biocatalysts for organic synthesis.

Unraveling the Rich Fragmentation Dynamics Associated with S-H Bond Fission Following Photoexcitation of H2S at Wavelengths ∼129.1 nm.

H2S is being detected in the atmospheres of ever more interstellar bodies, and photolysis is an important mechanism by which it is processed. Here, we report H Rydberg atom time-of-flight measurements following the excitation of H2S molecules to selected rotational (JKaKc') levels of the 1B1 Rydberg state associated with the strong absorption feature at wavelengths of λ ∼ 129.1 nm. Analysis of the total kinetic energy release spectra derived from these data reveals that all levels predissociate to yield H atoms in conjunction with both SH(A) and SH(X) partners and that the primary SH(A)/SH(X) product branching ratio increases steeply with ⟨Jb2⟩, the square of the rotational angular momentum about the b-inertial axis in the excited state. These products arise via competing homogeneous (vibronic) and heterogeneous (Coriolis-induced) predissociation pathways that involve coupling to dissociative potential energy surfaces (PES(s)) of, respectively, 1A″ and 1A' symmetries. The present data also show H + SH(A) product formation when exciting the JKaKc' = 000 and 111 levels, for which ⟨Jb2⟩ = 0 and Coriolis coupling to the 1A' PES(s) is symmetry forbidden, implying the operation of another, hitherto unrecognized, route to forming H + SH(A) products following excitation of H2S at energies above ∼9 eV. These data can be expected to stimulate future ab initio molecular dynamic studies that test, refine, and define the currently inferred predissociation pathways available to photoexcited H2S molecules.

An organic proton cage that is ultra-resistant to hydroxide-promoted degradation

Alkaline polymer membrane electrochemical energy conversion devices offer the prospect of using non-platinum group catalysts. However, their cationic functionalities are currently not sufficiently stable for vapor-phase applications, such as fuel cells. Herein, we report 1,6-diazabicyclo[4.4.4]tetradecan-1,6-ium (in-DBD), a cationic proton cage, that is orders of magnitude more resistant to hydroxide-promoted degradation than state-of-the-art organic cations under ultra-dry conditions and elevated temperature, and the first organic cation-hydroxide to persist at critically low hydration levels ( < 10% RH at 80 °C). This high stability against hydroxide-promoted degradation is due to the unique combination of endohedral protection and intra-bridgehead hydrogen bonding that prevents the removal of the inter-cavity proton and lowers the susceptibility to Hofmann elimination. We anticipate this discovery will facilitate a step-change in the advancement of materials and electrochemical devices utilizing anion-exchange membranes based on in-DBD that will enable stable operation under extreme alkaline conditions.

Tuning the Oxygen Reduction Reactivity of Layered Perovskites Using the Jahn-Teller Effect.

Compositional tuning of layered perovskite oxides provides a means of systematically studying how local distortions affect fundamental aspects of electrochemical reaction pathways. Structural analysis of a family of samples La1.2Sr0.8Ni1-yCoyO4 shows that Ni-rich compositions have an expanded crystalline c axis, which is anisotropically compressed by systematic Co incorporation. Raman spectra reveal the strong growth of a symmetry forbidden mode, which suggests that Co acts through localized distortions. Crystallographic and spectroscopic parameters describing this structural distortion correlate to the measured Tafel slopes for the oxygen reduction reaction for all Ni-containing samples, which is attributed to the distortion of potential energy surfaces by the Jahn-Teller expansion of d7 Ni(III) cations. Incorporation of Co not only minimizes the distortion but alters the apparent selectivity of the oxygen reduction reaction away from H2O2 and toward H2O. Rotating ring-disk electrochemical measurements, however, indicate that the apparent change in selectivity is due to activation of a first-order chemical disproportionation of H2O2 that is activated by Co in the lattice. These outcomes will support efforts to design electrocatalysts and reactors for the electrochemical synthesis of H2O2.

Strategies to Cope with Inferior Long-Term Photostability of Bentonite Polyolefin Nanocomposites.

This study provides insight into the causes of inferior long-term stability of nanocomposites based on organic layered silicates (OLSs) used for cable mantles. A hierarchy was established by analyzing bentonite products and their respective polyolefin nanocomposites. Thermogravimetric analysis (TGA), X-ray diffraction (XRD), gas adsorption, energy-dispersive spectroscopy (SEM-EDX), and infrared spectroscopy (IR) provided evidence for the adsorption of stabilizers onto the filler surface and thus their reduction in activity, promoting polymer oxidation. This behavior corresponds to the specific surface area of the incorporated OLS. Therefore, it can be stated that gas adsorption and XRD are especially useful for the evaluation of long-term photostability. It was revealed that photocatalytically active iron is of secondary importance since iron-rich bentonites still formed the most stable nanocomposite. This also applies to the Hofmann elimination products of the modifying agent, where higher contents do not accelerate the degradation process. No elimination products could be traced within the composites. Due to the polymer-filler interface being essential for long-term photostability, prior analysis of the filler surface properties can be used to estimate the stability of the respective nanocomposite as a rationale for product selection in the early stages of development. The reasons identified in this work for decreasing the long-term photostability of OLS nanocomposites compared with unfilled formulations is an important step toward increasing their stability.

Total absorption spectrum of benzene aggregates obtained from two different approaches.

The study of molecular aggregation effects on the electronic spectrum is essential for the development of optoelectronic devices. However, investigating the entire valence absorption spectrum of aggregates using quantum mechanical methods is a challenging task. In this work, we perform systematic simulations of the absorption spectrum of benzene molecular clusters up to 35 eV applying two approaches based on time-dependent density functional theory. The results show that depending on the dimer packing, different energy shifts occur for the symmetry allowed [Formula: see text] transition, in comparison to the monomer. The transition intensity increases for the band around 6 eV for larger aggregates from the monomer to dimers and tetramer, indicating the occurrence of the symmetry forbidden (in [Formula: see text] point group) [Formula: see text] [Formula: see text] transition. The benzene crystal exhibits a large redshift following the experimental spectrum. Also, the continuum regions of all spectra show a good agreement with the experiments both in gas and solid phases. Geometry optimization of the monomer was carried out with Gaussian 09 software using the PBE0/def2-TZVP level of theory. We used dimers and tetramer molecular geometries extracted from the experimental crystal structure. The absorption spectra were directly obtained by the Liouville-Lanczos TDDFT approach with plane waves basis set or indirectly by TDDFT pseudo-spectra calculated in a [Formula: see text] basis followed by analytic continuation procedure to obtain complex polarizability. The former is available at Quantum ESPRESSO, and the latter was calculated using Gaussian 09 with the post-processing performed with a code previously developed in our group.

Rh(III)‐Catalyzed sequential ring‐retentive/‐opening [4 + 2] annulations of 2H‐imidazoles towards full‐color emissive imidazo[5,1‐a]isoquinolinium salts and AIE‐active non‐symmetric 1,1′‐biisoquinolines

Rhodium-catalyzed C4aryl−H activation and ring-retentive annulation of 2H-imidazoles with internal alkynes to build imidazo[5,1-a]isoquinolinium salts with high yields and broad scope has been disclosed. These novel salts serve as new full-color emissive fluorophores (433−633 nm), just by simply modifying the substituents on C3 and C4 positions of isoquinoline ring. Furthermore, these salts can undergo ring-opening C5aryl−H activation/annulation with a different alkyne to form non-symmetric and AIE-active 1,1′-biisoquinolines, where NH4OAc plays an indispensable role that accounts for Hofmann elimination and imine formation, leading to an unprecedented imine dance: cyclic imine → N-alkenyl imine → NH imine. The 15N labelling experiments indicate that the 2nd annulation includes two pathways: N-exchange (major) and N-retention (minor).

Symmetry reduction induced by argon tagging gives access to low-lying excited states of FeH+ in the overtone region of the Fe-H stretching mode.

Iron is the most abundant transition metal in the interstellar medium (ISM), and is thought to be involved in a variety of astrochemical processes. Here, we present the infrared multiple photon dissociation (IRMPD) spectra of Ar1,2FeH+ and their deuterated isotopologues in the region of 2240-14 000 cm-1. The Fe-H overtone stretching mode in ArFeH+ and Ar2FeH+ is observed at 3636 ± 28 cm-1 and 3659 ± 13 cm-1, respectively. Deuteration shifts these bands to 2618 ± 31 cm-1 and 2650 ± 14 cm-1 in ArFeD+ and Ar2FeD+, respectively. Additionally, the spectra of Ar2FeH+ and Ar2FeD+ feature broad transitions at ∼2200-4000 cm-1 and ∼4500-6500 cm-1. We assign these bands to electronic transitions from the thermally populated X5A2/X'5A1 ground state manifold into the A'5B2 and B5A1 states, which we model with multi-reference quantum chemical calculations including spin-orbit coupling. The calculations show that these transitions are symmetry forbidden in FeH+ and in the equilibrium geometry of ArFeH+/ArFeD+, while the zero-point oscillation of the bending mode of the triatomic molecule leads to some oscillator strength. Upon addition of the second argon atom, the transitions become weakly allowed in the equilibrium geometry of Ar2FeH+/Ar2FeD+ due to symmetry reduction from C∞v to C2v.

A 21st Century View of Allowed and Forbidden Electrocyclic Reactions.

In 1965, Woodward and Hoffmann proposed a theory to predict the stereochemistry of electrocyclic reactions, which, after expansion and generalization, became known as the Woodward-Hoffmann Rules. Subsequently, Longuet-Higgins and Abrahamson used correlation diagrams to propose that the stereoselectivity of electrocyclizations could be explained by the correlation of reactant and product orbitals with the same symmetry. Immediately thereafter, Hoffmann and Woodward applied correlation diagrams to explain the mechanism of cycloadditions. We describe these discoveries and their evolution. We now report an investigation of various electrocyclic reactions using DFT and CASSCF. We track the frontier molecular orbitals along the intrinsic reaction coordinate and modeled trajectories and examine the correlation between HOMO and LUMO for thermally forbidden systems. We also investigate the electrocyclizations of several highly polarized systems for which the Houk group had predicted that donor-acceptor substitution can induce zwitterionic character, thereby providing low-energy pathways for formally forbidden reactions. We conclude with perspectives on the field of pericyclic reactions, including a refinement as the meaning of Woodward and Hoffmann's "Violations. There are none!" Lastly, we comment on the burgeoning influence of computations on all fields of chemistry.

Cycloaliphatic Quaternary Ammonium Functionalized Poly(oxindole biphenyl) Based Anion-Exchange Membranes for Water Electrolysis: Stability and Performance.

Mechanically robust anion-exchange membranes (AEMs) with high conductivity and long-term alkali resistance are needed for water electrolysis application. In this work, aryl-ether free polyaromatics containing isatin moieties were prepared via super acid-catalyzed copolymerization, followed by functionalization with alkaline stable cyclic quaternary ammonium (QA) cationic groups, to afford high performance AEMs for application in water electrolysis. The incorporation of side functional cationic groups (pyrrolidinium and piperidinium) onto a polymer backbone via a flexible alkyl spacer aimed at conductivity and alkaline stability improvement. The effect of cation structure on the properties of prepared AEMs was thoroughly studied. Pyrrolidinium- and piperidinium-based AEMs showed similar electrolyte uptakes and no obvious phase separation, as revealed by SAXS and further supported by AFM and TEM data. In addition, these AEMs displayed high conductivity values (81. 5 and 120 mS cm-1 for pyrrolidinium- and piperidinium-based AEM, respectively, at 80 °C) and excellent alkaline stability after 1 month aging in 2M KOH at 80 °C. Especially, a pyrrolidinium-based AEM membrane preserved 87% of its initial conductivity value, while at the same time retaining its flexibility and mechanical robustness after storage in alkaline media (2M KOH) for 1 month at 80 °C. Based on 1H NMR data, the conductivity loss observed after the aging test is mainly related to the piperidinium degradation that took place, probably via ring-opening Hofmann elimination, alkyl spacer scission and nucleophilic substitution reactions as well. The synthesized AEMs were also tested in an alkaline water electrolysis cell. Piperidinium-based AEM showed superior performance compared to its pyrrolidinium analogue, owing to its higher conductivity as revealed by EIS data, further confirming the ex situ conductivity measurements.

A theory of the spin-crossover phenomena in the rare earth perovskite LaCoO3 induced by temperature or a magnetic field

Published magnetic data for LaCoO3 are successfully analyzed with coexisting 5 D and low-spin (LS) cobalt states. Energy levels of the two states are derived in analytic forms. To this end, fictitious orbital angular momentum l of magnitude one defines the Γ5 (5 D) state. Our Hamiltonian includes the spin–orbit interaction, and a cubic crystal field embellished by a trigonal distortion . A singlet ground state with an energy gap to the first excited doublet is realized for certain values of the parameters. The temperature-independent paramagnetic susceptibility (TIPS) of the 5 D state has a finite value, which accords with the observation. Whereas, TIPS is symmetry forbidden in the LS state. A rigorous calculation is made of the excitation spectrum in the LS state. The elementary excitation is modeled as a creation of an electron–hole pair that results in an energy level scheme in which the first excited quartet lies above the singlet ground state. The electron spin resonance data are successfully equated with transitions within the excited quartet. Available magnetization data delineate parameters in the 5 D Hamiltonian. The temperature dependence of the susceptibility of our coexisting model is qualitatively reasonable. To improve on a quantitative outcome, we are led to introduce a temperature dependent concentration for the 5 D and LS states. Calculated Bragg diffraction patterns gathered with x-rays tuned to the Co K-edge reveal potential to refine the current crystal structure and to shed light on the origin of the coexisting states.

Singlet Fission in Lycopene H-Aggregates.

A theory of singlet fission (SF) in carotenoid dimers is applied to explain the SF in lycopene H-aggregates observed after high-energy photoexcitation. The explanation proposed here is that a high energy, delocalized bright 1Bu+ state first relaxes and localizes onto a single lycopene monomer. The high-energy intramonomer state then undergoes internal conversion to the 11Bu- state. Once populated, the 11Bu- state allows exothermic bimolecular singlet fission, while its internal conversion to the 21Ag- state is symmetry forbidden. The simulation of SF predicts that the intramonomer triplet-pair state undergoes almost complete population transfer to the intermonomer singlet-pair state within 100 ps. Simultaneously, ZFS interactions begin to partially populate the intermonomer quintet triplet-pair state up to ca. 2 ns, after which hyperfine interactions thermally equilibrate the triplet-pair states, thus forming free single triplets within 50 ns.

Density functional theory study of the styrylbenzoquinoline dyad and the related dibenzoquinolylcyclobutane formed in the [2 + 2] photocycloaddition reaction

AbstractThe structure and electronic properties of the biphotochromic dyad with two styrylbenzo[f]quinoline photochromes, as well as the corresponding cyclobutane with two benzo[f]quinoline (BQ) substituents, are studied by DFT at the M06‐2X/6‐31G* level, the cyclobutane being a product of the [2 + 2] photocycloaddition (PCA) reaction of the dyad. According to calculations, the dyad forms π‐stacked folded conformers, which, when excited, can form excimers that are precursors of cyclobutane. TD DFT calculations and natural transition orbital (NTO) analysis indicated that the lowest singlet excited S1 state in the dyad is localized on the SBQ photochrome, including the ethylene group that undergoes PCA. Thus, the conditions for concerted electrocyclic reactions are satisfied, and the direct PCA follows the Woodward–Hoffmann rules. In contrast, in cyclobutane, the S1 state is localized on the BQ substituent rather than on the cyclobutane core. Therefore, the reverse ring‐opening (retro‐PCA) reaction cannot follow the Woodward‐Hoffmann rules and inevitably involves a step of excitation energy transfer from BQ to cyclobutane, which means the predissociation mechanism.

The Nature of the Chemical Bonds of High-Valent Transition-Metal Oxo (M=O) and Peroxo (MOO) Compounds: A Historical Perspective of the Metal Oxyl-Radical Character by the Classical to Quantum Computations.

This review article describes a historical perspective of elucidation of the nature of the chemical bonds of the high-valent transition metal oxo (M=O) and peroxo (M-O-O) compounds in chemistry and biology. The basic concepts and theoretical backgrounds of the broken-symmetry (BS) method are revisited to explain orbital symmetry conservation and orbital symmetry breaking for the theoretical characterization of four different mechanisms of chemical reactions. Beyond BS methods using the natural orbitals (UNO) of the BS solutions, such as UNO CI (CC), are also revisited for the elucidation of the scope and applicability of the BS methods. Several chemical indices have been derived as the conceptual bridges between the BS and beyond BS methods. The BS molecular orbital models have been employed to explain the metal oxyl-radical character of the M=O and M-O-O bonds, which respond to their radical reactivity. The isolobal and isospin analogy between carbonyl oxide R2C-O-O and metal peroxide LFe-O-O has been applied to understand and explain the chameleonic chemical reactivity of these compounds. The isolobal and isospin analogy among Fe=O, O=O, and O have also provided the triplet atomic oxygen (3O) model for non-heme Fe(IV)=O species with strong radical reactivity. The chameleonic reactivity of the compounds I (Cpd I) and II (Cpd II) is also explained by this analogy. The early proposals obtained by these theoretical models have been examined based on recent computational results by hybrid DFT (UHDFT), DLPNO CCSD(T0), CASPT2, and UNO CI (CC) methods and quantum computing (QC).

Higher-Order Electrocyclizations in Biological and Synthetic Processes.

In general, electrocyclizations follow the Woodward-Hoffmann's rules of conservation of orbital symmetry. These rules have been extensively verified in low-order processes, both in thermal and photochemical reactions, up to eight π-electrons. However, when the number of π-electrons in the system increases, some deviations of that general rules can be found. This focused review highlights the main features of reported higher-order electrocyclizations involving 10, 12, 14, 16 and 18 π-electrons. Some of these examples constitute useful intermediates in the synthesis of biologically active compounds. When computational studies were not included in the reported examples, DFT calculations have been performed to be included in this review. Analysis of the respective pericyclic topologies shows the importance of computational tools for understanding the selectivity observed experimentally.

The Electrocyclization of Heptatrienyl Anions

AbstractThe thermal electrocyclization of heptatrienyl anions is reviewed. We begin with a succinct background on the importance of cycloheptane rings in complex molecules and a brief survey of approaches to their synthesis. We also review the fundamental aspects of this electrocyclization manifold, relying on the Woodward–Hoffmann rules for pericyclic chemistry. Then we survey the literature, covering the burst of discovery in the late 1960s and early 1970s, and the more sporadic reports in from the 1990s to the present day.1 Introduction2 The Electrocyclization of Heptatrienyl Anions3 Discovery and Early Development (1964–1975)4 Recent Developments (1996–2023)5 Concluding Remarks