Benzyl Alcohol Research Articles

Configuration Effect of Plasmonic Vanadium–Titanium Solid Solutions for Photo-oxidation of Benzyl Alcohol

Configuration Effect of Plasmonic Vanadium–Titanium Solid Solutions for Photo-oxidation of Benzyl Alcohol

Stereoselective Single Step Cyclization to Give Belt-Functionalized Pillar[6]arenes.

Two macrocycles were synthesized through cyclization reactions of secondary benzylic alcohols, giving pillar[6]arenes with a methyl substituent at each belt position. These macrocycles form stereoselectively with only the rtctct isomer with alternating up and down orientations of the belt methyl groups definitively identified. Isolated yields were modest (7 and 9%), but the macrocycles are prepared in a single step from either a commercially available alcohol or a very readily prepared precursor. X-ray crystal structures of the macrocycles indicate they have a capsule-like structure, which is far from the conventional pillar shape. Density functional theory calculations reveal that the energy barrier required to obtain the pillar conformation is significantly higher for these belt-functionalized macrocycles than for conventional belt-unfunctionalized pillar[6]arenes.

Transition metal modified Al2O3 mesoporous nanospheres for catalysis of organic reactions

The performance of metal oxide-based catalysts are usually determined by their characteristics such as material composition, morphology, and surface/interface properties. Therefore, rational design of metal oxide-based catalysts with special surface/interface characteristics and porous microstructure still needs further research. In this work, a facile two-step solvothermal-annealing method is developed for the synthesis of transition metal (TM) modified Al2O3 (TM-Al2O3, TM = Cu, Fe, Ni, Co) nanospheres. The influences of different ratios of solvents (e.g., water and glycerol) on the morphology and particle size of the nanocatalysts are explored. Benefitting from the nano-spherical morphology and unique mesoporous structure, the representative catalyst (i.e., Cu-Al2O3) exhibits favorable catalytic performance in 4-nitrophenol reduction and benzyl alcohol oxidization reactions. The turnover frequency of Cu-Al2O3 is high up to 35.9 min−1 for the reduction of 4-nitrophenol, which is higher than that of its counterparts (i.e., Fe-Al2O3, Ni-Al2O3, and Ni-Al2O3) and many recently reported Al2O3-based catalysts. Moreover, the pH of the reaction system is regulated to enhance the catalytic efficiency in selective oxidization of benzyl alcohol by an additive addition strategy. These results suggest that the nano-spherical and mesoporous morphology is indeed effective for the activity enhancement of TM-Al2O3 catalysts. The same catalyst designing concept and performance regulation strategy may be extended to other TM-modified metal oxide systems, making it possible to tune the catalytic behavior for various chemical reactions.

Atomically Dispersed Iron Active Sites on Covalent Organic Frameworks for Artificial Photosynthesis of Hydrogen Peroxide

AbstractArtificial photosynthesis has been regarded as a promising solution toward solar energy conversion, generating storable and transportable chemical fuels such as hydrogen (H2) and hydrogen peroxide (H2O2). However, the design of robust catalytic sites not only affects the activity, but also identify the atomic‐level correlation between active sites and natural photosynthesis performance. Herein, a synthesis method of single‐atomic Iron (Fe) active sites anchored on novel covalent organic framework (COF) for the production of H2O2 under visible light irradiation. When benzyl alcohol is the most sacrificial agent, the state‐of‐the‐art Fe‐based COF exhibits an excellent H2O2 generation rate of 4130 µmol g−1 h−1, over 5.3 times higher than that of pristine COF, achieving an apparent quantum yield of 6.4% at 420 nm. The enhanced photocatalytic performance is ascribed to the synergistic effect of atomically dispersed Fe sites and COF hosts, reducing the reaction energy barrier for the formation of *OOH intermediates and optimizing the adsorption of O2 and thus promoting two‐electron oxygen reduction reaction (ORR). This work establishes an atomic‐level engineering approach to build atomically dispersed Fe active sites on COF photocatalysts and provides in‐depth insight upon the ORR mechanism for promising artificial photosynthesis of H2O2.

Noninnocent Azo-Aromatic Cobalt(II)-Catalyzed sp3 C-H Alkylation of Fluorenes with Alcohols.

Herein, employing well-defined redox noninnocent cobalt(II) complexes an efficient sp3 C-H alkylation of fluorenes using alcohols as alkylating agents to result in alkylated fluorenes is reported. The catalytic protocol was versatile with various fluorenes and benzyl alcohols. It also showed very good functional group tolerance with both alcohols and fluorenes. Moreover, an efficient single-step and simultaneous di C-C as well as both C-C and the C-N alkylation reaction of fluorenes was observed with this catalytic protocol. Such selective single-step dialkylation of fluorenes is indeed beneficial. Several control experiments, deuterium labeling, and 1H NMR kinetic studies have revealed a ligand radical-based borrowing hydrogen mechanism involving the azo-aromatic complexes of cobalt as catalysts for the alkylation of fluorenes.

Volatiles from nutritional fungal symbiont influence the attraction of Anisandrus maiche (Coleoptera: Curculionidae) to ethanol-baited traps.

Anisandrus maiche Stark (Coleoptera: Curculionidae: Scolytinae) is a non-native ambrosia beetle from central Asia that has been spreading throughout the eastern United States since 2005. Preferred hosts of A. maiche are not well characterized within its currently invaded range, but it is established in managed and natural forests throughout Indiana. Current monitoring and detection efforts for this beetle rely on ethanol-baited traps, but fungal volatiles may alter the attraction of A. maiche to ethanol. In this study, we conducted trapping experiments in Indiana to determine the extent to which a suite of common fungal alcohols influences the response of A. maiche to ethanol-baited traps. We then evaluated isoamyl and isobutyl alcohol as potential attractants for A. maiche and their ability to enhance attraction to ethanol. Lastly, we used SPME-GC-MS to identify volatiles from Ambrosiella cleistominuta (Mayers & Harr.), the fungal symbiont of A. maiche, grown for 7 and 14 days on malt extract agar. Benzyl alcohol, isobutyl alcohol, hexanol, methyl phenylacetate, phenethyl alcohol, and piperitone reduced the attraction of A. maiche to ethanol-baited traps in the field. Moreover, adding methyl benzoate and isoamyl alcohol individually to ethanol-baited traps did not further increase A. maiche capture. When paired with ethanol, isoamyl alcohol repelled beetles in the early flight period but did not significantly increase trap capture during the fall flight. These results represent a first step in understanding the role of fungal volatiles in the colonization behavior of A. maiche and may ultimately inform management strategies for this species.

Benzyl alcohol, benzyl benzoate and methyl benzoate as bio-insecticides against dried bean beetle Acanthoscelides obtectus (Coleoptera: Tenebrionidae)

Acanthoscelides obtectus is most dangerous pest of preserved beans. The current study used benzyl alcohol (BA), benzyl benzoate (BB), and methyl benzoate (MB) to control A. obtectus. Contact and fumigant toxicity tests were performed to evaluate the efficacy of the used compounds. The contact toxicity assay revealed a significant mortality rate with LC50 reached at low concentrations of 0.57, 0.68, and 0.94 μL/g for BA, BB, and MB, respectively. BA possesses significant fumigant toxicity and outperforms MB and BB, with an LC50 achieved at concentration of 8.91 μL/L. In comparison to the control group, BA, BB, and MB have anti-feedant efficacy against A. obtectus. Furthermore, even at a low concentration of 0.5 μL/g, these compounds induced a significant suppression of A. obtectus F1 progeny production. The BA and BB activities persisted until day 5 after treatment while MB activity sustained for 3 days only. These compounds significantly inhibited acetylcholinesterase, decrease in the level of reduced glutathione (GSH), and elevated malondialdehyde (MDA). In conclusion, BA, BB, and MB are particularly promising choices for controlling the bean beetle A. obtectus because they are low in cost, of natural origin, and the European Food Safety Authority (EFSA) approved their use in animal feed.

Tailoring the catalytic sites by regulating photogenerated electron/hole pairs separation spatially for simultaneous selective oxidation of benzyl alcohol and hydrogen evolution

Photocatalytic selective oxidation of alcohols into aldehydes and H2 is a green strategy for obtaining both value-added chemicals and clean energy. Herein, a dual-purpose ZnIn2S4@CdS photocatalyst was designed and constructed for efficient catalyzing benzyl alcohol (BA) into benzaldehyde (BAD) with coupled H2 evolution. To address the deep-rooted problems of pure CdS, such as high recombination of photogenerated carriers and severe photo-corrosion, while also preserving its superiority in H2 production, ZnIn2S4 with a suitable band structure and adequate oxidizing capability was chosen to match CdS by constructing a coupled reaction. As designed, the photoexcited holes (electrons) in the CdS (ZnIn2S4) were spatially separated and transferred to the ZnIn2S4 (CdS) by electrostatic pull from the built-in electric field, leading to expected BAD production (12.1 mmol g−1 h−1) at the ZnIn2S4 site and H2 generation (12.2 mmol g−1 h−1) at the CdS site. This composite photocatalyst also exhibited high photostability due to the reasonable hole transfer from CdS to ZnIn2S4. The experimental results suggest that the photocatalytic transform of BA into BAD on ZnIn2S4@CdS is via a carbon-centered radical mechanism. This work may extend the design of advanced photocatalysts for more chemicals by replacing H2 evolution with N2 fixation or CO2 reduction in the coupled reactions.

Atroposelective Synthesis of 2‐(Quinolin‐8‐yl)benzyl Alcohols by Biocatalytic Dynamic Kinetic Resolutions

AbstractA highly enantioselective biocatalytic dynamic kinetic resolution (DKR) of 2‐(quinoline‐8‐yl) 3‐methylbenzaldehydes and 1‐naphthaldehydes is described. The reaction proceeds by atroposelective carbonyl reduction catalyzed by commercial ketoreductases (KREDs), generally reaching high conversions and excellent enantiomeric excesses. Both atropoisomers of the final alcohols can be obtained by a proper selection of the biocatalyst. The DKR strategy relies in the racemization of the stereogenic axis that takes place thanks to a transient Lewis acid‐base interaction (LABI) between the nitrogen in the quinoline and the carbonyl group.

Systematic engineering enables efficient biosynthesis of L-phenylalanine in E. coli from inexpensive aromatic precursors

BackgroundL-phenylalanine is an essential amino acid with various promising applications. The microbial pathway for L-phenylalanine synthesis from glucose in wild strains involves lengthy steps and stringent feedback regulation that limits the production yield. It is attractive to find other candidates, which could be used to establish a succinct and cost-effective pathway for L-phenylalanine production. Here, we developed an artificial bioconversion process to synthesize L-phenylalanine from inexpensive aromatic precursors (benzaldehyde or benzyl alcohol). In particular, this work opens the possibility of L-phenylalanine production from benzyl alcohol in a cofactor self-sufficient system without any addition of reductant.ResultsThe engineered L-phenylalanine biosynthesis pathway comprises two modules: in the first module, aromatic precursors and glycine were converted into phenylpyruvate, the key precursor for L-phenylalanine. The highly active enzyme combination was natural threonine aldolase LtaEP.p and threonine dehydratase A8HB.t, which could produce phenylpyruvate in a titer of 4.3 g/L. Overexpression of gene ridA could further increase phenylpyruvate production by 16.3%, reaching up to 5 g/L. The second module catalyzed phenylpyruvate to L-phenylalanine, and the conversion rate of phenylpyruvate was up to 93% by co-expressing PheDH and FDHV120S. Then, the engineered E. coli containing these two modules could produce L-phenylalanine from benzaldehyde with a conversion rate of 69%. Finally, we expanded the aromatic precursors to produce L-phenylalanine from benzyl alcohol, and firstly constructed the cofactor self-sufficient biosynthetic pathway to synthesize L-phenylalanine without any additional reductant such as formate.ConclusionSystematical bioconversion processes have been designed and constructed, which could provide a potential bio-based strategy for the production of high-value L-phenylalanine from low-cost starting materials aromatic precursors.

Chitosan-derived mesoporous N-doped carbon catalyst embedded with NiO for highly selective benzyl alcohol oxidation

MOF-derived heteroatom-doped mesoporous carbons have gained the significant consideration in heterogenous catalytic reactions because of their multipurpose features. Especially, the high Specific Surface Area (SSA) of these materials provides abundant activated sites for the catalytic reactions, while the mesoporous structure allows for the effective mass transfer, enhancing the overall capability of the catalytic process. Herein, the efficient NiO/CN-T (T referred to the pyrolysis temperature) was prepared by facile pyrolysis of MOF/CS composite (Ni-MOF (74), Chitosan) in the presence of excess amount of starch as the carbon precursor. The NiO/CN-T as heterogenous catalyst has desired SSA varied from 1094 to 491 m2.g−1. The optimized catalyst (NiO/CN-600) possesses the superior catalytic activity toward the oxidation of the BnOHs due to its high SSA (1094 m2.g−1), which can notably rectify the mass transfer proficiency. Additionally, the NiO/CN-600 heterogenous catalyst also represents the acceptable chemical stability. So, it was demonstrated that such an innovative strategy can provide several versatile tunability insights for the preparation of MOF/biopolymer-derived heterogenous catalysts.

Urinary benzyl alcohol and hippuric acid in workers exposed to benzyl alcohol during paint-stripping work.

We aimed to develop a reliable gas chromatography-mass spectrometry (GC-MS) method for detecting urinary benzyl alcohol (BeOH) concentrations and assess the suitability of urinary BeOH as a biomarker for occupational BeOH exposure. Thirteen male participants exposed to BeOH during paint-stripping work provided preshift and postshift urine samples, and their personal exposure concentrations were measured. Meanwhile, a control group of 10 nonexposed workers contributed urine samples. The newly developed GC-MS method met regulatory guidelines. The personal exposure concentrations of BeOH ranged from 8.4 to 45.2mg/m3. Postshift urine samples from exposed participants showed significant BeOH and hippuric acid (HA) concentration increases compared with preshift samples (BeOH, post-/pre-shift geometric mean [GM] ratio = 7.5-7.8, P < .001; HA, post-/pre-shift GM ratio = 4.3-4.5, P < .001). These levels were considerably higher than those in postshift samples from the nonexposed control group (BeOH, exposed-/nonexposed-workers GM ratio = 14.8-19.0, P < .001; HA, exposed-/nonexposed-workers GM ratio = 12.1-15.3, P < .001), even after urine density correction. Urinary BeOH and HA can serve as potential biomarkers of occupational exposure to BeOH. More specifically, BeOH might serve as a biomarker superior to HA because it is apparently less influenced by confounding factors such as dietary intake and genetic polymorphism of low-Km aldehyde dehydrogenase (ALDH2). The findings will improve workplace safety measures and protocols, assisting health care professionals in diagnosing and managing exposure-related health issues, thereby potentially reducing the risk of occupational exposure to BeOH.

Green, Solvent-Free Mechanochemical Synthesis of Nano Ag2O/MnO2/N-Doped Graphene Nanocomposites: An Efficient Catalyst for Additive-Base-Free Aerial Oxidation of Various Kinds of Alcohols.

Herein, we report a solvent-less, straightforward, and facile mechanochemical technique to synthesize nanocomposites of Ag2O nanoparticles-doped MnO2, which is further codoped with nitrogen-doped graphene (N-DG) [i.e., (X %)N-DG/MnO2-(1% Ag2O)] using physical milling of separately prepared N-DG and Ag2O NPs-MnO2 annealed at 400 °C over an eco-friendly ball-mill process. To assess the efficiency in terms of catalytic performance of the nanocomposites, selective oxidation of benzyl alcohol (BlOH) to benzaldehyde (BlCHO) is selected as a substrate model with an eco-friendly oxidizing agent (O2 molecule) and without any requirements for the addition of any harmful additives or bases. Various nanocomposites were prepared by varying the amount of N-DG in the composite, and the results obtained highlighted the function of N-DG in the catalyst system when they are compared with the catalyst MnO2-(1% Ag2O) [i.e., undoped catalyst] and MnO2-(1% Ag2O) codoped with different graphene dopants such as GRO and H-RG for alcohol oxidation transformation. The effects of various catalytic factors are systematically evaluated to optimize reaction conditions. The N-DG/MnO2-(1% Ag2O) catalyst exhibits premium specific activity (16.0 mmol/h/g) with 100% BlOH conversion and <99.9% BlCHO selectivity within a very short interval. The mechanochemically prepared N-DG-based nanocomposite displayed higher catalytic efficacy than that of the MnO2-(1% Ag2O) catalyst without the graphene dopant, which is N-DG in this study. A wide array of aromatic, heterocyclic, allylic, primary, secondary, and aliphatic alcohols have been selectively converted to respective ketones and aldehydes with full convertibility without further oxidation to acids over N-DG/MnO2-(1% Ag2O). Interestingly, it is also found that the N-DG/MnO2-(1% Ag2O) can be efficiently reused up to six times without a noteworthy decline in its effectiveness. The prepared nanocomposites were characterized using various analytical, microscopic, and spectroscopic techniques such as X-ray diffraction, thermogravimetric analysis, Fourier-transform infrared spectroscopy, Raman, field emission scanning electron microscopy, and Brunauer-Emmett-Teller.

Palladium-based pseudohomogeneous catalyst for highly selective aerobic oxidation of benzylic alcohols to aldehydes

This study presents a novel class of pseudohomogeneous catalysts (PHC) based on carbon quantum dots functionalized with terpyridine ligands (CQDs-Tpy) to immobilize and stabilize palladium nanoparticles (Pd NPs). Extensive characterization techniques clearly confirmed the successful stabilization of Pd NPs on CQDs-Tpy. The effectiveness of the catalyst was demonstrated in the selective aerobic oxidation of primary and secondary of benzylic alcohols to aldehydes in the absence of additives and phase transfer catalyst (PTC). Remarkably, the reactions predominantly yielded aldehydes without further oxidation to carboxylic acids. By employing low catalyst loadings (0.13 mol%), high conversions (up to 89%) and excellent selectivity (> 99%) of the aldehyde derivatives were achieved. Moreover, the CQDs-Tpy/Pd NPs catalyst displayed suitable catalytic activity and recyclability, offering potential economic advantages. This promising approach opens up new opportunities in the field of catalysis for designing subnanometric metal-based PHCs.

Exploring the Intricacies and Functionalities of Galactose Oxidase: Structural Nuances, Catalytic Behaviors, and Prospects in Bio-electrocatalysis

Galactose Oxidase, also known as GOase, is an enzyme found mostly in Fusarium graminearum, Dactylium dendroides, and Gibberella fujikuroi. GOase, containing copper, serves catalytic functions in oxidizing substrates and primary alcohols such as d-galactose, benzyl alcohol derivatives, and dihydroxyacetone. The catalytic property of galactose oxidase that differentiates it from other enzymes is its cofactor consisting of a Cu (II)-bound Cys-Tyr* radical. The cofactor is vital for enabling regioselective oxidation. The application of galactose oxidase (GOase) covers several fields such as enzymatic synthesis, biosensors development, and processes of diagnosis.&#x0D; Galactose oxidase (GOase) was discovered to have a crystallographic structure by X-ray diffraction, which revealed an active site containing copper ions displaying relatively square pyramidal geometry. There are three unique structural and functional domains of the enzyme GOase. The domains include Tyr495 and a covalent bond between Cys228 and Tyr272 serving as equatorial and axial ligands, respectively. The mechanism of catalysis covers three different oxidation states, which include the active state containing Cu (II)-radical, the intermediate state containing Cu (II)-tyrosine, and the Cu(I)-tyrosine state. The cycle of catalysis that has been posited comprises several phases which are: (i) substrate binding, (ii) the transfer of proton (iii) the transfer of hydrogen atom, and (iv) subsequent oxidation steps. These phases eventually yield the synthesis of aldehyde and hydrogen peroxide.&#x0D; Galactose oxidase’s (GOase) mechanism of catalysis has been studied thoroughly via extensive research focusing on explaining the ping-pong mechanism that occurs in both oxidative and reductive half-reactions. The processes of activating and reactivating galactose (GOase) involve the transfer of electrons in which horseradish peroxidase (HRP) serves as an activator. The electrochemical investigations provide evidence of the electrochemical activation and reactivation of GOase in the presence of mediators.&#x0D; This comprehensive review enhances the comprehension of the structural complexities, catalytic mechanisms, and bio-electrocatalytic potential of GOase, thereby establishing a basis for future investigations and developments in technology.

Controlling achiral and chiral conformations of benzyl alcohol by ortho-halogenation, collisional relaxation and dimerisation.

Ortho-Halogenated benzyl alcohol can exist in two different low energy chiral conformations, only one of them with an OH-X contact (X = Cl, Br, I). A third, achiral conformation is enabled by the halogen substitution. We show by IR spectroscopy in supersonic jets that the achiral monomer is less stable than the chiral conformation with OH-X contact, but both can be produced in similar amounts using helium as a carrier gas. The robust OH transition observed for the achiral monomer is a sensitive benchmark for the conformational energy sequence, since the chiral conformation without OH-X contact is at least an order of magnitude less abundant, although it is often predicted by DFT to be slightly more stable and separated from the achiral conformation by a low barrier. This competing chiral conformation must be energetically higher by at least a few tenths of a kJ mol-1 to be consistent with experimental observations. That is indeed predicted by high-level energy calculations at the DFT-optimised structures. The most stable dimers of ortho-halogenated benzyl alcohols involve torsionally homo- and heterochiral pairings of the two OH groups, where the hydrogen bond-accepting OH group forms a cooperative intramolecular OH-X contact. The achiral monomer conformation is suppressed in these dimers. A homochiral dimer is formed almost exclusively for Cl, whereas its heterochiral variant is progressively co-stabilised with increasing halogen size. The stretching wavenumber of the donor OH in the dimers depends on the relative chirality of the donor and acceptor conformations. The consistent picture that emerges for Cl, Br and I substitution in ortho-position of benzyl alcohol is discussed in the context of interconversion barriers, heavy atom tunneling, π-π stacking, suppression of OH-π bonding, chirality synchronisation, and shortcomings of DFT approaches in reproducing the observations. The homochiral aggregation preference observed for simple benzyl alcohol is conserved and even enhanced upon ortho-halogenation, albeit partly by different interactions.

Selective photocatalytic C-C coupling of benzyl alcohol into hydrobenzoin using Pt-deposited CdS nanosheets passivated with cysteamine.

Achieving high selectivity towards hydrobenzoin (HB) from photocatalytic carbon-carbon (C-C) coupling reaction of benzyl alcohol (BzOH) remains a challenge due to side competing reactions and subsequent conversions of HB into its derivatives. In this study, we have developed a high-performance CdS-based photocatalyst for synthesizing HB with precisely controlled surface properties and structure, achieving high selectivity for HB synthesis. We employed strategies such as cysteamine passivation and Pt deposition to address issues related to photogenerated charge trapping and recombination, thereby enhancing the photocatalytic capability of CdS. With optimized Pt/CdS NSs as the photocatalyst, we investigated the impact of the Pt/CdS heterostructure on intermediate reactions, which in turn altered product selectivity. Specifically, excessive Pt suppresses the electron-induced benzaldehyde-to-intermediate reaction by consuming electrons for the competing hydrogen evolution reaction (HER), leading to high selectivity toward benzaldehyde. In contrast, bare CdS without Pt suffers from insufficient charge supply for BzOH conversion due to the charge recombination issue, which promotes the subsequent conversion of HB to its derivatives. Notably, when Pt is precisely loaded to avoid dominant HER competition, the overall reaction rate increases, maintaining high selectivity towards HB and ensuring faster conversion of BzOH to HB rather than subsequent conversions of HB into its derivatives, thereby maximizing the HB yield. Subsequently, we have developed a photocatalyst that achieves a 93.4% conversion of 0.24 mmol BzOH with 85.3% selectivity toward HB under solar simulator irradiation (AM 1.5G). This work is expected to offer instructive guidance on rationally designing the photocatalyst for efficient C-C coupling reactions.

Complete depolymerization of poly(ester-alt-thioether)s under mild conditions into AB functional monomers

Full depolymerization of functional poly(ester-alt-thioether)s by methanolysis at room temperature and subsequent step-growth repolymerization.

Ni-Co hexacyanoferrate hollow nanoprism with CN vacancy for electrocatalytic benzyl alcohol oxidation.

An innovative method to improve the oxidation efficiency of benzyl alcohol utilizes Ni-Co hexacyanoferrate hollow nanoprisms. Synthesized via a gentle self-sacrificial template method, this catalyst exhibits substantial catalytic activity and selectivity towards benzyl alcohol oxidation, facilitated by the strategic incorporation of Co to modulate CN vacancy density. Impressively, it achieves a current density of 10 mA cm-2 at 1.33 V and a remarkable 98% efficiency in benzyl alcohol conversion at 1.4 V.

Copper(II) quinoxolinol imidazolium complexes in catalytic oxidation of benzylic and heterocyclic alcohols.

A novel copper(II) quinoxolinol complex has been prepared using a condensation reaction based on previous studies. The copper(II) quinoxolinol salen complex has been applied as a catalyst using tert-butyl hydroperoxide (TBHP) as the oxidant, demonstrating that benzylic and heterocyclic alcohols can be converted efficiently to the corresponding aldehydes. Excellent yields can be achieved (up to 99%) within a short reaction time and with great tolerance for functional groups.