Acetophenone Research Articles

Effective breaking of β-o-4 bonds in lignin model compounds by g-C3N4/ZnIn2S4 photocatalyst under visible light

In this study, cauliflower-like g-C3N4/ZnIn2S4 composite photocatalysts were prepared via a hydrothermal method by loading ZnIn2S4 on g-C3N4 nanosheet layers. The crystal structures of the prepared samples were characterized by X-ray diffractometer. TEM and XPS characterization indicated the successful catalyst compounding, while PL and UV–Vis-DRs characterization illustrated the broadening of the visible light absorption interval of g-C3N4/ZnIn2S4 and the low photogenerated electron-hole complexation rate. The lignin model compounds were degraded under visible light, and the GC-MS analysis of the composition of the products showed that CN/ZIS-15 degraded, with 94 % conversion of 2-phenoxy-1-phenylethanol(PP-ol) in 3 h, which was 2.5 times higher than that of pure g-C3N4, and the main products being acetophenone (AP) and phenol (Phol). The reactive radical trapping experiments were carried out to investigate the main reactive species in the reaction and to explore the mechanism for the breaking of β-O-4 bond.

Supported copper nanoarchitecture for selective ethylbenzene oxidation (EBO) reaction

Copper-based (Cu-NP) uniformly dispersed on various inorganic supports (alumina, silica, titania, and zirconia) were prepared by the reverse microemulsion technique. These nanoparticles were used for the selective oxidation of ethylbenzene (EB) to produce acetophenone (AP) as the main product in the presence of Tert‑butyl hydroperoxide(TBHP) as an oxidant. This study focused on creating Cu-nanoparticles evenly dispersed on alumina using varying Cu-loadings (5 %, 10 %, and 15% wt.) and Brij-35 as the surfactant. The resulting catalytic material was characterized using various physicochemical techniques like XRD, FESEM, HRTEM, XPS and physisorption techniques. Various parametric studies were conducted, such as the effects of temperature, catalyst support, catalyst loading, and TBHP loading to optimize the EB conversions and AP selectivity. Among the various catalyst loadings, 15 % CuO/Al2O3 (15 % of the copper content) nanocomposites showed exceptional performance, with the highest EB conversion rate (99.7 %) and AP selectivity (98.5 %) compared to other nanocomposites. The catalyst's stability and recyclability over four cycles were attributed to the strong copper oxide-alumina interaction. These findings suggest that this nanocomposite material is a promising candidate for catalytic applications, offering high selectivity and consistent EB conversion rates.

Manipulation of Electronic Effect and Assembly Architecture to Invoke Oxidation of Ethylbenzene by Hierarchical Co3O4 Wreaths.

A high-performance transition-metal oxide catalyst can be designed by appropriately integrating the concepts of morphology regulation and electronic structure modulation. In this work, hierarchical Co3O4 wreaths (CCW) enriched with oxygen vacancies (Ov) were facilely constructed for the selective oxidation of ethylbenzene (EB) to acetophenone (AP). Under the screened optimal reaction conditions, the CCW catalyst can offer a 79.1% conversion of EB (ri = 0.244 mol gcat-1 h-1) accompanied by a selectivity of 92.3% to AP. The good reaction performance can be attributed to the cooperation of defect engineering and architecture design, which can synergistically facilitate the EB oxidation performance by augmenting the intrinsic reactivity and accessibility of active sites. This work presents a reliable route to construct a high-performance transitional metal oxide catalyst via manipulation of electronic effect and assembly architecture for the selective oxidation of EB and beyond.

Advanced analysis of the adsorption mechanism for sweet odorant on mouse and human olfactory receptors via statistical physics theory

In this work, the one layer statistical physics model (M1) was applied to more deeply comprehend the phenomenon of adsorption, which is putatively involved in the olfactory sensation of acetophenone (AP) on mouse and human olfactory receptors. On one hand, the proposed model was utilized to microscopically characterize the studied olfactory systems in order to obtain advanced stereographic and energetic information concerning the studied olfactory systems in terms of a molecular view point. Based on the values of the number of acetophenone molecules docked on mouse and human binding sites n, it was found that the studied sweet odorant was linked with a mixed orientation. Energetically speaking, the values of the molar adsorption energy ΔE1, which ranged from 11.81 to 17.67 kJ/mol for mouse olfactory receptors (Olfr62, Olfr1093, Olfr1094, Olfr895, and Olfr876) and from 14.66 to 20.58 kJ/mol for human olfactory receptors (OR2C1, OR1A1, and OR2J2), indicated that acetophenone molecules were exothermically physisorbed. The adsorption energy distributions relative to AP may also be estimated to understand the olfactory sense in the investigated olfactory systems via the calculation of olfactory bands (i. e., AED bands), which may be defined between 4.80 and 27 kJ/mol and between 5.50 and 27 kJ/mol for mouse and human olfactory receptors, respectively. On the other hand, M2 was used to determine three thermodynamic potentials (i.e., the internal energy, the Gibbs free energy, and the adsorption entropy), which macroscopically characterized the investigated olfactory systems via a detailed thermodynamic analysis of the different olfactory systems.

Coupled Interface and Oxygen-Defect Engineering in Co3O4/CoMoO4 Heterostructures toward Active Oxidation of Ethylbenzene.

The catalytic oxidation of ethylbenzene (EB) is a promising route to produce acetophenone (AcPO). Unfortunately, it remains a great challenge to achieve the highly efficient oxidation of EB under solvent-free conditions using molecular oxygen as the sole oxidant. In this contribution, we present a facile strategy to construct hierarchical oxygen vacancy-rich Co3O4/CoMoO4 heterostructures (Vö-CCMO), which delivers a high yield value of 74.5% at 83.2% conversion of EB and selectivity of 89.6% to AcPO. Both experimental studies and theoretical calculations substantiate the important role of oxygen-defect engineering triggered by the modified chemistry environment at the interfaces between the biphasic phases, which contributes to the good catalytic performance. This work illustrates a promising paradigm for the exploit of advanced catalysts toward boosting EB oxidation reaction in a more practical way.

Green and efficient catalytic oxidation of ethylbenzene to acetophenone over cobalt oxide supported on a carbon material derived from sugar.

The use of biomass as a carbon source to support metal oxides has significant advantages in environmental protection and reducing the cost of the catalyst. The critical point lies on the development of highly active and recyclable catalysts. In this study, sugar was used as a carbon source, and cobalt oxide was loaded via an in situ method and an impregnation method to prepare the catalyst, respectively. The catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR) spectroscopy, Raman, in situ electron paramagnetic resonance (in situ EPR) and N2 adsorption-desorption. The characterization results show that the macroporous carbon-supported cobalt oxide catalyst prepared by the in situ method contains CoOx nanoparticles on the support, but the dispersion of cobalt oxide on the support is more uniform compared with the catalyst prepared by the impregnation method. The catalytic performance of the prepared catalyst was evaluated through the oxidation of ethylbenzene (EB) to acetophenone (AP) as a probe reaction. Under the optimized reaction conditions, temperature (T) = 80 °C, m(catalyst) : m(EB) = 0.15, n(H2O2) : n(EB) : n(KBr) = 14.4 : 1 : 0.1, t = 8 h, and V(EB) : V(CH3COOH) = 1 : 10, the conversion of EB and the selectivity of AP were 84.1% and 81.3%, respectively. CoOx/SC-10-in situ exhibits improved reactivity of EB oxidation owing to cobalt ions on the carbon support that promote the free radical and acid catalytic reaction pathway. The cobalt oxide catalyst supported by biomass carbon has decent recycling and regeneration ability, which provides a new idea for the application of biomass.

A SOLVENT FREE GREEN APPROACH FOR THE SYNTHESIS OF 1,3,5-TRIARYLBENZENES UNDER SULPHATED TIN OXIDE(SO4 2-/SnO2) CATALYST

The efficient and promising solvent-free method, catalyzed by Sulphated Tin oxide (SO4 2-/SnO2), has been developed for the synthesis of 1,3,5-triarylbenzene and its derivatives. The Bronsted acidic surfactant catalyst facilitates quick results and high yields, offering additional advantages such as easy separation and reusability with almost the same efficiency for subsequent cycles. This protocol involves the self-condensation of three molecules through cyclotrimerization with high chemo-selectivity. The substrate methyl phenyl ketone contains both electronwithdrawing and electron-donating groups, which assemble the target moiety with high and low yields, respectively. The synthesized compounds are evaluated through in silico studies to assess their drug-likeness properties.

Expediting Ethylbenzene Oxidation via a Bimetallic Cobalt-Manganese Spinel Structure with a Modulated Electronic Environment.

The catalytic oxidation of ethylbenzene (EB) into acetophenone (AP) is a vibrant area, with a growing number of researchers paying attention to this thematic investigation. Herein, we demonstrate that spinel-type (Co,Mn)(Co,Mn)2O4 can function as an efficient catalyst for the solvent-free oxidation of EB with molecular oxygen. The incorporation of Mn into the Co3O4 network can break the local structural symmetry of Co-O-Co linkages due to the bond competition, inducing the formation of an asymmetrical Co-O-Mn configuration with an electron local exchange interaction. The Co-O-Mn sites can facilitate the perturbation of nonpolar O2 and thus contribute to the generation of abundant •O2- species for initiating the oxidation of EB. We envision that this study not only provides a promising catalyst for EB oxidation but also affords a new insight into the design of advanced spinel oxides for selective oxidation reactions.

Insights into ethylbenzene oxidation catalyzed by transition-metal oxides: Crucial role of hydroperoxide transformation

Selective oxidation of aromatics via a free-radical process is a crucial ingredient in the chemical industry, in which the transformation of hydroperoxide was considered the key step to facilitate the reaction. In this study, the aerobic oxidation of ethylbenzene (EB) to acetophenone (AcPO) catalyzed by carbon nitrides (CNx) supported the transition-metal oxides was performed. Among these catalysts, Co3O4/CNx displayed the highest activity with 48.09 % EB conversion and 77.8 % AcPO selectivity, due to the efficient decomposition of 1-phenylethyl hydroperoxide (PEHP). Notably, in the case of CuO/CNx, the relatively low EB conversion (19.8 %) and high selectivity of AcPO (70.2 %) were observed, while almost no PEHP was detected. Further mechanism investigations revealed that the decomposition of hydroperoxide over CuO/CNx was too fast to generate the reactive free-radicals, which could not efficiently facilitate the propagation steps. Moreover, the addition of tert-butyl hydroperoxide (TBHP) participated in the α-H abstraction of EB and facilitated of radical propagation, showing the distinguished activities over Co3O4/CNx and CuO/CNx.

Synthesis of flower-shaped cyclodextrin microporous organic networks for selective recovery of acetophenone and 1-phenylethanol from petrochemical effluents

Fabrication of efficient and renewable biomass-derivatives-based porous materials with large surface area, good stability and selectivity for recovering acetophenone (AP) and 1-phenylethanol (PE) from petrochemical by-products is of great significance and challenge. In this work, nine novel cyclodextrins-based microporous organic networks (CD-MONs) are designed and synthesized by choosing various CD-based building blocks and aromatic alkynes. Among them, a flower-shaped DEB-γ-CD-MON not only retains the cage-type cavity and the high density of hydroxyl sites within γ-CD, possesses the large surface area, outstanding chemical robustness and strong hydrophobicity, but also offers high AP adsorption capacity (1.93 mmol g−1), good AP/PE selectivity (8.1), and recycle stability both in batch and continuous adsorption modes. The experimental and theoretical results indicate that the hydrogen bonding, π-π stacking and van der Waals interaction between adsorbents and adsorbates are favorable for binding AP toward PE. This work not only provides a biomass-derivatives-based adsorbent for the separation and recovery of AP and PE from PO/SM waste effluent, but also breaks the limitation of the original structure and characteristic of natural biomass to realize added value in biomass valorization.

N-doped hollow carbon nanospheres anchored Pd NPs for mild selective hydrodeoxygenation of bio-models

Hydrodeoxygenation (HDO) is a promising approach for the synthesis of renewable fuels and chemicals, while the design and preparation of high-performance catalysts in this field remain a challenge. Herein, a series of hollow carbon nanospheres anchored Pd nanoparticles (NPs) catalysts with different nitrogen doping contents (Pd/HCAFR-X, X=0.3, 0.6, 0.9) were prepared for the selective HDO of bio-models compound under mild conditions. Notably, the Pd/HCAFR-0.6 catalyst exhibited excellent catalytic performance for the acetophenone (APh) HDO in polymethylhydrosiloxane (PMHS) at 50 °C for 3 h, and the yield of ethylbenzene was close to 99%. The good catalytic results can be mainly attributed to the unique hollow carbon nanospheres with abundant defects provided by appropriate nitrogen doping content. The large surface area and hierarchical porous structure of the hollow carbon framework offered more active sites, which promoted the transportation of species on the catalyst. In addition, the nitrogen doping amount can adjust the defect degree of the hollow carbon nanospheres, stabilize the dispersion and anchoring of Pd NPs, and then induce the transfer of local electrons. Furthermore, the Pd/HCAFR-0.6 catalyst showed good catalytic performance for bio-models compound HDO after 5 cycles.

Optimization of Catalytic Bromination of Acetophenones Using Taguchi's Method

AbstractA new, efficient and environmental benign one‐pot protocol for the synthesis of α‐bromoacetophenones has been designed via the regioselective monobromination of aromatic carbonyl compounds with Bromodimethylsulfonium Bromide (BDMS) in catalytic environment of MgO nanoparticles and products were obtained in moderate to superior yields. Structure of synthesized compounds were elucidated by their 1H and 13C NMR spectroscopy, further Taguchi based optimization is utilized to maximize the product yield using L27 Orthogonal Array (OA) constructed by five control factors including acetophenones (AP), BDMS, Temperature, Time and MgO with their three levels. The optimal level of AP, BDMS, Temperature, Time and MgO are found up to 1.0 mmol, 2.0 mmol, 60 °C, 50 Min and 10 mol%, respectively.

Green and continuous aerobic oxidation of ethylbenzene over homogeneous and heterogeneous NHPI in a micro-packed bed reactor

Aerobic oxidation of ethylbenzene (EB) has emerged as a promising strategy for the selective synthesis of acetophenone (AP) in line with green chemistry. The integration of flow chemistry into the pharmaceutical industry has been facilitated by recent advancements in microreactor technology. In this work, a continuous micro-packed bed reactor platform is developed to determine the kinetics of aerobic EB oxidation in the presence of N-hydroxyphthalimide (NHPI). The microreactor system offers enhanced gas–liquid mass transfer, leading to a 2-order-of-magnitude increase in the space–time yield of EB oxidation compared to traditional batch reactors. Furthermore, the organic catalyst NHPI is covalently anchored on commercial activated carbon through an imidization reaction. The synthetic heterogeneous catalysts exhibit excellent performance in terms of AP yield of 87.4 % and TOF value of 2.21 h−1 for continuous aerobic EB oxidation.

PdPtVOx/CeO2−ZrO2: Highly efficient catalysts with good sulfur dioxide-poisoning reversibility for the oxidative removal of ethylbenzene

The PdPtVOx/CeO2−ZrO2 (PdPtVOx/CZO) catalysts were obtained by using different approaches, and their physical and chemical properties were determined by various techniques. Catalytic activities of these materials in the presence of H2O or SO2 were evaluated for the oxidation of ethylbenzene (EB). The PdPtVOx/CZO sample exhibited high catalytic activity, good hydrothermal stability, and reversible sulfur dioxide-poisoning performance, over which the specific reaction rate at 160°C, turnover frequency at 160°C (TOFPd or Pt), and apparent activation energy were 72.6 mmol/(gPt⋅sec) or 124.2 mmol/(gPd⋅sec), 14.2 sec−1 (TOFPt) or 13.1 sec−1 (TOFPd), and 58 kJ/mol, respectively. The large EB adsorption capacity, good reducibility, and strong acidity contributed to the good catalytic performance of PdPtVOx/CZO. Catalytic activity of PdPtVOx/CZO decreased when 50 ppm SO2 or (1.0 vol.% H2O + 50 ppm SO2) was added to the feedstock, but was gradually restored to its initial level after the SO2 was cut off. The good reversible sulfur dioxide-resistant performance of PdPtVOx/CZO was associated with the facts: (i) the introduction of SO2 leads to an increase in surface acidity; (ii) V can adsorb and activate SO2, thus accelerating formation of the SOx2− (x = 3 or 4) species at the V and CZO sites, weakening the adsorption of sulfur species at the PdPt active sites, and hence protecting the PdPt active sites to be not poisoned by SO2. EB oxidation over PdPtVOx/CZO might take place via the route of EB → styrene → phenyl methyl ketone → benzaldehyde → benzoic acid → maleic anhydride → CO2 and H2O.

Design of frontal chromatography separation of 1-phenylethanol and acetophenone using a hydrophobic resin

Adsorption and chromatographic processes havegood potential in the purification of natural aromas produced via biocatalytic routes. This work deals with the recovery of 1-phenylethanol (PE) from mixtures containing different amounts of acetophenone (AP). Amberlite FPX68, an industrial adsorbent with high selectivity with respect to acetophenone, was chosen for the separation of PE and AP by frontal chromatography. Small-scale experiments were performed for two different feed compositions and various flow rates and bed lengths. Using the target purity of 99 %, promising yields close to 90 % were obtained. The breakthrough curves were fitted with the equilibrium dispersive model, which provided HETP values under the different conditions. The obtained dependences of HETP on flow velocity complied with the Van Deemter equation. The contributions of individual phenomena responsible for adsorption zone broadening were analyzed. The experimental and modelling results obtained for the small-scale column became the basis for the scale-up of frontal chromatography separation of PE with an annual capacity up to 500 kg.

Effective photodegradation of antibiotics by guest-host synergy between photosensitizer and bismuth vanadate: Underlying mechanism and toxicity assessment

The removal of antibiotics in wastewater has attracted increasing attention. Herein, a superior photosensitized photocatalytic system was developed with acetophenone (ACP) as the guest photosensitizer, bismuth vanadate (BiVO4) as the host catalyst and poly dimethyl diallyl ammonium chloride (PDDA) as the bridging complex, and used for the removal of sulfamerazine (SMR), sulfadiazine (SDZ) and sulfamethazine (SMZ) in water under simulated visible light (λ > 420 nm). The obtained ACP-PDDA-BiVO4 nanoplates attained a removal efficiency of 88.9%–98.2% for SMR, SDZ and SMZ after 60 min reaction and achieved kinetic rate constant approximately 10, 4.7 and 13 times of BiVO4, PDDA-BiVO4 and ACP-BiVO4, respectively, for SMZ degradation. In the guest-host photocatalytic system, ACP photosensitizer was found to have a great superiority in enhancing the light absorption, promoting the surface charge separation-transfer and efficient generation of holes (h+) and superoxide radical (·O2−), greatly contributing to the photoactivity. The SMZ degradation pathways were proposed based on the identified degradation intermediates, involving three main pathways of rearrangement, desulfonation and oxidation. The toxicity of intermediates was evaluated and the results demonstrated that the overall toxicity was reduced compared with parent SMZ. This catalyst maintained 92% photocatalytic oxidation performance after five cyclic experiments and displayed a co-photodegradation ability to others antibiotics (e.g., roxithromycin, ciprofloxacin et al.) in effluent water. Therefore, this work provides a facile photosensitized strategy for developing guest-host photocatalysts, which enabling the simultaneous antibiotics removal and effectively reduce the ecological risks in wastewater.

Elucidating mechanism of ethylbenzene oxidation catalyzed by carbon‐based catalysts with kinetic modeling

AbstractEthylbenzene (EB) oxidation to oxygenated products catalyzed by carbon nanotubes (CNTs) and CNTs with confined cobalt nanoparticles (Co@C/CNTs) are conducted. Co@C/CNTs with enhanced interfacial charge transfer displays a unique activity. A kinetic model with the simplified network is established, in which seven elementary reactions with prominent features of EB oxidation are selected. The main parameters, reaction rate constant (k) and active energy (Ea) are obtained. Co@C/CNTs could speed up most elementary steps and reduce energy barriers, thus improving the overall activity. The homolytic cleavage of peroxide is confirmed to be the rate‐determining step (RDS). The k ratio (1.55) of acetophenone (AcPO)/1‐phenylethyl alcohol (PEA) is found to be close to the experimental result (rAcPO/rPEA, 1.30). The prediction of EB oxidation is simulated, showing that the synthesis of AcPO dominates the reaction route, while the addition of PEA would prohibit the reaction.

SCILL-SILP hybrid catalytic system by employing carbon nanotubes as a support for the selective oxidation of ethylbenzene to acetophenone

Hydrocarbon oxidation to more valuable products is one of the most crucial industrial petrochemical processes. To improve efficiency, economic effectiveness, and reduction of waste production by conventional processes, the development of active and selective catalysts is still an important area of research. To cope with these challenges, we developed a catalytic system that utilized molecular oxygen to oxidize ethylbenzene (EB) to acetophenone (AcPO). The catalyst was prepared by coating a thin layer of a mixture of selected ionic liquid 1-ethyl-3-methylimidazolium octylsulfate and N-hydroxyphthalimide over industrial-grade multiwalled carbon nanotubes functionalized with copper(II) ions. This unique catalyst represented a hybrid catalytic system via the combination of solid catalyst with an ionic liquid layer (SCILL) and a supported ionic liquid phase (SILP) system. The oxidation reactions were performed at 80 °C and 0.1 MPa for 6 h. SCILL-SILP hybrid catalytic system exhibited exceptional performance with ∼27 % EB conversion and ∼77 % AcPO selectivity. The recyclability and reusability of the prepared catalysts were also investigated. The copper content was determined using inductively coupled plasma mass spectrometry (ICP-MS). Scanning electron microscopy (SEM) and transmission electron microscopy(TEM)were used to study the morphologies of the catalysts. Energy dispersive spectroscopy (EDS) was used to detect the immobilized copper on the functionalized CNTs while N2 physisorption analysis was employed to study the textural properties of the catalysts. Fourier-transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA) were used to study the freshly synthesized and recycled catalysts.

Reversing adsorption and separation of 1-phenylethanol and acetophenone in organic phase via β-ketoenamine-linked covalent organic frameworks

Adsorption is considered as a promising method to purify the mixed acetophenone (AP) and 1-phenylethanol (1-PE) that are generally difficult to separate. Many efforts have been made to improve the preferential uptake of AP over 1-PE in aqueous phase, but there exists a practical bottleneck associated with their limited aqueous solubility. Herein, we demonstrate unprecedented reversal of selectivity in the organic medium enabled by β-ketoenamine-linked covalent organic frameworks (COFs), which were fabricated successfully by polycondensation between 1,3,5-triformylphloroglucinol (Tp) and diamines. The dependence of selective adsorption ability toward 1-PE on pore size was firstly investigated experimentally, indicating that TpBZ-COF with moderate pore size outperformed other analogues. The adsorption behaviors of 1-PE and AP onto TpBZ-COF were examined systematically. The evaluation results revealed a strong affinity toward 1-PE versus AP as well as excellent stability in recycling experiments. Further, the dynamic breakthrough experiments confirmed the practical application potential and remarkable recyclability. To probe the mechanism and structure–activity relationship, an imine-linked COF possessing similar porous structure was used as a reference for comparison of separation performance both experimentally and theoretically. The occurrence of hydrogen bonding between the hydroxyl of 1-PE and β-ketoenamine-linkage as H-bond acceptor in suitable pore spaces endows TpBZ-COF a fantastic candidate for purifying 1-PE and AP from petrochemical by-products.

Preparation and Electrocatalytic Application of Copper- and Cobalt-Carbon Composites Based on Pyrolyzed Polymer

Copper- and cobalt-containing carbon composites were prepared by pyrolysis of an aniline-formaldehyde polymer (AFP) doped with the metal oxides, followed by the reduction of metal cations in an electrochemical cell. AFP + metal oxide nanocomposites were synthesized by introducing a metal salt during the polycondensation of aniline with formaldehyde and by alkaline precipitation of metal oxides into the polymer matrix. The heat treatment was carried out at 400, 500 and 700 °C. Microscopic studies revealed the formation of CuO crystallites in the shape of "stars" on the heat-treated carbon material. The resulting composites were saturated with hydrogen in an electrochemical system, which was accompanied by the reduction of copper and cobalt cations, and the appearance of the metals in zero-valence state. The so-prepared Cu + copper oxides/C and Co + Co(OH)2/C composites were used as electrocatalysts in the electrohydrogenation of acetophenone (APh). Compared to the electrochemical reduction of APh on a copper cathode (without catalysts), an increase in the rate of this process (by 2–4 times) in the presence of the composites and an increase in the APh conversion with the selective formation of 1-phenylethanol were established.