Chemical Precursors Research Articles

Synthesis, Characterization, and Thermal Properties of Liquid Iron Amidinates and Their Potential as Chemical Vapor Deposition Precursors for Producing Iron-Containing Films

Synthesis, Characterization, and Thermal Properties of Liquid Iron Amidinates and Their Potential as Chemical Vapor Deposition Precursors for Producing Iron-Containing Films

Macrocyclic porphyrin photocatalysts without metal chelation: A novel pathway for complete degradation of tough halophenols with longwave visible LED light source

Halophenols are toxic and persistent pollutants in water environments which poses harm to various organisms. Due to their high stability and long residence time, ultraviolet radiation, heavy metals and oxidizing agents have been largely adopted on treating these compounds. However, these treatment methods could pose toxicity or hazardous risks to the marine environment and plant operators. In this study, a water-soluble porphyrin photocatalyst was synthesized and introduced for halophenol treatment using UV-free LED white light. The porphyrin catalyst is a macrocyclic ring consisting of pyrroles linked with methine bridges, the highly conjugated ring provided the superior functionality of visible light absorption. Surprisingly, over 99 % degradation of halophenols and over 90 % dehalogenation have been achieved without metal chelation, even higher than those of transition metal porphyrins with inclusion of Fe3+, Zn2+, Cu2+, Co2+, Ni2+, and Mn2+. Ring-opening reactions were confirmed with the formation of carboxylic acids; dicarboxylic acids like acrylic acid, and malonic acid; while fumaric acid was the main product. Total organic carbon results indicated no CO2 produced during the reaction. Triplet absorbance and scavenger studies also indicated that singlet oxygen and conduction band electrons are the main radical species for halophenol degradation. The 100-fold singlet emission quenching over triplet absorption quenching indicated that the excited electrons tend to be transferred via singlet state. This concept brings along new approaches detoxifying halophenol-related wastewater without UV, metals and other additives, which is more environmentally-friendly and sheds light to the conversion of toxic materials into useful chemical precursors.

Asparagus officinalis Herb-Derived Carbon Quantum Dots: Luminescent Probe for Medical Diagnostics.

The utilization of natural materials for the synthesis of highly fluorescent carbon quantum dots (CQDs) presents a sustainable approach to overcome the challenges associated with traditional chemical precursors. Here, we report the synthesis of novel S,N-self-doped CQDs (S,N@CQDs) derived from asparagus officinalis herb. These S,N@CQDs exhibit 16.7 % fluorescence quantum yield, demonstrating their potential in medical diagnostics. We demonstrate the efficacy of S,N@CQDs as luminescent probes for the detection of anti-pathogenic medications metronidazole (MTZ) and nitazoxanide (NTZ) over concentration ranges of 0.0-180.0 μM (with a limit of detection (LOD) of 0.064 μM) and 0.25-40.0 μM (LOD of 0.05 μM), respectively. The probes were successfully applied to determine MTZ and NTZ in medicinal samples, real samples, and spiked human plasma, with excellent recovery rates ranging from 99.82 % to 103.03 %. Additionally, S,N@CQDs demonstrate exceptional efficacy as diagnostic luminescent probes for hemoglobin (Hb) detection over a concentration range of 0-900 nM, with a minimal detectability of 9.24 nM, comparable to commercially available medical laboratory diagnostic tests. The eco-friendly synthesis and precise detection limits of S,N@CQDs meet necessary analytical requirements and hold promise for advancing diagnostic capabilities in clinical settings. This research signifies a significant step towards sustainable and efficient fluorescence-based medical diagnostics.

Compounds with Chelating 3-Dimethylamino-1-propyl Ligands as Chemical Vapor Deposition Precursors. Synthesis and Characterization of M[(CH2)3NMe2]2 Complexes of Nickel(II), Palladium(II), and Platinum(II)

Compounds with Chelating 3-Dimethylamino-1-propyl Ligands as Chemical Vapor Deposition Precursors. Synthesis and Characterization of M[(CH₂)₃NMe₂]₂ Complexes of Nickel(II), Palladium(II), and Platinum(II)

Femtosecond laser-enabled facile tuning of Cu selectivity towards long-chain products in CO2 electroreduction

In the quest to mitigate excessive CO2 emissions, the electrochemical reduction of CO2 (eCO2R) into multi-carbon fuels and vital chemical precursors emerges as a compelling strategy. Meticulous control of the C–C coupling on a catalyst surface is a grand challenge in the selective production of desired C2+ products. Ethane and propanol are among the most desirable C2+ products in the gas and liquid phase, respectively. Herein, we demonstrate facile femtosecond laser-enabled tuning of Cu selectivity towards ethane and propanol. The laser-enabled tailoring of the Cu surface induces a shift from C1 products to ethane and propanol. This shift in product composition is attributed to the concurrent creation of hierarchical porous structures, the stabilization of {111}, {200}, and {220} Cu2O facets, and the promotion of the Cu1+ oxidation state. These alterations collectively enhance the adsorption strength, leading to an increased propensity for C-C coupling and, consequently, an elevated selectivity toward C2+ products.

First detection of CF+ in the Large Magellanic Cloud

Context. CF+ has been established as a valuable diagnostic tool for investigating photodissociation regions (PDRs) and fluorine abundances in the Milky Way. However, its role in extragalactic environments remains largely uncharted. Aims. Our objective is to explore the significance of CF+ in the Large Magellanic Cloud (LMC) and assess its utility as a probe for examining C+ and fluorine abundances in external galaxies. Methods. We performed pointed CF+ observations toward an active star-forming region, N113 in the LMC, using the Atacama Pathfinder EXperiment 12 m submillimeter telescope. Results. We report the first discovery of CF+ in the LMC through the successful detection of the CF+ (2→1) and (3→2) lines. The excitation models indicate that CF+ emission originates from dense PDRs characterized by an H2 number density of (0.5–7.9) × 104 cm−3 in N113. Our observations provide the first constraint on the fluorine abundance in molecular clouds in the LMC, ≲1.7 × 10−9. This value is about an order of magnitude lower than those previously measured toward red giants in the LMC, indicative of fluorine deficiency in the molecular gas. The estimated column density ratio between C+ and CF+ appears to be lower than the anticipated equilibrium ratio derived from the fluorine abundance in red giants. Both phenomena can be explained by the deficiency of CF+ caused by the freeze-out of its primary chemical precursor, HF, onto dust grains. Conclusions. The deficiency of CF+ within molecular clouds suggests that the measurements presented in this work serve exclusively as conservative estimates, establishing lower bounds for both the fluorine abundance and C+ column densities in external galaxies.

Promoter dependent RNA polymerase II bypass of the epimerizable DNA lesion, Fapy•dG and 8-Oxo-2'-deoxyguanosine.

Formamidopyrimidine (Fapy•dG) is a major lesion arising from oxidation of dG that is produced from a common chemical precursor of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-OxodGuo). In human cells, replication of single-stranded shuttle vectors containing Fapy•dG is more mutagenic than 8-OxodGuo. Here, we present the first data regarding promoter dependent RNA polymerase II bypass of Fapy•dG. 8-OxodGuo bypass was examined side-by-side. Experiments were carried out using double-stranded shuttle vectors in HeLa cell nuclear lysates and in HEK 293T cells. The lesions do not significantly block transcriptional bypass efficiency. Less than 2% adenosine incorporation occurred in cells when the lesions were base paired with dC. Inhibiting base excision repair in HEK 293T cells significantly increased adenosine incorporation, particularly from Fapy•dG:dC bypass which yielded ∼25% adenosine incorporation. No effect was detected upon transcriptional bypass of either lesion in nucleotide excision repair deficient cells. Transcriptional mutagenesis was significantly higher when shuttle vectors containing dA opposite one of the lesions were employed. For Fapy•dG:dA bypass, adenosine incorporation was greater than 85%; whereas 8-OxodGuo:dA yielded >20% point mutations. The combination of more frequent replication mistakes and greater error-prone Pol II bypass suggest that Fapy•dG is more mutagenic than 8-OxodGuo.

One-step microwave-assisted synthesis of fluorescent carbon quantum dots for determination of ascorbic acid and riboflavin in vitamin supplements

The synthesis of carbon quantum dots (CQDs) using chemical precursors with different organic groups is a strategy to improve optical properties and expand applications in several fields of research such as Analytical Chemistry. Ascorbic acid and riboflavin are widely used in human food supplementation, making quality monitoring of these vitamin supplements relevant and necessary. In this work, disodium ethylenediaminetetraacetic, sodium thiosulfate and urea were applied to obtain CQDs through a single-step microwave-assisted synthesis. The CQDs were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, X-ray powder diffraction, infrared spectroscopy, zeta potential measurements, ultraviolet–visible spectroscopy and photoluminescence spectroscopy. The synthesized nanoparticles exhibited satisfactory and stable optical properties with luminescence at 430 nm, water solubility, and fluorescence quantum yield of 8.9 %. They were applied in the quantification of ascorbic acid and riboflavin in vitamin supplements. The fluorescence mechanisms observed were dynamic quenching for the CQDs/Cr(VI) sensor, followed by a return of fluorescence in the presence of ascorbic acid, and static quenching and inner filter effect in the interaction with riboflavin. Factorial designs 23 and 24 were used to optimize the analytical parameters. The CQDs/Cr(VI) sensor used in the determination of ascorbic acid, employing an on–off-on strategy, resulted in a linear range of 0.5 to 50 µg mL−1 and a limit of detection of 0.15 µg mL−1. The ratiometric fluorescence used in the determination of riboflavin resulted in a linear range of 0.1 to 7 µg mL−1 and a limit of detection of 0.09 µg mL−1. The analytical results for ascorbic acid were compared to the reference method of the Brazilian pharmacopeia, showing accuracy and precision according to the Brazilian Health Regulation Agency. Therefore, the synthesized CQDs were used to determine ascorbic acid and riboflavin in vitamin supplements, and the application of this nanomaterial can be expanded to different analytes and matrices, using simple and low-cost analysis techniques.

Earthquake prediction using satellite data: Advances and ahead challenges

Due to the considerable loss of life and damages caused by powerful Earthquakes, along with the strengthening of structures and disaster management systems, many researches are being conducted associated with the possibility of creating Earthquake warning systems. However, no reliable scientific report on successful Earthquake prediction has been published so far. Although there are a couple of published scientific papers indicating the detection of unusual changes in physical and chemical parameters obtained from ground stations, but due to the limitations of in-situ measurement in terms of number, location, time and cost, there was no noticeable progress in Earthquake warning. After the advent of remote sensing satellites, the number of statistical studies related to Earthquake precursors increased significantly, and most of them emphasized the existence of abnormal behaviors in physical and chemical precursors around the time (about 1–30 days before) and locations of powerful Earthquakes. In this study, an attempt has been made to address the advances and challenges in the way of Earthquake prediction using satellite data and provide a perspective of the future of these researches. It should be noted that the increase in the number of satellites designed and launched specially for Earthquake studies, the variety of available Earthquake precursors (multi-precursor analysis), the development of classic and intelligent anomaly detection and predictor algorithms (multi-method analysis), the provision of intelligent systems for the integration of various precursors (fusion and decision systems), the creation of cloud storing and processing data services (Google Earth Engine, Giovanni, etc.) and the development of intelligent user interfaces for public, have made researchers more hopeful for the appearance of low-uncertainty Earthquake warning systems in the near future.

Electrochemical characteristics of flexible open-cell supercapacitors employing different electrolyte types: KOH and ionic liquid

A carbonate hydroxide compound with substantial wettability was deposited on a porous Ni foam substrate, employing the Ni-based chemical precursor by a facile hydrothermal method. The resulting Ni2(CO3)(OH)2 electrode exhibits a nanowire structure characterized by a significant surface area. These electrodes represent highly promising materials for faradaic capacitors. They demonstrate high wettability on the electrode surface, facilitating charge and discharge processes on the electrode surface through redox reactions. A flexible hybrid open-cell supercapacitor, designed to operate at 1.5 V, was constructed with the Ni2(CO3)(OH)2 electrode as the positive terminal and graphene as the negative terminal, employing two distinct electrolytes (KOH and ionic liquid named MPPyFSI with 1-Methyl-1-propylpyrrolidinium Bis(fluorosulfonyl)imide structure). The open-cell devices, fabricated with 6 M KOH and MPPyFSI electrolyte, exhibit high energy densities of 39.6 and 24.8 Wh kg−1 and power densities of 1752.1 and 2908.5 W kg−1 at current densities of 2 A g−1, respectively. Furthermore, the energy storage devices utilizing aqueous KOH and MPPyFSI demonstrate excellent stability, maintaining 73.4 and 87.1% of their specific capacity after 5,000 charge/discharge cycles. The mechanical properties of the flexible open-cell device were characterized, and the electrochemical values corresponding to the banding angle of the device were measured.

An in vitro evaluation of partial energy replacement in a total mixed ration with volatile fatty acids derived from agro-industrial residues

AbstractThe scientific interest in volatile fatty acids (VFAs) as an energy source and chemical precursor in ruminant diets has been longstanding, as it has significant implications for animal physiology and well-being. The present study explores the substitution of volatile fatty acids (VFAs) derived from agro-food residues via acidogenic fermentation as an alternative energy source in ruminant feed. Utilizing the gas production method, rumen digestibility assays were conducted, wherein the recovered VFA effluent from the acidogenic fermentation of apple pomace and potato protein liquor was substituted for 10%, 20%, and 30% of the total mixed ration (TMR) energy. Various parameters such as gas, VFA yield and composition, VFA peak intervals, changes in pH, and ammonium nitrogen content were investigated. Based on the results obtained, provision of 20% and 30% of the energy with VFAs did not increase methane production or did not cause significant pH alternations. Nevertheless, such supplementation resulted in increased production and accumulation of VFAs in the rumen media. The bioconversion of agro-food side streams into VFAs opens a new path in sustainable nutrient recovery and feed production from low value agro-industrial residues. Graphical Abstract

Novel Hybrid Ferromagnetic Fe–Co/Nanodiamond Nanostructures: Influence of Carbon on Their Structural and Magnetic Properties

This study introduces a novel magnetic nanohybrid material consisting of ferromagnetic (FM) bcc Fe–Co nanoparticles (NPs) grown on nanodiamond (ND) nanotemplates. A combination of wet chemistry, which produces chemical precursors and their subsequent thermal treatment under vacuum, was utilized for its development. The characterization and study of the prepared samples performed with a range of specialized experimental techniques reveal that thermal treatment of the as-prepared hybrid precursors under a range of annealing conditions leads to the development of Co-rich Fe–Co alloy NPs, with average sizes in the range of 6–10 nm, that exhibit uniform distribution on the surfaces of the ND nanotemplates and demonstrate FM behavior throughout a temperature range from 2 K to 400 K, with maximum magnetization values ranging between 18.9 and 21.1 emu/g and coercivities ranging between 112 and 881 Oe. Moreover, 57Fe Mössbauer spectroscopy reveals that apart from the predominant bcc FM Fe–Co phase, iron atoms also participate in the formation of a secondary martensitic-type Fe–Co phase. The emergence of this distinctive phase is attributed to the diffusion of carbon atoms within the Fe–Co lattices during their formation at elevated temperatures. The source of these carbon atoms is related to the unique morphological properties of the ND growth matrices, which facilitate surface sp2 formations. Apart from their diffusion within the Fe–Co NP lattice, the carbon atoms also reconstruct layered graphitic-type nanostructures enveloping the metallic alloy NPs. These non-typical nanohybrid materials, reported here for the first time in the literature, hold significant potential for use in applications related, but not limited to, biomedicine, biopharmaceutics, catalysis, and other various contemporary technological fields.

(E)-1-(5-(Hydroxymethyl) furan-2-yl)-4,4-dimethylpent-1-en-3-one

This study presents a novel approach in the realm of catalytic organic synthesis by integrating biomass catalytic conversion with organic synthesis techniques. Utilizing N-acetylglucosamine as the primary feedstock, the first phase of the research involves its catalytic transformation into 5-hydroxymethylfurfural (HMF). The subsequent phase employs a condensation reaction between HMF and 3,3-Dimethyl-2-butanone to synthesize a new compound, (E)-1-(5-(hydroxymethyl) furan-2-yl)-4,4-dimethylpent-1-en-3-one. This two-step process not only demonstrates the feasibility of converting biomass into valuable chemical precursors but also exemplifies the synthesis of novel compounds through green chemistry principles. The successful execution of this methodology offers fresh insights and opens new avenues for advancements in catalytic organic synthesis, emphasizing sustainability and efficiency.

Arginine Acts as both Co-Solvent and Catalyst in Regioselective Eutectic-Mediated Dimerization of Levulinic Acid.

A simple, solvent-free arginine-catalyzed aldol dimerization of levulinic acid was achieved via the simultaneous formation of a eutectic mixture. Dimers of levulinic acid are valued as biomass-derived fine chemical precursors, with potential to upgrade to bio-jet fuels or N-containing functional chemicals. Typically, these dimers are produced as isomeric mixtures using high temperatures and a variety of solid inorganic catalysts or mineral acids. In this study, an organocatalytic and regioselective dimerization was achieved at 22 % conversion on either a bench or kilogram scale using mild temperatures and only L-arginine as both a co-solvent and catalyst. The intricate H-bonding network comprising the eutectic solvent was harnessed to produce only one product, minimizing side reactivity and preserving the reactants for recycling.

Physical Methods as Pretreatment of Prickly Pear and Pineapple Peels for Producing Enzymes and Chemical Precursors

Physical Methods as Pretreatment of Prickly Pear and Pineapple Peels for Producing Enzymes and Chemical Precursors

Differentiation of regioisomeric N-substituted meta-chlorophenylpiperazine derivatives

A series ofN,N-disubstituted piperazines were synthesized containing the structural elements of meta-chlorophenylpiperazine (mCPP) in combination with methoxybenzyl-, and dimethoxybenzyl substituents to yield nineN,N-disubstituted piperazine compounds. These nine potential designer-like drug analogs were prepared based on common designer trends and regioisomeric differentiation was based on gas chromatography-mass spectrometry (GC–MS) and gas chromatography-vapor phase infrared (GC–vpIR) studies.The compounds in this study have not been reported as drugs of abuse at this time. However, commercial availability of precursor chemicals including mCPP suggests the possibility of further designer exploration. Capillary GC separation showed the regioisomers to elute according to the position of aromatic ring substitution and/or the degree of substituent crowding on the aromatic ring. Numerous electron ionization (EI) mass spectral fragment ions occur via processes initiated by one of the two nitrogen atoms of the piperazine ring. The major EI-MS fragment ions observed in all nine spectra occur at m/z 195 from the loss of the substituted benzyl radical and the cation atm/z56 (C3H6N)+from the piperazine ring. Unique radical cations at m/z 136 and m/z 152 are characteristic of the 2,3- and 3,5-dimethoxybenzyl isomers, respectively. The vapor phase infrared spectra for all nine compounds show a strong absorption band in the 1591–1593 cm−1region indicative of the chloroaniline moiety. Numerous bands in the 1600–650 cm−1region provide data for the differentiation of the methoxy and dimethoxybenzyl ring substitution patterns. Thus, a combination of EI-MS and vapor phase IR allow for the differentiation and specific identification of each regioisomer in this study.

Catalytic co-pyrolysis of cabbage waste and plastics with Ni/ZSM-5 catalysis to produce aromatic-rich oil

This study investigates the selective production of aromatics through the co-pyrolysis of cabbage waste and plastics followed by catalytic reforming with Ni-modified ZSM-5. Co-pyrolysis significantly improves the inflection point (a parameter for determining thermal stability) to 251.3 °C from 232.7 °C. This process also enhances the relative yield of olefins and phenols, which are precursors for aromatic production to 25.46 and 17.23 respectively, up from 13.87 to 12.05. Furthermore, catalytic pyrolysis elevates the relative yield of aromatics to 53.4, as confirmed by Thermogravimetric Analysis (TGA) and Thermogravimetric-Fourier Transform Infrared Spectroscopy (TG-FTIR) analyses. GC-MS confirms the enhanced formation of valuable chemical precursors via co-pyrolysis such as phenols and olefines to 18.67 % and 22.13 % leading to a 63.81 % selective yield of aromatics in the final oil with 10Ni/ZSM-5. Ni modification of ZSM-5 is influential in decreasing PAH formation (7.26 % from 20.37 %), indicating that this two-step process is an effective method for transforming waste into high-quality bio-oil with enriched aromatic content.

Comparative Ablation Behaviors of 2D Needled C/SiC and C/SiC-ZrC Composites

To investigate the effect of ZrC on the ablative properties of C/SiC composites in a high-temperature environment, the oxidative ablation of C/SiC and C/SiC-ZrC composites at high-temperatures was examined through ablation tests. In this study, two ceramic matrix composites, C/SiC and C/SiC-ZrC, were prepared by chemical vapor deposition and precursor impregnation pyrolysis. The ablation properties of the materials were tested and analyzed using an oxyacetylene flame to simulate a high-temperature environment. The results revealed that the line ablation rate of C/SiC-ZrC was 8.48% and 20.81% lower than that of C/SiC at 30 s and 60 s, respectively. At the same ablation time, the depth of the crater resulting from erosion of the C/SiC material by the high-temperature airflow was deeper than that of C/SiC-ZrC. The traces of the fibers subjected to erosion were more prominent. In a longitudinal comparison, the mass ablation rate of C/SiC-ZrC material decreased with the increase in time, while the line ablation rate initially increased rapidly and then decreased. From 30 s to 90 s of ablation, the line ablation rate and mass ablation rate decreased by 55.62% and 89.5%, respectively. The overall trend for both rates was a decrease with the increase in time. Under the same ablation time, the ablation rate of C/SiC-ZrC was generally lower than that of C/SiC. This is because the generated molten ZrO2 was more viscous and denser than SiO2, effectively blocking oxidizing gases from penetrating the interior of the material. The molten ZrO2 provided better protection for the substrate in the high-temperature environment.

The Latest Studies for the Manufacture of Nanoparticles in Iraq during the Last Ten Years Ago

Silver nanoparticles (AgNPs) have gained immense consideration recently as a result of their exceptional properties and diverse interference in a variety of fields. The AgNPs synthesis involves various and biological, chemical, and physical methods, each offering distinct compensations in terms of size control, stability, and reproducibility. Physical methods, such as irradiation, result in monodisperse nanoparticles with excellent control over size and shape. Chemical techniques, like reduction with reducing agents or chemical precursors, offer scalability and control over nanoparticle size. Moreover, green synthesis methods employing plant extracts, fungi, and bacteria have emerged as eco-friendly alternatives, reducing the reliance on hazardous chemicals. Characterization of AgNPs is necessary to understand their characteristics and potential applications fully. Techniques such as X-ray diffraction (XRD), UV-Vis spectroscopy, light scattering (DLS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM), dynamic are commonly used to identified anf characterized the nanoparticles. The applications of AgNPs span across several sectors. In the biomedical field, AgNPs exhibit potent antimicrobial properties against a broad spectrum of pathogens, making them promising candidates for wound dressings, antibacterial coatings, and drug delivery systems. Additionally, their use in cancer therapy has shown potential for targeted drug delivery and localized hyperthermia treatment. However, despite their numerous applications, challenges remain in terms of toxicity and environmental impact. Research efforts are ongoing to address these concerns and develop safer nanomaterials. This review article concludes that silver nanoparticles represent a fascinating class of nanomaterials with immense potential in various fields. Continued research and development in the synthesis, characterization, and application of AgNPs will undoubtedly lead to new and exciting advancements in science and technology.

A comparative pyrolysis study of tetraethoxysilane and tetraethoxymethane: Insight into congener substitution effects on pyrolysis chemistry of siloxane flame synthesis precursors

The pyrolysis of siloxane precursors, such as tetraethoxysilane (TEOS), is commonly employed in the flame synthesis and chemical vapor deposition of silica nanoparticles. In this work, the flow reactor pyrolysis of TEOS is studied using gas chromatography (GC) and synchrotron vacuum ultraviolet photoionization mass spectrometry (SVUV-PIMS), and the congener substitution effects from the central C atom to the central Si atom are investigated through comparison with its hydrocarbon counterpart tetraethoxymethane (TEOM). Pyrolysis models of TEOS and TEOM are constructed and validated against the measured results. Modeling analysis, including rate of production analysis and sensitivity analysis, provides insights into chemistry in fuel consumption and product formation. In contrast, the observations of silicon-containing products in SVUV-PIMS experiments provide evidence for crucial decomposition pathways of TEOS. It is observed that TEOS exhibits significantly higher stability than TEOM under pyrolysis conditions. The most abundant products in the pyrolysis of TEOS and TEOM are ethylene and ethanol, and TEOS produces more hydrocarbon products than TEOM. The lower pyrolysis reactivity of TEOS is attributed to the slower unimolecular decomposition reaction which dominates the decomposition of TEOS than TEOM. This can be explained by the hindrance of the extremely strong Si-O bond resulting from the significantly different electronegativity between Si and O. The higher initial decomposition temperature of TEOS enhances the contribution of other decomposition channels, such as C-C bond dissociation and H-abstraction reactions, in TEOS consumption. This leads to the abundant formation of hydrocarbon productions such as methane, ethane, and acetaldehyde. As the main pyrolysis product, the ethanol produced by TEOM pyrolysis is four times that of TEOS due to the congener substitution effects. The ethanol formation pathway in TEOS pyrolysis is different from that in TEOM pyrolysis, which is mainly formed via a newly proposed multi-step mechanism, resulting in a lower yield in TEOS pyrolysis.