Results 131 to 140 of about 129,275 (339)

Selectivity Beyond Mass: Real-Time Isomer Separation Using SLIM IMS Coupled to PTR-MS. [PDF]

open access: yesJ Mass Spectrom
ABSTRACT Proton‐transfer‐reaction—mass spectrometry (PTR‐MS) provides real‐time analysis of volatile organic compounds (VOCs) relevant to atmospheric research, food and flavor characterization, industrial process control, and medical applications. However, PTR‐MS is inherently limited in its ability to resolve isomers of molecules with the same mass‐to‐
Jordan J   +6 more
europepmc   +2 more sources

Sensitivity Enhancement of Benzene Sensor Using Ethyl Cellulose-Coated Surface-Functionalized Carbon Nanotubes [PDF]

open access: hybrid, 2018
Thanattha Chobsilp   +7 more
openalex   +1 more source

Metal‐Free Covalent Organic Frameworks for Photocatalytic CO2 Reduction

open access: yesChemistryEurope, EarlyView.
This review presents an environmentally sustainable strategy to address the critical issue of escalating atmospheric CO2 levels. It explores the application of metal‐free covalent organic frameworks in a photocatalytic approach, offering a green and efficient strategy for carbon dioxide reduction and contributing to climate change mitigation.
Supriti Dutta   +3 more
wiley   +1 more source

Ring‐opening metathesis polymerization‐Derived Organoborane Polymers as Strong Lewis Acids and Luminescent Materials

open access: yesChemistryEurope, EarlyView.
Ring‐opening metathesis polymerization offers access to borane polymers with tunable Lewis acidity, environmental stability, and luminescence. The Lewis acid strength approaches that of B(C6F5)3 when R = Cl and Ar = C6F5, high stability is ensured with chlorophenyl or naphthyl pendent groups (Ar = ClPh, Np), and strong emission is achieved with a ...
James McQuade   +5 more
wiley   +1 more source

One‐Pot Ruthenium‐Catalyzed Synthesis of Benzyl/Allyl‐Halide Substituted (dihydro)naphthalenes via Radical Benzannulation

open access: yesChemistryEurope, EarlyView.
A one‐pot protocol to synthesize reactive benzyl‐ and allyl‐halide‐substituted (dihydro)naphthalenes from 2,3‐aryl‐1,3‐butadiene substrates and halogenated alkanes has been developed, using [Cp*RuCl(PPh3)2] as the catalyst. Mechanistic studies revealed an atom transfer radical addition and radical benzannulation sequence, followed by HCl elimination ...
Nicole S. van Leeuwen   +9 more
wiley   +1 more source

Skeletal Editing from Pyridine to Aniline via C‐Insertion and N‐Isomerization

open access: yesChemistryEurope, EarlyView.
A concise protocol is presented that converts pyridines into anilines by externalizing the original pyridine nitrogen at either the "ipso" or "ortho" position, which results in para or meta‐primary aniline products. A key carbene‐insertion step precedes nitrogen migration, preserving both ring size and overall structure.
Yun Luo   +3 more
wiley   +1 more source

The Techniques of Thin Layer Chromatography and the Study of Carbohydrates Using Thin Layer Chromatography [PDF]

open access: yes, 1977
Refined Kraft pulp is found to contain D (+), Mannose, D (+) Xylose, and Glucose; and not to contain Galactose. Silia gel plates and Kieselguhr plates were used for the separation.
Hippchen, Dennis J.
core   +1 more source

Defect Suppression via Tailoring Functionalized Additives for Efficient and Stable CsPbI3 Perovskite Solar Cells

open access: yesCarbon Energy, EarlyView.
This study proposed a structure‐designed benzohydrazide derivative, namely 4‐methoxybenzohydrazide (MeOBH), as an additive to regulate crystallization, passivate defects, optimize energy‐level structure, and enhance phase stability of β‐CsPbI3 perovskite films.
Haiyan Zhao   +10 more
wiley   +1 more source

Shedding Light on Synthetic Autocatalysis: From Conventional Closed‐Shell Chemistries to Overlooked Open‐Shell Occurrences

open access: yesChemistry – A European Journal, EarlyView.
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley   +1 more source

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