Results 111 to 120 of about 15,945 (209)

Thermometer Ions, Internal Energies, and In‐Source Fragmentation in Ambient Ionization

open access: yesMass Spectrometry Reviews, Volume 45, Issue 2, Page 260-281, March/April 2026.
ABSTRACT Ionization and fragmentation are at the core of mass spectrometry. But they are not necessarily separated in space, as in‐source fragmentation can also occur. Here, we survey the literature published since our 2005 review on the internal energy and fragmentation in electrospray ionization sources.
Emilie Bertrand, Valérie Gabelica
wiley   +1 more source

NMR‐Based Structural Analysis of Highly Substituted Pyridines From Kondrat'eva Aza‐Diels–Alder Cycloadditions

open access: yesMagnetic Resonance in Chemistry, Volume 64, Issue 3, Page 324-332, March 2026.
We report the results from a kinetic and mechanistic investigation of an inverse‐electron‐demand Diels–Alder (IEDDA) cycloaddition involving an oxazole‐type diene synthesized via an Ugi–Zhu multicomponent reaction (UZ‐3CR). ABSTRACT Pyridines are a crucial class of heterocycles with widespread applications in natural products, pharmaceuticals, and ...
Galdina V. Suárez‐Moreno   +6 more
wiley   +1 more source

Substrate‐Selective Temperature‐Controlled Synthesis of Thiophene Derivatives at Interfaces

open access: yesAngewandte Chemie, Volume 138, Issue 6, 2 February 2026.
The deposition of a dithiophene derivative on Ag(111) at room temperature followed by annealing gives rise to molecular wires, whereas the adsorption of the same precursor on a hot substrate affords the formation of benzotrithiophene species. Abstract The temperature‐controlled transformation of organic molecules at interfaces is an incipient yet ...
Elena Pérez‐Elvira   +16 more
wiley   +2 more sources

Amido‐Imidazolin‐2‐imine Zinc Complexes: Facile Preparation by Mild In Situ Deprotonation

open access: yesZeitschrift für anorganische und allgemeine Chemie, Volume 652, Issue 2, 5 February 2026.
A representative amino‐imidazolin‐2‐imine ligand enables the preparation of stable zinc N,N´‐chelate complexes via in situ deprotonation. This mild method generates only volatile side products and affords both zinc(I) and zinc(II) complexes in good yield and high purity.
Leo Wessel   +5 more
wiley   +1 more source

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