Related Experiment Video
Updated: Jan 6, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Photophysical studies on meta- and para-carboranes containing 1-naphthyl groups
Rachel A Harder1, Thomas D McGurrell1, J A Hugh MacBride1
1Department of Chemistry, Durham University, Lower Mountjoy, Stockton Road, Durham DH1 3LE, UK. m.a.fox@durham.ac.uk.
None:
Four new carboranes, C-(1-naphthyl)-meta-, C,C'-bis(1-naphthyl)-meta-, C-(1-naphthyl)-para- and C,C'-bis(1-naphthyl)-para-carborane, reveal high-energy emissions at 332-343 nm with quantum yields of 21-38% and long lifetimes of 26-31 ns in degassed cyclohexane solutions. The experimental absorption and emission spectra of the mononaphthyl carboranes are successfully simulated by hybrid DFT vibronic calculations. The computed lowest energy excited state (S1) geometries contain non-planar naphthyl groups due to shorter carborane C-aromatic C bonds and steric effects between the bulky naphthyl and carboranyl units. The high energy emissions are also reproduced in polymethylmethacrylate (PMMA) films and as solids. The lower energy emissions in 99 : 1 water : THF suspensions for these four compounds at 385-421 nm show quantum yields of 50-64% and long lifetimes of 28-40 ns. The findings indicate that meta- and para-carborane derivatives can generate different solid-state emissions as reported elsewhere for the intensively researched ortho-carborane analogues.
More Related Videos
12:07Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
12:19Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Related Concept Videos
UV–Vis Spectroscopy: Woodward–Fieser Rules
Spectroscopy of Carboxylic Acid Derivatives
Directing Effect of Substituents: meta-Directing Groups
IR and UV–Vis Spectroscopy of Carboxylic Acids
However, the stretching absorptions for the C=O bond vary depending on the structure of carboxylic acids. The C=O bond of the free carboxylic acids shows a higher stretching frequency, 1760 cm−1, while H-bonded carboxylic acids (dimers) exhibit stretching absorptions at a lower frequency,...
Directing Effect of Substituents: ortho–para-Directing Groups
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds