In this work, we conducted a comparative analysis of the metal ion sensing capabilities of two pyridine-end oligo p-phenylenevinylene compounds featuring different alkyl substituents (-C4H9 and -C16H33) within a micelle medium. Our findings reveal...
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Alkoxylated Fluoranthene‐Fused [3.3.3]Propellanes: Facile Film Formation against High π‐Core Content
Von Wiley-VCH zur Verfügung gestellt
Structural, thermal, and optical properties reveal that amorphous assembling is easily attained in a series of fluoranthene-fused [3.3.3]propellanes with a rigid 3D skeleton bearing n-butoxy or longer alkoxy groups. Drop-cast films can be obtained despite the high D 3h molecular symmetry and high ratios of π-core atoms to peripheral rotatable ones.
Abstract
Solid-state assembling modes are as crucial as the chemical structures of single molecules for real applications. In this work, solid-state structures and phase-transition temperatures are investigated for a series of fluoranthene-fused [3.3.3]propellanes consisting of a rigid three-dimensional (3D) π-core and varying lengths of alkoxy groups. Compounds in this series with n-butoxy or longer alkoxy groups take an amorphous state at room temperature. In these molecules, rotatable biaryl-type bonds are not incorporated and high D 3h molecular symmetry is retained. Therefore, π-fused [3.3.3]propellanes present a unique platform for amorphous molecular materials with low ratios of flexible alkoxy atoms to rigid π-core ones.
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