Two Polymorphs of a Chiral Boranil Dye

Abstract The chiral Boranil dye (LB(O)-Br) exhibits polymorphism forming two distinctly different structures in the solid state. Polymorph I crystallises in the space group I 4 1 / a and exhibits C-H‧‧‧O and C-H‧‧‧Br interactions to produce a columnar structure with 3D connectivity. Polymorph II crystallises in P 2 1 / c and, in addition to C-H‧‧‧O contacts, forms Br‧‧‧O halogen bonds and edge-to-face π-interactions to give a 2D layered structure. Given the propensity of these compounds to fluoresce in the crystalline state, polymorphism of these structures is an important factor to consider when designing dyes of this kind for solid-state applications. Graphical abstract An overlay highlights the areas of the title molecule and its analogue that vary most in terms of conformation.

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Publication Details

Journal
Journal of Chemical Crystallography
Published
2025-11-14
DOI
https://doi.org/10.1007/s10870-025-01070-5
Primary Topic
Crystallography and molecular interactions
Type
article
Field-Weighted Citation Impact
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article

Two Polymorphs of a Chiral Boranil Dye

Julian G. Knight, Nawaf Algoazy, Paul Gordon Waddell
Journal of Chemical Crystallography
Crystallography and molecular interactions
article

Two Polymorphs of a Chiral Boranil Dye

Julian G. Knight, Nawaf Algoazy, Paul Gordon Waddell
article en

Abstract

Abstract The chiral Boranil dye (LB(O)-Br) exhibits polymorphism forming two distinctly different structures in the solid state. Polymorph I crystallises in the space group I 4 1 / a and exhibits C-H‧‧‧O and C-H‧‧‧Br interactions to produce a columnar structure with 3D connectivity. Polymorph II crystallises in P 2 1 / c and, in addition to C-H‧‧‧O contacts, forms Br‧‧‧O halogen bonds and edge-to-face π-interactions to give a 2D layered structure. Given the propensity of these compounds to fluoresce in the crystalline state, polymorphism of these structures is an important factor to consider when designing dyes of this kind for solid-state applications. Graphical abstract An overlay highlights the areas of the title molecule and its analogue that vary most in terms of conformation.

Journal of Chemical CrystallographyVol. 56(1)
Newcastle University (GB)
Openalex Percentile: Top 69%
Crystallography and molecular interactions
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