Cooperative Halogen Bonding and <i>π</i> – <i>π</i> Stacking Interactions as Drivers of Polymorphism

Understanding the mechanisms underlying the formation of different polymorphic forms of a given compound is a fundamental issue in modern physical chemistry, with significant implications for the design of functional materials, including those with pharmaceutical relevance. In the present study, the formation of two polymorphic forms of a polyyne compound is elucidated, as confirmed by X-ray crystallographic analysis. The emergence of these polymorphs results from a delicate interplay between halogen bonding and a network of noncovalent π-π stacking interactions. A combination of experimental techniques, single-crystal X-ray diffraction, and theoretical studies allows us to construct a coherent model that rationalizes the formation of both polymorphic modifications of the investigated system.

Authors

Institutions

Publication Details

Journal
ChemPhysChem
Published
2025-10-14
DOI
https://doi.org/10.1002/cphc.202500491
Primary Topic
Crystallography and molecular interactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cooperative Halogen Bonding and π – π Stacking Interactions as Drivers of Polymorphism

Marcin Małecki, Monika Moskwa, Sławomir Szafert, Przemysław Dopieralski
ChemPhysChem
Crystallography and molecular interactions
article

Cooperative Halogen Bonding and π – π Stacking Interactions as Drivers of Polymorphism

Marcin Małecki, Monika Moskwa, Sławomir Szafert, Przemysław Dopieralski
article en

Abstract

Understanding the mechanisms underlying the formation of different polymorphic forms of a given compound is a fundamental issue in modern physical chemistry, with significant implications for the design of functional materials, including those with pharmaceutical relevance. In the present study, the formation of two polymorphic forms of a polyyne compound is elucidated, as confirmed by X-ray crystallographic analysis. The emergence of these polymorphs results from a delicate interplay between halogen bonding and a network of noncovalent π-π stacking interactions. A combination of experimental techniques, single-crystal X-ray diffraction, and theoretical studies allows us to construct a coherent model that rationalizes the formation of both polymorphic modifications of the investigated system.

ChemPhysChemVol. 26(22)
University of Wrocław (PL), Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry (CZ)
Openalex Percentile: Top 73%
Crystallography and molecular interactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Cooperative Halogen Bonding and <i>π</i> – <i>π</i> Stacking Interactions as Drivers of Polymorphism — Marcin Małecki, Monika Moskwa, et al. · ChemPhysChem (2025) | TGRS Research Map | TGRS