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Bis[5-(anthracen-9-ylmeth-yl)-1,5,9-tri-aza-cyclododecan-1-ium] tetra-chlorido-zincate.

アントラセン基を有するポリアミン配位子と四塩化亜鉛アニオンからなる結晶性塩の構造解析

other not specified not assessed

Abstract

A crystalline salt consisting of two monoprotonated 12-membered polyamine macrocycle cations bearing anthracen-9-ylmethyl pendant arms and one tetrachloridozincate(II) anion was synthesized and characterized by single-crystal X-ray diffraction. The protonated nitrogen centers formed intramolecular hydrogen bonds with neighboring nitrogen atoms within the macrocyclic framework. In the solid state, the pendant anthracene moieties engaged in intermolecular π-π stacking and C-H⋯π interactions, which were identified as key contributors to crystal cohesion. Structural comparisons were drawn with related compounds featuring different macrocyclic ring sizes and pendant substituents, providing insight into how framework variation influences supramolecular packing.

Bibliographic

Authors
Ichimaru Y, Kato K, Jin W, Kurihara M, Kurosaki H
Journal
IUCrdata
Year
2025
PMID
40487511
DOI
10.1107/S2414314625003566
PMC
PMC12142395

Delivery context

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

Safety notes

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

See also:

Cite as: H2 Papers — PMID 40487511. https://h2-papers.org/en/papers/40487511
Source: PubMed PMID 40487511