ArticleChemistry (Weinheim an der Bergstrasse, Germany)2026
Self-Complementary Dimers Based on Zwitterionic Halogen Bond Donors.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
Abstract
Even though halogen bonding is routinely used in crystal engineering and beyond, motifs offering multipoint interactions are still rare. This applies in particular to self-complementary systems which incorporate both halogen bond donating and accepting moieties. In this study, we present the first isolated homodimers based on a zwitterionic halogen bond donor, in which an iodolium core acts as Lewis acidic unit and a sulfonate group acts as Lewis base. Initial experiments with a carboxylate variant featured too strong coordination, leading to poor solubility. The optimized sulfonate systems, in contrast, resulted in strongly bound dimers with halogen bond distances of up to 2.73 Å. We anticipate this motif to form the basis for the further development of halogen-bonding-based linkers.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.