Evidence map›Paper›PMID 41716010›Full record

ArticleInorganic chemistry2026

Preparation and Characterization of Oxalyl Dicyanide.

Sven Ringelband, Theodore Cohen, Frank Tambornino

Abstract read
In one paragraph

Article in Inorganic chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Sven RingelbandDepartment of Chemistry, Philipps-University Marburg, Marburg35043, Germany.
Theodore CohenDepartment of Chemistry, Philipps-University Marburg, Marburg35043, Germany.
Frank TamborninoDepartment of Chemistry, Philipps-University Marburg, Marburg35043, Germany.ORCID 0000-0003-3538-6049

Funding

Deutsche Forschungsgemeinschaft TA 1357/5-1
6 · The paper itself

Abstract

Oxalyl dicyanide and its 1,4-dioxane adduct were obtained as colorless crystalline solids from the reaction of oxalyl chloride with trimethylsilyl cyanide. Their crystal structures and vibrational spectra, supported by quantum chemical calculations, are presented. In the solid state, oxalyl dicyanide adopts C2h symmetry with the preferred trans-anti configuration. The 13C NMR spectrum shows two distinct resonances at 159.8 and 109.9 ppm, while characteristic ν(C≡N) and ν(C═O) stretching vibrations are observed at 2243 and 1734 cm-1, respectively. Hydrolysis proceeds rapidly to oxalic acid and hydrogen cyanide, with transient formation of the unusual tetraol 2,2,3,3-tetrahydroxysuccinonitrile, as confirmed by single-crystal X-ray diffraction.

Identifiers

PMID41716010
PMCPMC13439657

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Registered trials

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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.