Evidence map›Paper›PMID 39298645›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2024

IPr*

Greta Utecht-Jarzyńska, Shicheng Shi, Pengcheng Gao, Szymon Jarzyński, Md Mahbubur Rahman, Roger Lalancette, Roman Szostak, Michal Szostak

Abstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. IPr**Organometallics · 2025
    Article
  2. Review
  3. Article
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

8 authors.

Greta Utecht-JarzyńskaDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.ORCID https://orcid.org/0000-0003-4444-7544
Shicheng ShiDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.
Pengcheng GaoDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.
Szymon JarzyńskiFaculty of Chemistry, University of Lodz, Tamka 12, Łódź, 91-403, Poland.ORCID https://orcid.org/0000-0002-1558-098X
Md Mahbubur RahmanDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.
Roger LalancetteDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.ORCID https://orcid.org/0000-0002-3470-532X
Roman SzostakDepartment of Chemistry, Wroclaw University, F. Joliot-Curie 14, Wroclaw, 50-383, Poland.ORCID https://orcid.org/0000-0002-5436-7284
Michal SzostakDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, United States.ORCID https://orcid.org/0000-0002-9650-9690

Funding

Catalytic Methods for Organic SynthesisR35GM133326 · NIGMS · RUTGERS THE STATE UNIV OF NJ NEWARK · PI Michal Szostak · 2019 to 2026
$2.7M
Narodowa Agencja Wymiany Akademickiej BPN/BEK/2022/1/00046National Science Foundation 2018753National Science Foundation 2215975National Science Foundation CAREER CHE-1650766NIGMS NIH HHS R35 GM133326NIGMS NIH HHS R35GM133326Wroclawskie Centrum Sieciowo-Superkomputerowe, Politechnika Wroclawska WCSS159
6 · The paper itself

Abstract

The introduction of fluorine atom has attracted considerable interest in molecular design owing to the high electronegativity and the resulting polarization of carbon-fluorine bonds. Simultaneously, sterically-hindered N-heterocyclic carbenes (NHCs) have received major interest due to high stabilization of the reactive metal centers, which has paved the way for the synthesis of stable and reactive organometallic compounds with broad applications in main group chemistry, inorganic synthesis and transition-metal-catalysis. Herein, we report the first class of sterically-hindered, fluorinated N-heterocyclic carbenes. These ligands feature variable fluorine substitution at the N-aromatic wingtip, permitting to rationally vary steric and electronic characteristics of the carbene center imparted by the fluorine atom. An efficient, one-pot synthesis of fluorinated IPr*

Indexed as

Fluorinated NHCsLigand designMetal stabilizationN-heterocyclic carbenes

Identifiers

PMID39298645
PMCPMC12009559

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.