At the dated check, the references listed below either did not resolve in
Crossref or DataCite, or carried a retraction notice. Each one is shown with the
registry record that put it there.
The 37 checked references that resolve
resolves10.1021/ja001179gEfficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
resolves10.1021/cr800524fRuthenium-Based Olefin Metathesis Catalysts Bearing <i>N</i>-Heterocyclic Carbene Ligands
resolves10.1021/cr9002424Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
resolves10.1021/ja048794vNitro-Substituted Hoveyda−Grubbs Ruthenium Carbenes: Enhancement of Catalyst Activity through Electronic Activation
resolves10.1039/b311496cRu complexes bearing bidentate carbenes: from innocent curiosity to uniquely effective catalysts for olefin metathesis
resolves10.1021/ja900067cEffects of NHC-Backbone Substitution on Efficiency in Ruthenium-Based Olefin Metathesis
resolves10.1021/om0109206Preparation and Activity of Recyclable Polymer-Supported Ruthenium Olefin Metathesis Catalysts
resolves10.1039/b007304kOlefin metathesis in non-degassed solvent using a recyclable, polymer supported alkylideneruthenium
resolves10.1021/ol802728tPolyisobutylene-Anchored <i>N</i>-Heterocyclic Carbene Ligands
resolves10.1021/om021007nNew Soluble-Polymer Bound Ruthenium Carbene Catalysts: Synthesis, Characterization, and Application to Ring-Closing Metathesis
resolves10.1016/j.jorganchem.2005.03.031An ionic liquid-tagged second generation Hoveyda–Grubbs ruthenium carbene complex as highly reactive and recyclable catalyst for ring-closing metathesis of di-, tri- and tetrasubstituted dienes
resolves10.1039/b705451cHighly recoverable pyridinium-tagged Hoveyda–Grubbs pre-catalyst for olefin metathesis. Design of the boomerang ligand toward the optimal compromise between activity and reusability
resolves10.1021/ol7016774Self-Supported Oligomeric Grubbs/Hoveyda-Type Ru−Carbene Complexes for Ring-Closing Metathesis
resolves10.1002/ejoc.200900407Towards Long‐Living Metathesis Catalysts by Tuning the N‐Heterocyclic Carbene (NHC) Ligand on Trifluoroacetamide‐Activated Boomerang Ru Complexes
resolves10.1021/ja0302228Chiral Ru-Based Complexes for Asymmetric Olefin Metathesis: Enhancement of Catalyst Activity through Steric and Electronic Modifications
resolves10.1002/chem.200701340In an Attempt to Provide a User's Guide to the Galaxy of Benzylidene, Alkoxybenzylidene, and Indenylidene Ruthenium Olefin Metathesis Catalysts
resolves10.1021/ja807717sInitial Catalyst−Substrate Association Step in Enyne Metathesis Catalyzed by Grubbs Ruthenium Complex Probed by Time-Dependent Fluorescence Quenching
resolves10.1021/om800228vToward the Single-Molecule Investigation of Organometallic Reaction Mechanisms: Single-Molecule Imaging of Fluorophore-Tagged Palladium(II) Complexes
resolves10.1002/ange.200604965Einzelmolekülfluoreszenzspektroskopische Beobachtung der Bildung und des Zerfalls individueller Metallkomplexe
resolves10.1002/anie.200604965Direct Monitoring of Formation and Dissociation of Individual Metal Complexes by Single‐Molecule Fluorescence Spectroscopy
resolves10.1002/chem.200903275[(NHC)(NHC<sub>ewg</sub>)RuCl<sub>2</sub>(CHPh)] Complexes with Modified NHC<sub>ewg</sub> Ligands for Efficient Ring‐Closing Metathesis Leading to Tetrasubstituted Olefins
resolves10.1016/S0040-4020(03)01029-9Ruthenium olefin metathesis catalysts with modified styrene ethers: influence of steric and electronic effects
resolves10.1021/cr00002a004A survey of Hammett substituent constants and resonance and field parameters
resolves10.1002/ange.201000581Probing the Mechanism of Olefin Metathesis in Grubbs–Hoveyda and Grela Type Complexes
resolves10.1002/anie.201000581Probing the Mechanism of Olefin Metathesis in Grubbs–Hoveyda and Grela Type Complexes
resolves10.1021/ja903554vImpact of NHC Ligand Conformation and Solvent Concentration on the Ruthenium-Catalyzed Ring-Closing Metathesis Reaction
The 9 references without a DOI — listed, not checked
no DOI — not checked
no DOI — not checked
no DOI — not checked
no DOI — not checked
no DOI — not checkede_1_2_3_17_2
no DOI — not checked
no DOI — not checkedThis experiment was done immediately after the first experiment under precisely the same experimental conditions as the blank experiment in order to enable comparision of absolute fluorescence intensities.
no DOI — not checkedIt was not possible to precisely correlate the fluorescence intensity with the amount of liberated fluorophore as the fluorescence intensity is changed by the presence of ruthenium complex.
no DOI — not checkedWith a large of amount of precatalyst and a comparatively low amount of active species decomposition reactions originating from the active species will be less relevant.
checked 2026-07-23 — re-checked daily as this page is visited;
titles and statuses come from Crossref and DataCite and are not part of the signed record
Both snippets point at the live badge image and link back to this page. The
badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.