Replication data for "Diverse Approaches for the Difunctionalization of PPH Dendrimers, Precise Versus Stochastic: How Does this Influence Catalytic Performance?"

DOI

This dataset contain all raw datas linked to analysis of synthesized molecules reported in the paper: "Diverse Approaches for the Difunctionalization of PPH Den-drimers. Precise Versus Stochastic: How Does this Influence Catalytic Performance?", published on the journal ACS Macro Letters.

Bruker Topspin, 4.1.1 or higher

MestReNova, 12.0.0 or higher

OriginPro, 8.1 or higher

METHODOLOGICAL INFORMATION: Description of methods used for collection-generation of data: 1H NMR spectra were recorded on Agilent Mercury spectrometers (300 MHz, 400 MHz). Chemical shifts (δ) are reported in parts per million (ppm) downfield from trimethylsilane (TMS) and referred to residual solvent peak: CDCl3 (δH = 7.26 ppm) or DCM-d2 (δH = 5.32 ppm). The spectra were processed using MestReNova software. 13C NMR spectra were recorded at room temperature. Chemical shifts are reported in parts per million downfield from TMS signal and referred to residual peak solvent: CDCl3 (δC = 77.2 ppm) or DCM-d2 (δC = 54.0 ppm). Otherwise stated, the multiplicity refers to 1H decoupled spectra. The spectra were processed using MestReNova software. 19F NMR spectra were recorded at room temperature. Chemical shifts are reported in parts per million. Otherwise stated, the multiplicity refers to 1H decoupled spectra. The spectra were processed using MestReNova software. 31P NMR spectra were recorded at room temperature in CDCl3 or DCM-d2. Chemical shifts are reported in parts per million relative to H3PO4 85% aqueous solution (δP = 0.00 ppm) as an external standard. The spectra were processed using MestReNova software. IR spectra were recorded with on a Bruker Tensor 27 spectrometer fitted with a universal Attenuated Total High-resolution mass spectra (HR-MS) were measured at the Servicio de Espectrometría de Masas at the Universidad de Zaragoza. Elemental Analyses and Inductively coupled plasma (ICP-OES) were measured at the Servei d’Anàlisi Química de l’Universitat Autònoma de Barcelona. Methods for processing the data: NMR and IR are presented Raw. Mass Spectra are presented as a report from Servicio de Espectrometría de Masas at the Universidad de Zaragoza. ICP analyses are presented as a report from the Servei d'Anàlisi Química de la UAB

Identifier
DOI https://doi.org/10.34810/data1787
Related Identifier IsCitedBy https://doi.org/10.1021/acsmacrolett.4c00204
Metadata Access https://dataverse.csuc.cat/oai?verb=GetRecord&metadataPrefix=oai_datacite&identifier=doi:10.34810/data1787
Provenance
Creator Petriccone, Massimo ORCID logo; LAURENT, Régis ORCID logo; Sebastian, Rosa Maria ORCID logo; Caminade, Anne-marie ORCID logo
Publisher CORA.Repositori de Dades de Recerca
Contributor Sebastián Pérez, Rosa Maria; Universitat Autònoma Barcelona
Publication Year 2024
Funding Reference European Commission 860322 ; Agència de Gestió d'Ajuts Universitaris i Recerca 2021/SGR-00064 ; Agència de Gestió d'Ajuts Universitaris i Recerca 2021/SGR-00122 ; Agencia Estatal de Investigación PID2019-106171RB-I00 ; Agencia Estatal de Investigación PID2020-116844RB-C21
Rights CC0 1.0; info:eu-repo/semantics/openAccess; http://creativecommons.org/publicdomain/zero/1.0
OpenAccess true
Contact Sebastián Pérez, Rosa Maria (Universitat Autònoma de Barcelona. Departament de Química)
Representation
Resource Type Aggregate data; Dataset
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Version 1.1
Discipline Chemistry; Natural Sciences