Cookies helfen uns bei der Bereitstellung unserer Dienste. Durch die Nutzung unserer Dienste erklären Sie sich damit einverstanden, dass wir Cookies setzen.
De En Es
Kundenservice: +49 (0) 551 - 547 24 0

Cuvillier Verlag

30 Jahre Kompetenz im wissenschaftlichen Publizieren
Internationaler Fachverlag für Wissenschaft und Wirtschaft

Cuvillier Verlag

Premiumpartner
De En Es
2019-02-11_banner_durchlaufend_versandkostenfrei_jan-apr Titelbild-leitlinien
Studies of group 13 metal complexes bearing nacnac-mimetic bisheterocyclo methanides and amides

Printausgabe
EUR 72,90

E-Book
EUR 51,03

Studies of group 13 metal complexes bearing nacnac-mimetic bisheterocyclo methanides and amides

David-Raphael Dauer (Autor)

Vorschau

Inhaltsverzeichnis, PDF (91 KB)
Leseprobe, PDF (690 KB)

ISBN-13 (Printausgabe) 9783736993761
ISBN-13 (E-Book) 9783736983762
Sprache Englisch
Seitenanzahl 274
Umschlagkaschierung matt
Auflage 1. Aufl.
Erscheinungsort Göttingen
Promotionsort Göttingen
Erscheinungsdatum 24.10.2016
Allgemeine Einordnung Dissertation
Fachbereiche Chemie
Anorganische Chemie
Schlagwörter diketiminate, nacnac, group 13, aluminium, gallium, X-ray diffraction, crystal structures, NMR spectroscopy, hydrogen bonding, methanides, amides, metal complexes
Beschreibung

The omnipresent monoanionic nacnac ligand enables the stabilisation of main group elements in low oxidation states and is used as supporting ligand in several catalytical applications. Referring to the nacnac ligand’s advantages, in the context of this work new ligand systems should be exploited mimicking those electronic and steric properties.
The desired parent bisheterocyclo methane and amine ligand platforms are consisting of two benzannulated 1,3-azoles, which are C2-connected via either a methylene or an amine spacer. In comparison to the paragon nacnac ligand, formally the imine substituents are fixed to the backbone of the ligand by building up an additional five-membered heterocycle, containing either oxygen or sulfur atoms as additional donor sites. The bridge’s protons can easily be abstracted by reaction with the corresponding group 13 metalorganic reagents to form the monoanionic species, carrying the remaining metal fragment. In analogy to the nacnac ligands, also a coordination motif for the metallated species is expected, wherein the metal centre is chelated by two endocyclic nitrogen donors of the trans-trans aligned ligand.
For future research on corresponding low-valent metallylenes based on these ligand systems, a screening for suitable derivatives and precursors will be approached, wherein the screening involves the variation of the heterocycles, the bridging moiety and the coordinated metal fragments. Thus, the desired bisheterocyclo methanide and amide complexes should achieve the best from two worlds: the stabilisation abilities for future low-valent metal complexes and the reactivity of group 13 metals.