التفاصيل البيبلوغرافية
العنوان: |
Heteroleptic ruthenium(ii) chromophores based on tunable polytopic 4'-(benzamidinato)-2,2':6',2''-terpyridines. |
المؤلفون: |
Cooke MW; Department of Chemistry, Université de Montréal, Québec, H3T 1J4, Canada. garry.hanan@umontreal.ca., Santoni MP, Hasenknopf B, Hanan GS |
المصدر: |
Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2016 Nov 28; Vol. 45 (44), pp. 17850-17858. Date of Electronic Publication: 2016 Oct 24. |
نوع المنشور: |
Journal Article |
اللغة: |
English |
بيانات الدورية: |
Publisher: Royal Society of Chemistry Country of Publication: England NLM ID: 101176026 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1477-9234 (Electronic) Linking ISSN: 14779226 NLM ISO Abbreviation: Dalton Trans Subsets: PubMed not MEDLINE |
أسماء مطبوعة: |
Original Publication: Cambridge, UK : Royal Society of Chemistry, c2003- |
مستخلص: |
A modulable and simple approach towards heteroleptic ruthenium(ii) complexes of amidine-based polypyridine ligands is presented. New complexes 1 and 2 ([(terpyridine)Ru(terpyridine-C 6 H 4 -C(NR)(NHR))] 2+ with R = propyl and R = phenyl derivatives, respectively) were characterized by NMR spectroscopy in solution and by X-ray diffraction, which confirmed the obtention of the (E) stereoisomer alone. Depending on the bulkiness of the R-substituents introduced on the amidine moiety, rotational isomerism around the C-N bond could be observed at r.t. Spectroscopic and electrochemical studies showed that the nature of the R-substituents introduced on the amidine moiety can significantly influence the redox and ground-state acido-basic properties of the complexes, while maintaining their electronic features. This particular tunability of polytopic 4'-(amidinato)-terpyridines offers an interesting perspective for photoactive units in larger multi-functional arrays. |
تواريخ الأحداث: |
Date Created: 20161025 Date Completed: 20180118 Latest Revision: 20180118 |
رمز التحديث: |
20240628 |
DOI: |
10.1039/c6dt03169b |
PMID: |
27774551 |
قاعدة البيانات: |
MEDLINE |