5 years ago

Synthetic, spectroscopic and structural behavior of unsaturated functionalized N-heterocyclic carbene complexes of group 11

Synthetic, spectroscopic and structural behavior of unsaturated functionalized N-heterocyclic carbene complexes of group 11
A series of unsaturated functionalized silver(I) N-heterocyclic carbenes [{(κC-C7N2H10)AgCl}2] (1a), [{(κC-C8N2H12)2}2Ag][Ag2Cl4] (1b), [{(κC-C9N2H14)2Ag}2][Ag2Cl4] (1c), and [{(κC-C12N2H14)2Ag}2][Ag2Cl4] (1d) have been synthesized and used as transmetalation agents to form the corresponding Au(I) and Cu(I) complexes. The reactions of 1a-d with [Au(SMe2)Cl] or CuI produced the mixed-metal biscarbene compounds [(κC-C7N2H10)2M][AgCl2] (M=Au 2a; Cu 3a), [{(κC-C8N2H12)2}2M][Ag2Cl4] (M=Au 2b; Cu 3b), [{(κC-C9N2H14)2M}2][Ag2Cl4] (M=Au 2c; Cu 3c), and [{(κC-C12N2H14)2}2M][Ag2Cl4] (M=Au 2d; Cu 3d). The carbene complexes were fully characterized by IR, NMR and mass spectrometry, and the molecular structures of 1a, 1b, 2b and the imidazolium salt [PMIM][PF6] (L2′) were determined by single crystal X-ray diffraction studies. Compounds L4, 1d and 2d were used as monomeric units to carry out free-radical polymerization (FRP) reactions using AIBN as initiator.

Publisher URL: www.sciencedirect.com/science

DOI: S0277538717305338

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.