Potential Impact of Substituents on the Crystal Structures and Properties of Tl(I) Ferrocenyl/Picolyl‐Functionalized Dithiocarbamates; Tl⋯H‐CAnagostic Interactions. Issue 18 (14th November 2016)
- Record Type:
- Journal Article
- Title:
- Potential Impact of Substituents on the Crystal Structures and Properties of Tl(I) Ferrocenyl/Picolyl‐Functionalized Dithiocarbamates; Tl⋯H‐CAnagostic Interactions. Issue 18 (14th November 2016)
- Main Title:
- Potential Impact of Substituents on the Crystal Structures and Properties of Tl(I) Ferrocenyl/Picolyl‐Functionalized Dithiocarbamates; Tl⋯H‐CAnagostic Interactions
- Authors:
- Manar, Krishna K.
Rajput, Gunjan
Yadav, Manoj K.
Yadav, Chote L.
Kumari, Kavita
Drew, Michael G. B.
Singh, Nanhai - Abstract:
- Abstract: New ferrocenyl/pyridyl functionalized dithiocarbamate complexes, [Tl(dtc)]∞ (dtc=(N‐ferrocenyl‐N‐2‐methylpyridyl) dithiocarbamate (L1)1, (N‐ferrocenyl‐N‐methyl) dithiocarbamate (L2)2, (N‐methylthiophene‐N‐3‐methylpyridyl) dithiocarbamate (L3)3, (N‐4‐chlorobenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L4)4 and (N‐4‐methylbenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L5)5 ) have been synthesized and characterized by elemental analyses, IR, UV‐Vis., 1 H and 13 C { 1 H} NMR spectroscopy. Their crystal structures revealed polymeric structures based on dimeric [Tl(dtc)]2 scaffolds which are linked via Tl⋯Tl, Tl‐N(Py) and Tl⋯S bonds and rare C−H⋯Tl anagostic, C–S⋯Tl, Tl⋯N(dtc), Tl⋯C and Tl⋯π(arene) intermolecular bonding interactions which have been assessed by theoretical calculations.The supramolecular structures in these complexes have been sustained by weak C−H⋯S, C−H⋯N, C−H⋯Cl, C−H⋯π, π⋯ π and H⋯H interactions. Except for1 and2 having ferrocene groups as quenchers, all the complexes show luminescent characteristics in the solid phase. Complexes1–5 are weakly conducting (σrt, 10 −4 ‐10 −7 S cm −1, Ea=0.89‐1.00 eV) but show semiconducting behavior in the solid state. The TGA decomposition products of1—5 revealed formation of binary TlS and ternary Fe2 Tl4 S5 and Fe3 Tl2 S4 sulfide materials. Abstract : Influence of ferrocenyl/picolyl functionalities on the structure and properties of [Tl(dtc)]∞ (dtc=(N‐ferrocenyl‐N‐2‐methylpyridyl) dithiocarbamate (L1)1,Abstract: New ferrocenyl/pyridyl functionalized dithiocarbamate complexes, [Tl(dtc)]∞ (dtc=(N‐ferrocenyl‐N‐2‐methylpyridyl) dithiocarbamate (L1)1, (N‐ferrocenyl‐N‐methyl) dithiocarbamate (L2)2, (N‐methylthiophene‐N‐3‐methylpyridyl) dithiocarbamate (L3)3, (N‐4‐chlorobenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L4)4 and (N‐4‐methylbenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L5)5 ) have been synthesized and characterized by elemental analyses, IR, UV‐Vis., 1 H and 13 C { 1 H} NMR spectroscopy. Their crystal structures revealed polymeric structures based on dimeric [Tl(dtc)]2 scaffolds which are linked via Tl⋯Tl, Tl‐N(Py) and Tl⋯S bonds and rare C−H⋯Tl anagostic, C–S⋯Tl, Tl⋯N(dtc), Tl⋯C and Tl⋯π(arene) intermolecular bonding interactions which have been assessed by theoretical calculations.The supramolecular structures in these complexes have been sustained by weak C−H⋯S, C−H⋯N, C−H⋯Cl, C−H⋯π, π⋯ π and H⋯H interactions. Except for1 and2 having ferrocene groups as quenchers, all the complexes show luminescent characteristics in the solid phase. Complexes1–5 are weakly conducting (σrt, 10 −4 ‐10 −7 S cm −1, Ea=0.89‐1.00 eV) but show semiconducting behavior in the solid state. The TGA decomposition products of1—5 revealed formation of binary TlS and ternary Fe2 Tl4 S5 and Fe3 Tl2 S4 sulfide materials. Abstract : Influence of ferrocenyl/picolyl functionalities on the structure and properties of [Tl(dtc)]∞ (dtc=(N‐ferrocenyl‐N‐2‐methylpyridyl) dithiocarbamate (L1)1, (N‐ferrocenyl‐N‐methyl) dithiocarbamate (L2)2, (N‐methylthiophene‐N‐3‐methylpyridyl) dithiocarbamate (L3)3, (N‐4‐chlorobenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L4)4 and (N‐4‐methylbenzyl‐N‐3‐methylpyridyl) dithiocarbamate (L5)5 ). X‐ray crystal structures revealed existence of rare C−H⋯Tl intermolecular anagostic, Tl⋯N(dtc), Tl⋯π(arene) and C−S⋯Tl interactions in these complexes which have been supported by theoretical calculations. They show luminescent and solid phase conducting characteristics. … (more)
- Is Part Of:
- ChemistrySelect. Volume 1:Issue 18(2016)
- Journal:
- ChemistrySelect
- Issue:
- Volume 1:Issue 18(2016)
- Issue Display:
- Volume 1, Issue 18 (2016)
- Year:
- 2016
- Volume:
- 1
- Issue:
- 18
- Issue Sort Value:
- 2016-0001-0018-0000
- Page Start:
- 5733
- Page End:
- 5742
- Publication Date:
- 2016-11-14
- Subjects:
- Luminescent -- Semiconducting -- Tl(I) dithiocarbamates -- TGA -- Tl⋯H−C anagostic interactions
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.201601280 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
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- Legaldeposit
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- British Library DSC - 3172.241000
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