Robustness of thioamide dimer synthon, carbon bonding and thioamide–thioamide stacking in ferrocene-based thiosemicarbazones-Reference-Cited by-同舟云学术

Robustness of thioamide dimer synthon, carbon bonding and thioamide–thioamide stacking in ferrocene-based thiosemicarbazones

Published:2015 Issue:12 Volume:17 Page:2553-2561
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Jawaria Rifat¹²³⁴,Hussain Mazhar¹²³⁴,Shafiq Zahid¹²³⁴,Ahmad Hafiz Badaruddin¹²³⁴,Tahir Muhammad Nawaz⁵⁶⁷,Shad Hazoor Ahmad⁵⁶⁷,Naseer Muhammad Moazzam⁸⁹¹⁰

Affiliation:

1. Institute of Chemical Sciences

2. Organic Chemistry Division

3. Bahauddin Zakariya University

4. Multan 60800, Pakistan

5. Department of Physics

6. University of Sargodha

7. Sargodha, Pakistan

8. Department of Chemistry

9. Quaid-i-Azam University

10. Islamabad 45320, Pakistan

Abstract

The role of thioureas in crystal engineering as robust supramolecular synthons is now recognized, but their analogs, namely thiosemicarbazones/N-iminothioureas, have not received the attention they deserve.

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/CE/C4CE02566K

Reference78 articles.

1. Exploiting Supramolecular Synthons in Designing Gelators Derived from Multiple Drugs

2. Triptycene based organometallic complexes: a new class of acceptor synthons for supramolecular ensembles

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4. Energetic multi-component molecular solids of tetrafluoroterephthalic acid with some aza compounds by strong hydrogen bonds and weak intermolecular interactions of C–H⋯F and C–H⋯O

5. Molecular symmetry and fluorine-containing supramolecular synthons as structure-differentiating agents in some “bridge-flipped” isomeric bis-benzylideneanilines

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