Premium
Synthesis and Structure of Dicyclohexylammonium Tri‐ tert ‐pentoxysilanethiolate and 5‐Aminopentylammonium Tri‐ tert ‐pentoxysilanethiolate
Author(s) -
Baranowska K.,
Chojnacki J.,
Gosiewska M.,
Wojnowski W.
Publication year - 2006
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.200600010
Subject(s) - hydrogen bond , chemistry , ammonium , crystallography , elemental analysis , hydrogen , ion , proton nmr , stereochemistry , molecule , inorganic chemistry , organic chemistry
Tri– tert –pentoxysilanethiol, (EtMe 2 CO) 3 SiSH, reacts with dicyclohexylamine and 1,5–diaminopentane yielding ion‐quadruples connected by hydrogen bonds: [{(C 6 H 11 ) 2 NH 2 } + {(EtMe 2 CO) 3 SiS} − ] 2 ( 1 ) and [{H 2 N–C 5 H 10 –NH 3 } + {(EtMe 2 CO) 3 SiS} − ] 2 ( 2 ). The compounds were characterized by X–ray diffraction, elemental analysis, IR and NMR. Both compounds form dimers, composed of two thiolate anions and two ammonium cations. The dimers have a central core of eight–membered rings built due to the formation of four charge–assisted N + –H··· − S–hydrogen bonds. Additional N + –H···N hydrogen bonds are found in the case of 2 , linking the dimers into infinite two–dimensional sheets.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom