Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process
<p>Researchers use metal-thiophene complexes to mimic reactions which occur inside hydrodesulfurization (HDS) reactors. Information obtained from these model studies may often be applied to understanding the mechanisms involved with commercially used catalysts. Certain mechanisms<sup>1&l...
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ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-449462021-05-15T05:26:34Z Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process Grieb, Arthur L. Chemistry Merola, Joseph S. Hanson, Brian E. Anderson, Mark R. LD5655.V855 1993.G753 Feed processing Petroleum -- Refining -- Desulfurization Thiophenes <p>Researchers use metal-thiophene complexes to mimic reactions which occur inside hydrodesulfurization (HDS) reactors. Information obtained from these model studies may often be applied to understanding the mechanisms involved with commercially used catalysts. Certain mechanisms<sup>1</sup> for HDS propose thiophene ring cleavage,forming a metallacycle, prior to hydrogenation of one double bond. There are, however, limited examples of complexes derived from C-S cleavage.<sup>2,3,4</sup></p> <p> Thermal reactions of the iridium complex, [Ir(COD)(PMe<sub>3)3</sub>]Cl (COD=1,5- cyclooctadiene), with thiophene, thiazole, 4-methyl thiazole and 5-methyl thiazole yields the C-S addition metallacycles (Me<sub>3</sub>P)<sub>3</sub>Ir-(CH=CHCH=S)CI (I), \ (Me3P)3Ir-(CH=NCH=CHS)CI (II), (Me3P)3Ir-CCH=NC(CH3)=CHS)CI (III) and (Me3P)3Ir (CH=NCH=C(CH3)S)CI (IV), respectively. These compounds were characterized using the following methods: <sup>1</sup> H NMR, <sup>13</sup>C NMR, <sup>31</sup> P NMR, elemental analysis and single crystal x-ray diffraction.</p> <p> Following C-S addition to [Ir(COD)(PMe3)3]CI, nitrogen present in the thiazoles exhibit enhanced nucleophilicity. For exmnple, compounds II-IV react with methylene chloride to form dimers: CH2[NCR=CR'SIr(Cl)(PMe3)3CH]2. The above compounds are soluble in water and react with PF6 salts liberating the chloride atom from the Ir center. pKb measurements were recorded as well.</p> <p> This thesis describes the synthesis and examination of con1pounds I-IV as they may model the HDS process. Compounds II-IV represent the first examples of ring opened thiazole metallacycles with iridium.</p> Master of Science 2014-03-14T21:46:38Z 2014-03-14T21:46:38Z 1993-08-05 2009-09-29 2009-09-29 2009-09-29 Thesis Text etd-09292009-020335 http://hdl.handle.net/10919/44946 http://scholar.lib.vt.edu/theses/available/etd-09292009-020335/ en OCLC# 29323336 LD5655.V855_1993.G753.pdf In Copyright http://rightsstatements.org/vocab/InC/1.0/ v, 57 leaves BTD application/pdf application/pdf Virginia Tech |
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LD5655.V855 1993.G753 Feed processing Petroleum -- Refining -- Desulfurization Thiophenes Grieb, Arthur L. Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
description |
<p>Researchers use metal-thiophene complexes to mimic reactions which occur
inside hydrodesulfurization (HDS) reactors. Information obtained from these model
studies may often be applied to understanding the mechanisms involved with
commercially used catalysts. Certain mechanisms<sup>1</sup> for HDS propose thiophene ring
cleavage,forming a metallacycle, prior to hydrogenation of one double bond. There are,
however, limited examples of complexes derived from C-S cleavage.<sup>2,3,4</sup></p>
<p>
Thermal reactions of the iridium complex, [Ir(COD)(PMe<sub>3)3</sub>]Cl (COD=1,5-
cyclooctadiene), with thiophene, thiazole, 4-methyl thiazole and 5-methyl thiazole yields
the C-S addition metallacycles (Me<sub>3</sub>P)<sub>3</sub>Ir-(CH=CHCH=S)CI (I), \
(Me3P)3Ir-(CH=NCH=CHS)CI (II), (Me3P)3Ir-CCH=NC(CH3)=CHS)CI (III) and (Me3P)3Ir (CH=NCH=C(CH3)S)CI (IV), respectively.
These compounds were characterized using
the following methods: <sup>1</sup> H NMR, <sup>13</sup>C NMR, <sup>31</sup> P NMR, elemental analysis and single
crystal x-ray diffraction.</p>
<p>
Following C-S addition to [Ir(COD)(PMe3)3]CI, nitrogen present in the thiazoles
exhibit enhanced nucleophilicity. For exmnple, compounds II-IV react with methylene
chloride to form dimers: CH2[NCR=CR'SIr(Cl)(PMe3)3CH]2. The above compounds
are soluble in water and react with PF6 salts liberating the chloride atom from the Ir
center. pKb measurements were recorded as well.</p>
<p>
This thesis describes the synthesis and examination of con1pounds I-IV as they
may model the HDS process. Compounds II-IV represent the first examples of ring opened
thiazole metallacycles with iridium.</p> === Master of Science |
author2 |
Chemistry |
author_facet |
Chemistry Grieb, Arthur L. |
author |
Grieb, Arthur L. |
author_sort |
Grieb, Arthur L. |
title |
Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
title_short |
Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
title_full |
Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
title_fullStr |
Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
title_full_unstemmed |
Synthesis and characterization of Ir(III) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
title_sort |
synthesis and characterization of ir(iii) metallacycles derived from thiophene and related compounds: models for the hydrodesulfurization process |
publisher |
Virginia Tech |
publishDate |
2014 |
url |
http://hdl.handle.net/10919/44946 http://scholar.lib.vt.edu/theses/available/etd-09292009-020335/ |
work_keys_str_mv |
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