Chemistry of Diruthenium and Dirhodium Analogues of Pentaborane(9): Synthesis and Characterization of Metal N, S‐Heterocyclic Carbene and B‐Agostic Complexes. Issue 9 (23rd December 2014)
- Record Type:
- Journal Article
- Title:
- Chemistry of Diruthenium and Dirhodium Analogues of Pentaborane(9): Synthesis and Characterization of Metal N, S‐Heterocyclic Carbene and B‐Agostic Complexes. Issue 9 (23rd December 2014)
- Main Title:
- Chemistry of Diruthenium and Dirhodium Analogues of Pentaborane(9): Synthesis and Characterization of Metal N, S‐Heterocyclic Carbene and B‐Agostic Complexes
- Authors:
- Roy, Dipak Kumar
Mondal, Bijan
Anju, R. S.
Ghosh, Sundargopal - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Building upon our earlier results on the synthesis of electron‐precise transition‐metal–boron complexes, we continue to investigate the reactivity of pentaborane(9) and tetraborane(10) analogues of ruthenium and rhodium towards thiazolyl and oxazolyl ligands. Thus, mild thermolysis of <italic>nido</italic>‐[(Cp*RuH)<sub>2</sub>B<sub>3</sub>H<sub>7</sub>] (<bold>1</bold>) with 2‐mercaptobenzothiazole (2‐mbtz) and 2‐mercaptobenzoxazole (2‐mboz) led to the isolation of Cp*‐based (Cp*=η<sup>5</sup>‐C<sub>5</sub>Me<sub>5</sub>) borate complexes <bold>5 a</bold>, <bold>b</bold> [Cp*RuBH<sub>3</sub>L] (<bold>5 a</bold>: L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>; <bold>5 b</bold>: L=C<sub>7</sub>H<sub>4</sub>NOS)) and agostic complexes <bold>7 a</bold>, <bold>b</bold> [Cp*RuBH<sub>2</sub>(L)<sub>2</sub>], (<bold>7 a</bold>: L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>; <bold>7 b</bold>: L=C<sub>7</sub>H<sub>4</sub>NOS). In a similar fashion, a rhodium analogue of pentaborane(9), <italic>nido</italic>‐[(Cp*Rh)<sub>2</sub>B<sub>3</sub>H<sub>7</sub>] (<bold>2</bold>) yielded rhodaboratrane [Cp*RhBH(L)<sub>2</sub>], <bold>10</bold> (L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>). Interestingly, when the reaction was performed with an excess of 2‐mbtz, it led to the formation of the first structurally characterized N, S‐heterocyclic rhodium‐carbene complex [(Cp*Rh)(L<sub>2</sub>)(1‐benzothiazol‐2‐ylidene)]<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Building upon our earlier results on the synthesis of electron‐precise transition‐metal–boron complexes, we continue to investigate the reactivity of pentaborane(9) and tetraborane(10) analogues of ruthenium and rhodium towards thiazolyl and oxazolyl ligands. Thus, mild thermolysis of <italic>nido</italic>‐[(Cp*RuH)<sub>2</sub>B<sub>3</sub>H<sub>7</sub>] (<bold>1</bold>) with 2‐mercaptobenzothiazole (2‐mbtz) and 2‐mercaptobenzoxazole (2‐mboz) led to the isolation of Cp*‐based (Cp*=η<sup>5</sup>‐C<sub>5</sub>Me<sub>5</sub>) borate complexes <bold>5 a</bold>, <bold>b</bold> [Cp*RuBH<sub>3</sub>L] (<bold>5 a</bold>: L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>; <bold>5 b</bold>: L=C<sub>7</sub>H<sub>4</sub>NOS)) and agostic complexes <bold>7 a</bold>, <bold>b</bold> [Cp*RuBH<sub>2</sub>(L)<sub>2</sub>], (<bold>7 a</bold>: L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>; <bold>7 b</bold>: L=C<sub>7</sub>H<sub>4</sub>NOS). In a similar fashion, a rhodium analogue of pentaborane(9), <italic>nido</italic>‐[(Cp*Rh)<sub>2</sub>B<sub>3</sub>H<sub>7</sub>] (<bold>2</bold>) yielded rhodaboratrane [Cp*RhBH(L)<sub>2</sub>], <bold>10</bold> (L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>). Interestingly, when the reaction was performed with an excess of 2‐mbtz, it led to the formation of the first structurally characterized N, S‐heterocyclic rhodium‐carbene complex [(Cp*Rh)(L<sub>2</sub>)(1‐benzothiazol‐2‐ylidene)] (<bold>11</bold>) (L=C<sub>7</sub>H<sub>4</sub>NS<sub>2</sub>). Furthermore, to evaluate the scope of this new route, we extended this chemistry towards the diruthenium analogue of tetraborane(10), <italic>arachno</italic>‐[(Cp*RuCO)<sub>2</sub>B<sub>2</sub>H<sub>6</sub>] (<bold>3</bold>), in which the metal center possesses different ancillary ligands.</p> </abstract> … (more)
- Is Part Of:
- Chemistry. Volume 21:Issue 9(2015)
- Journal:
- Chemistry
- Issue:
- Volume 21:Issue 9(2015)
- Issue Display:
- Volume 21, Issue 9 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 9
- Issue Sort Value:
- 2015-0021-0009-0000
- Page Start:
- 3640
- Page End:
- 3648
- Publication Date:
- 2014-12-23
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201405218 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4017.xml