9-BBN hydroborate complexes Ti{(mu-H)2BC8H14}3(THF)2 (1), Ti{(mu-H)2BC8H14}3(OEt2) (2), and [K(OEt2)4]-[Ti{(mu-H)2BC8H14}4] (4) were formed from the reaction of TiCl4 with K[H2BC8H14] in diethyl ether or THF. Ti{(mu-H)2BC8H14}3(PhNH2) (3) was isolated from the reaction of 2 with aniline in diethyl ether. In the formation of these complexes, Ti(IV) is reduced to Ti(III). The coordinated diethyl ether in 2 can be displaced by the stronger bases THF and aniline, to form 1 and 3, respectively. All of the compounds were characterized by single-crystal X-ray diffraction analysis. In complex 1, which contains two coordinated THF ligands, the titanium possesses a 17 electron configuration and there is no evidence for agostic interaction. Complexes 2 and 3 contain only one coordinated ether or aniline ligand, and the titanium possesses a 15 electron configuration. In these compounds, a C-H hydrogen on an alpha carbon on the BC8H14 unit of a 9-BBN hydroborate ligand forms an agostic interaction with the titanium. Criteria for assessing the existence of agostic interactions are discussed. As the potassium salt, the anion of complex 4 is more stable than the complexes 1-3. Organometallic anions of the type [ML4]- for titanium(III) are rare.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ic050422fDOI Listing

Publication Analysis

Top Keywords

9-bbn hydroborate
12
diethyl ether
12
hydroborate complexes
8
agostic interactions
8
titanium possesses
8
possesses electron
8
electron configuration
8
agostic interaction
8
complexes
5
preparation crystal
4

Similar Publications

-Ge/B 1,1-Hydroboration of Alkynylgermanes with 9-BBN.

Org Lett

January 2025

Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.

A 1,1-hydroboration of alkynylgermanes with unique -Ge/B stereochemistry under transition-metal-free conditions is reported. Mechanistic studies suggest that a pathway involving α-boration followed by a stepwise 1,2-Ge/H shift on the intermediate structurally lies between an alkyne-Ge π complex and a typical vinyl cation. The resulting Ge/B bimetallic modules, along with a /Ge/B trimetallic variant, can be conveniently transformed into trisubstituted olefins through iterative divergent cross-coupling.

View Article and Find Full Text PDF

We experimentally demonstrate a new type of the intramolecular reaction between non-activated alkyne units and the dialkylboryl group (9-BBN), which was previously only hypothesized and studied on a calculational level. The reaction described here can formally be classified as a 1,2-hydroboration reaction, but, in contrast to the classical mechanism via a cyclic four-membered transition state, the reaction proceeds by a pericyclic mechanism involving a six-membered transition state. In practice, the reaction allows the synthesis of a new class of the borolenes fused with silole or dihydrosilole units.

View Article and Find Full Text PDF

The selective double hydroboration of CO into bis(boryl)acetal (BBA) is a challenging yet appealing reduction process since BBA can be used as a versatile C and C sources for the synthesis of value-added products. In the present study, we demonstrate that simple borohydride compounds are efficient and selective catalysts for the synthesis of BBA when using 9-borabicyclo(3.3.

View Article and Find Full Text PDF

Zinc-Catalyzed Hydroboration of Carbon Dioxide Amplified by Borane-Tethered Heteroscorpionate Bis(Pyrazolyl)methane Ligands.

Inorg Chem

May 2024

Centro de Química Estrutural, Institute of Molecular Sciences, Departamento de Engenharia Química, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049 001 Lisboa, Portugal.

The borane-functionalized (BR) bis(3,5-dimethylpyrazolyl)methane () ligands (BR: 9-borabicyclo[3.3.1]nonane or 9-BBN), (BR: BCy), and (BR: B(CF)) were synthesized by the allylation-hydroboration of .

View Article and Find Full Text PDF
Article Synopsis
  • Thorium complexes with specially designed heterocyclic iminato ligands were synthesized and shown to effectively hydroborate organic carbonates, producing boronated diols and methanol.
  • The process involves breaking down carbon monoxide to yield methanol and other products, highlighting the potential for recycling in energy applications.
  • Larger ligand core sizes improved the performance of the complexes, allowing reactions to occur rapidly and efficiently under mild conditions with minimal catalyst use.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!