Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group

Sheng Di Bai; Jian Ping Guo; Dian Sheng Liu; Wai Yeung Wong

doi:10.1002/ejic.200600658

Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group

Sheng Di Bai, Jian Ping Guo, Dian Sheng Liu, Wai Yeung Wong

Research output: Journal article publication › Journal article › Academic research › peer-review

22 Citations (Scopus)

Abstract

A novel class of silyl-linked bis(amidinate) ligands [SiMe2-{NC(Ph)N(2,6-R2Ph)Li)2] [L1(R = H), L2(R = Me), and L3(R = iPr)] reacted with TiCl3(C5H5) to produce the half-sandwich titanium complexes 1,2, and 3. The molecular structures of 1-3 were confirmed successfully by X-ray crystallography. An unprecedented intramolecular ligand transformation from the linked bis(amidinate) configuration to the linked imido-amidinate configuration took place in the cases of L1and L2. It was found that the rearrangement process was related to the steric hindrance of the terminal substituents. KGaA, 2006.

Original language	English
Pages (from-to)	4903-4907
Number of pages	5
Journal	European Journal of Inorganic Chemistry
Issue number	23
DOIs	https://doi.org/10.1002/ejic.200600658
Publication status	Published - 4 Dec 2006
Externally published	Yes

Keywords

Bis(amidinate)
Bulky hindrance
Crystal structure
Ligand transformation
Steric hindrance
Titanium

ASJC Scopus subject areas

Inorganic Chemistry

More information

10.1002/ejic.200600658

Cite this

@article{932493c4389c4fcb93dd712d248487eb,

title = "Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group",

abstract = "A novel class of silyl-linked bis(amidinate) ligands [SiMe2-\{NC(Ph)N(2,6-R2Ph)Li)2] [L1(R = H), L2(R = Me), and L3(R = iPr)] reacted with TiCl3(C5H5) to produce the half-sandwich titanium complexes 1,2, and 3. The molecular structures of 1-3 were confirmed successfully by X-ray crystallography. An unprecedented intramolecular ligand transformation from the linked bis(amidinate) configuration to the linked imido-amidinate configuration took place in the cases of L1and L2. It was found that the rearrangement process was related to the steric hindrance of the terminal substituents. KGaA, 2006.",

keywords = "Bis(amidinate), Bulky hindrance, Crystal structure, Ligand transformation, Steric hindrance, Titanium",

author = "Bai, \{Sheng Di\} and Guo, \{Jian Ping\} and Liu, \{Dian Sheng\} and Wong, \{Wai Yeung\}",

year = "2006",

month = dec,

day = "4",

doi = "10.1002/ejic.200600658",

language = "English",

pages = "4903--4907",

journal = "European Journal of Inorganic Chemistry",

issn = "1434-1948",

publisher = "Wiley-VCH Verlag",

number = "23",

}

Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group. / Bai, Sheng Di; Guo, Jian Ping; Liu, Dian Sheng et al.
In: European Journal of Inorganic Chemistry, No. 23, 04.12.2006, p. 4903-4907.

Research output: Journal article publication › Journal article › Academic research › peer-review

TY - JOUR

T1 - Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group

AU - Bai, Sheng Di

AU - Guo, Jian Ping

AU - Liu, Dian Sheng

AU - Wong, Wai Yeung

PY - 2006/12/4

Y1 - 2006/12/4

N2 - A novel class of silyl-linked bis(amidinate) ligands [SiMe2-{NC(Ph)N(2,6-R2Ph)Li)2] [L1(R = H), L2(R = Me), and L3(R = iPr)] reacted with TiCl3(C5H5) to produce the half-sandwich titanium complexes 1,2, and 3. The molecular structures of 1-3 were confirmed successfully by X-ray crystallography. An unprecedented intramolecular ligand transformation from the linked bis(amidinate) configuration to the linked imido-amidinate configuration took place in the cases of L1and L2. It was found that the rearrangement process was related to the steric hindrance of the terminal substituents. KGaA, 2006.

AB - A novel class of silyl-linked bis(amidinate) ligands [SiMe2-{NC(Ph)N(2,6-R2Ph)Li)2] [L1(R = H), L2(R = Me), and L3(R = iPr)] reacted with TiCl3(C5H5) to produce the half-sandwich titanium complexes 1,2, and 3. The molecular structures of 1-3 were confirmed successfully by X-ray crystallography. An unprecedented intramolecular ligand transformation from the linked bis(amidinate) configuration to the linked imido-amidinate configuration took place in the cases of L1and L2. It was found that the rearrangement process was related to the steric hindrance of the terminal substituents. KGaA, 2006.

KW - Bis(amidinate)

KW - Bulky hindrance

KW - Crystal structure

KW - Ligand transformation

KW - Steric hindrance

KW - Titanium

UR - https://www.scopus.com/pages/publications/33845666616

U2 - 10.1002/ejic.200600658

DO - 10.1002/ejic.200600658

M3 - Journal article

SN - 1434-1948

SP - 4903

EP - 4907

JO - European Journal of Inorganic Chemistry

JF - European Journal of Inorganic Chemistry

IS - 23

ER -

Bulky-hindrance-controlled ligand transformation from linked bis(amidinate) to linked imido-amidinate promoted by a mono(cyclopentadienyl)titanium group

Abstract

Keywords

ASJC Scopus subject areas

More information

Other files and links

Fingerprint

Cite this