Synthesis and X-ray crystal structures of [Ph2PMe2] [(η5-C5H4But)2Li] and [(n5-C5H4But)2Yb(Cl)Ch2P(Me)Ph2]

Wai Kwok Wong; Lilu Zhang; Wing Tak Wong; Feng Xue; Thomas C.W. Mak

doi:10.1016/0277-5387(96)00231-8

Synthesis and X-ray crystal structures of [Ph₂PMe₂] [(η⁵-C₅H₄Bu^t)₂Li] and [(n⁵-C₅H₄Bu^t)₂Yb(Cl)Ch₂P(Me)Ph₂]

Wai Kwok Wong
, Lilu Zhang
, Wing Tak Wong
, Feng Xue
, Thomas C.W. Mak

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

13 Citations (Scopus)

Abstract

The interaction of [(η5-C5H4But)2YbCl · LiCl] with one equivalent of Li[(CH2) (CH2)PPh2] in tetrahydrofuran gave [Ph2PMe2] [(η5-C5H4But)2Li] (1) and [(η5-C5H4But)2Yb(Cl)CH2P(Me)Ph2] (2) in 10% and 30% yields, respectively. 1 could also be prepared in 70% yield from the reaction of [Ph2PMe2][CF3SO3] with two equivalents of (C5H4But)Li. Both compounds have been fully characterized by analytical, spectroscopic and X-ray diffraction methods. The solid state structure of 1 reveals a sandwich structure for the [(η5-C5H4But)2Li]-anion.

Original language	English
Pages (from-to)	4593-4597
Number of pages	5
Journal	Polyhedron
Volume	15
Issue number	24
DOIs	https://doi.org/10.1016/0277-5387(96)00231-8
Publication status	Published - 13 Sept 1996
Externally published	Yes

ASJC Scopus subject areas

Physical and Theoretical Chemistry
Inorganic Chemistry
Materials Chemistry

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10.1016/0277-5387(96)00231-8

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@article{807b45a4c29a455cac9e76c4e4cddfe0,

title = "Synthesis and X-ray crystal structures of [Ph2PMe2] [(η5-C5H4But)2Li] and [(n5-C5H4But)2Yb(Cl)Ch2P(Me)Ph2]",

abstract = "The interaction of [(η5-C5H4But)2YbCl · LiCl] with one equivalent of Li[(CH2) (CH2)PPh2] in tetrahydrofuran gave [Ph2PMe2] [(η5-C5H4But)2Li] (1) and [(η5-C5H4But)2Yb(Cl)CH2P(Me)Ph2] (2) in 10\% and 30\% yields, respectively. 1 could also be prepared in 70\% yield from the reaction of [Ph2PMe2][CF3SO3] with two equivalents of (C5H4But)Li. Both compounds have been fully characterized by analytical, spectroscopic and X-ray diffraction methods. The solid state structure of 1 reveals a sandwich structure for the [(η5-C5H4But)2Li]-anion.",

author = "Wong, \{Wai Kwok\} and Lilu Zhang and Wong, \{Wing Tak\} and Feng Xue and Mak, \{Thomas C.W.\}",

year = "1996",

month = sep,

day = "13",

doi = "10.1016/0277-5387(96)00231-8",

language = "English",

volume = "15",

pages = "4593--4597",

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TY - JOUR

T1 - Synthesis and X-ray crystal structures of [Ph2PMe2] [(η5-C5H4But)2Li] and [(n5-C5H4But)2Yb(Cl)Ch2P(Me)Ph2]

AU - Wong, Wai Kwok

AU - Zhang, Lilu

AU - Wong, Wing Tak

AU - Xue, Feng

AU - Mak, Thomas C.W.

PY - 1996/9/13

Y1 - 1996/9/13

N2 - The interaction of [(η5-C5H4But)2YbCl · LiCl] with one equivalent of Li[(CH2) (CH2)PPh2] in tetrahydrofuran gave [Ph2PMe2] [(η5-C5H4But)2Li] (1) and [(η5-C5H4But)2Yb(Cl)CH2P(Me)Ph2] (2) in 10% and 30% yields, respectively. 1 could also be prepared in 70% yield from the reaction of [Ph2PMe2][CF3SO3] with two equivalents of (C5H4But)Li. Both compounds have been fully characterized by analytical, spectroscopic and X-ray diffraction methods. The solid state structure of 1 reveals a sandwich structure for the [(η5-C5H4But)2Li]-anion.

AB - The interaction of [(η5-C5H4But)2YbCl · LiCl] with one equivalent of Li[(CH2) (CH2)PPh2] in tetrahydrofuran gave [Ph2PMe2] [(η5-C5H4But)2Li] (1) and [(η5-C5H4But)2Yb(Cl)CH2P(Me)Ph2] (2) in 10% and 30% yields, respectively. 1 could also be prepared in 70% yield from the reaction of [Ph2PMe2][CF3SO3] with two equivalents of (C5H4But)Li. Both compounds have been fully characterized by analytical, spectroscopic and X-ray diffraction methods. The solid state structure of 1 reveals a sandwich structure for the [(η5-C5H4But)2Li]-anion.

UR - https://www.scopus.com/pages/publications/0001321637

U2 - 10.1016/0277-5387(96)00231-8

DO - 10.1016/0277-5387(96)00231-8

M3 - Journal article

SN - 0277-5387

VL - 15

SP - 4593

EP - 4597

JO - Polyhedron

JF - Polyhedron

IS - 24

ER -

Synthesis and X-ray crystal structures of [Ph₂PMe₂] [(η⁵-C₅H₄Bu^t)₂Li] and [(n⁵-C₅H₄Bu^t)₂Yb(Cl)Ch₂P(Me)Ph₂]

Abstract

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