Language:
English
繁體中文
Help
回圖書館首頁
手機版館藏查詢
Login
Back
Switch To:
Labeled
|
MARC Mode
|
ISBD
Elastomeric polypropylene from unbri...
~
Wilmes, Gregg Michael.
Linked to FindBook
Google Book
Amazon
博客來
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation.
Record Type:
Electronic resources : Monograph/item
Title/Author:
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation./
Author:
Wilmes, Gregg Michael.
Description:
161 p.
Notes:
Source: Dissertation Abstracts International, Volume: 64-11, Section: B, page: 5551.
Contained By:
Dissertation Abstracts International64-11B.
Subject:
Chemistry, Polymer. -
Online resource:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3111823
ISBN:
0496593536
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation.
Wilmes, Gregg Michael.
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation.
- 161 p.
Source: Dissertation Abstracts International, Volume: 64-11, Section: B, page: 5551.
Thesis (Ph.D.)--Stanford University, 2004.
Unbridged group 4 bis(2-arylindenyl)metallocenes are active catalysts for the formation of elastomeric stereoblock polypropylene when activated by a cocatalyst, typically methylaluminoxane (MAO). Careful mechanistic studies of these catalyst systems are compromised by the ill-defined nature of MAO. Well-defined stoichiometric cocatalysts leading to boron-based counteranions have here been used for polymerization and NMR studies.
ISBN: 0496593536Subjects--Topical Terms:
1018428
Chemistry, Polymer.
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation.
LDR
:03841nmm 2200325 4500
001
1844107
005
20051017073434.5
008
130614s2004 eng d
020
$a
0496593536
035
$a
(UnM)AAI3111823
035
$a
AAI3111823
040
$a
UnM
$c
UnM
100
1
$a
Wilmes, Gregg Michael.
$3
1932310
245
1 0
$a
Elastomeric polypropylene from unbridged bis(2-arylindenyl) metallocenes: Investigation of the mechanism of stereoblock polypropylene formation.
300
$a
161 p.
500
$a
Source: Dissertation Abstracts International, Volume: 64-11, Section: B, page: 5551.
500
$a
Adviser: Robert M. Waymouth.
502
$a
Thesis (Ph.D.)--Stanford University, 2004.
520
$a
Unbridged group 4 bis(2-arylindenyl)metallocenes are active catalysts for the formation of elastomeric stereoblock polypropylene when activated by a cocatalyst, typically methylaluminoxane (MAO). Careful mechanistic studies of these catalyst systems are compromised by the ill-defined nature of MAO. Well-defined stoichiometric cocatalysts leading to boron-based counteranions have here been used for polymerization and NMR studies.
520
$a
Propylene polymerizations in liquid propylene by bis(2-phenylindenyl)zirconium dimethyl activated by MAO, trityl tetrakis(pentafluorophenyl)borate, dimethylanilinium tetrakis(pentafluorophenyl)borate, or tris(pentafluorophenyl)borane (B(C 6F5)3) revealed a significant influence of cocatalyst on the polymerization behavior of these catalysts. The productivity and stereoselectivity of the catalyst systems were highest with MAO and lowest with B(C6F 5)3, with B(C6F5)3 yielding amorphous atactic polypropylenes. The presence of aluminum isobutyl groups, either on MAO or from added triisobutylaluminum, increased the stereoselectivity of the polymerizations; the polarity had little influence on the stereoselectivity.
520
$a
The sterically hindered metallocene bis(2-(3,5-di-tert-butylphenyl)indenyl)zirconium dichloride produced polypropylenes of much higher isotacticity than did bis(2-phenylindenyl)zirconium dichloride. Lower-tacticity polypropylenes generated with the sterically hindered compound contained a high percentage of [mmrm] stereoerrors, indicative of a stereoblock microstructure comprised of isotactic stereosequences of opposite relative configuration. Bis(2-(3,5-di-tert-butylphenyl)indenyl)hafnium dichloride produced polypropylenes of moderate tacticity and did not show a drop in productivity or stereocontrol with increasing temperature.
520
$a
A series of unbridged bis(2-arylindenyl)zirconocenes varying both in the pi indenyl ligand framework and the sigma ligand was synthesized. The rotation rates of the dimethyl-substituted metallocenes were too fast to be determined by standard NMR techniques. On-resonance spin lattice relaxation in the rotating frame (T1rho) was used to determine the rate of rotation of the aryl ligands in the dimethyl species. The nature of both the sigma and the pi ligand systems affects the rate with sterically bulky substituents resulting in slower rotation. The effect of the sigma ligand is substantially stronger than that of the pi ligand.
520
$a
Variable temperature NMR studies of bis(2-arylindenyl)zirconium dimethyl compounds activated by B(C6F5)3 showed dynamic behavior consistent with fast ligand rotation and slower rearrangement of the ion pairs. Model compounds of the cationic active species were synthesized, and the conformation of the pi-ligand framework could be influenced to give a Cs-symmetric syn isomer of the metallocene.
590
$a
School code: 0212.
650
4
$a
Chemistry, Polymer.
$3
1018428
650
4
$a
Chemistry, Inorganic.
$3
517253
690
$a
0495
690
$a
0488
710
2 0
$a
Stanford University.
$3
754827
773
0
$t
Dissertation Abstracts International
$g
64-11B.
790
1 0
$a
Waymouth, Robert M.,
$e
advisor
790
$a
0212
791
$a
Ph.D.
792
$a
2004
856
4 0
$u
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3111823
based on 0 review(s)
Location:
ALL
電子資源
Year:
Volume Number:
Items
1 records • Pages 1 •
1
Inventory Number
Location Name
Item Class
Material type
Call number
Usage Class
Loan Status
No. of reservations
Opac note
Attachments
W9193621
電子資源
11.線上閱覽_V
電子書
EB
一般使用(Normal)
On shelf
0
1 records • Pages 1 •
1
Multimedia
Reviews
Add a review
and share your thoughts with other readers
Export
pickup library
Processing
...
Change password
Login