2002
DOI: 10.1007/bf02699307
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Olefin homopolymerization catalyzed over asymmetric and symmetric ni(II) diimine complexes

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Cited by 4 publications
(3 citation statements)
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“…Ethyl groups have a lower stereo volume than isopropyl groups and then it is possible to observe that complex that leaves the most exposed nickel atom produces polymers with a higher crystalline fraction, while bulkier substituents provide greater ease of transfer reactions. Moreover, the higher steric hindrance the more difficult the chain termination by associative displacement transfer (Hβ) [23].…”
Section: Influence Of the Complex Structure On The Ethylene Polymerizmentioning
confidence: 99%
“…Ethyl groups have a lower stereo volume than isopropyl groups and then it is possible to observe that complex that leaves the most exposed nickel atom produces polymers with a higher crystalline fraction, while bulkier substituents provide greater ease of transfer reactions. Moreover, the higher steric hindrance the more difficult the chain termination by associative displacement transfer (Hβ) [23].…”
Section: Influence Of the Complex Structure On The Ethylene Polymerizmentioning
confidence: 99%
“…~³ molecular sieve adsorption öro Ê @@Ñ M« s Wz Q-OÇ Ê ôfõ «ÄGñ ~-GÊÉ G2 í Hê π-comlexation Yk³ >J ~-õ «ÄG2 ör«. c³ X, Y zeolite÷ polystyrenes @@³ ÄGñ ñ,Ñ M « s WzQ-OÇ Ê ôfõ «ÄK [9,10]. .~³ absorptions «ÄK öro propionitrile«÷ p-xylene Ùê ço Ä kÑ M« ¯ C-2 o dYís ÄgQ-OÇ ÄUs «ÄGñ ethylene/ethane, propylene/propane Ùs ~-G2) «Ä K [9,11].…”
Section: «unclassified
“…ͤ, HNO 3 Ù MJ 9Ss <4Ý2 Y× s ¤}G. {ê ç« 4Í@ AEQs ¡¤³ Gñ Y×s D} G. ~2 pyridine P 9S ¡d, .~2 H P 9S ¡ d, »~2 ͤ P 9S ¡d, K@Lk³ copper powderQ cuprous nitrate trihydrate P 9S ¡d Ùs g MJ õ 2 Y×s ¤}G. Cu(0)ê Cu(II)õ äQE Cu(I)õ G, .g2 ligand³ pyridine« 1®G[10,15]. «6K pyridines ¬O ñ…”
unclassified