| ²é¿´: 1851 | »Ø¸´: 10 | |||
[½»Á÷]
¡¾ÇóÖú¡¿Äø´ß»¯¼ÁµÄÖÆ±¸
|
|||
|
ÇëÎÊһϸ÷λ¸ßÊÖ£¬ÈçºÎÖÆ±¸Ni(dppp)Cl2 1,3-bis(diphenylphosphino)propane]dichloro nickel(¢ò) Ï£ÍûÄÜÌṩÏà¹ØºÏ³ÉÎÄÏ×£¬»¹ÓУ¬ÓÐûÓÐÔÚÖÆ±¸¹ý³ÌÖÐÐèÒªÌØ±ð×¢ÒâµÄµØ·½¡£ ²»Éõ¸Ð¼¤¡£ [ Last edited by jerryak47 on 2010-11-17 at 22:57 ] |
» ²ÂÄãϲ»¶
¹ú¼Ò¼¶È˲ÅÍÅÌå¿ÎÌâ×éÕÐÊÕ2026½ì»¯Ñ§Ààѧ˶£¬×¨Ë¶¡£
ÒѾÓÐ1È˻ظ´
ºÓÄÏÀí¹¤´óѧÂÌÉ«´ß»¯¿ÎÌâ×éÕÐÊÕ²ÄÁÏ£¬»¯¹¤£¬»¯Ñ§µÈ·½ÏòÑо¿Éú
ÒѾÓÐ0È˻ظ´
»¯Ñ§¹¤³Ì¼°¹¤Òµ»¯Ñ§ÂÛÎÄÈóÉ«/·ÒëÔõôÊÕ·Ñ?
ÒѾÓÐ276È˻ظ´
¹ú¼Ò¼¶È˲ſÎÌâ×éÕÐÑо¿Éú £¨´ß»¯·½Ïò£©µ÷¼Á
ÒѾÓÐ13È˻ظ´
ÕÐÊÕ˶ʿÑо¿Éú
ÒѾÓÐ25È˻ظ´
[Ìì½ò]ÖйúÃñº½´óѧ ÕÐÊÕ²ÄÁÏÀàÑо¿Éú
ÒѾÓÐ0È˻ظ´
²ÄÁÏÓ뻯¹¤×¨ÒµÓдóÁ¿µ÷¼ÁÖ¸±ê
ÒѾÓÐ8È˻ظ´
¹ú¼Ò´óÈ˲ſÎÌâ×éÕÐÊÕ»¯Ñ§¡¢²ÄÁÏ»¯¹¤Àà2026Äêµ÷¼ÁÉú
ÒѾÓÐ0È˻ظ´
085600µ÷¼Á
ÒѾÓÐ4È˻ظ´
Õãʦ´ó»¯Óë²ÄѧԺ2026ÄêÓдóÁ¿Ë¶Ê¿Ñо¿Éúµ÷¼ÁÃû¶î £¨ÏßÉÏ µ÷¼Á£©
ÒѾÓÐ7È˻ظ´
¼ªÁÖ¹¤³Ì¼¼Êõʦ·¶Ñ§Ôº ²ÄÁÏÓ뻯¹¤ £¨0856£© ÕÐÊÕµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÕÒÒ»±¾¹ØÓÚ´ß»¯¼ÁÖÆ±¸µÄÊ飬¼±Óã¡£¡£¡£¡£¡°ÑËùÓеĽð±Ò¶¼É¢³öÀ´ÁË
ÒѾÓÐ7È˻ظ´
Äø/Ñõ»¯ÂÁ´ß»¯¼ÁµÄÖÆ±¸¼°ÂÁÄÜ·ñ»¹ÔÄøÑÎ
ÒѾÓÐ9È˻ظ´
ÄòËØ×ö³Áµí¼ÁÖÆ±¸º¬Äø´ß»¯¼Á
ÒѾÓÐ6È˻ظ´
¹ØÓÚNi/¹èÔåÍÁ´ß»¯¼ÁÖÆ±¸µÄÎÊÌâ
ÒѾÓÐ34È˻ظ´
Óйؽþ×Õ·¨ÖƱ¸´ß»¯¼Á¸ºÔØÁ¿µÄÎÊÌâ
ÒѾÓÐ14È˻ظ´
Çó½âÄø»ù´ß»¯¼ÁÖÆ±¸µÄһЩÒÉ»ó
ÒѾÓÐ15È˻ظ´
ÄòËØ³Áµí·¨ÖƱ¸Äø´ß»¯¼Á
ÒѾÓÐ11È˻ظ´
TPDµÄ»¹ÔÌõ¼þÈçºÎÈ·¶¨£¨´ß»¯¼ÁÖÆ±¸²»ÊÇÓÃÇâÆø»¹Ô£©
ÒѾÓÐ8È˻ظ´
Äø´ß»¯¼ÁÖØ¸´ÐÔ²î
ÒѾÓÐ17È˻ظ´
Çë½Ì¹ØÓÚÑõ»¯ÂÁ¸ºÔØÄøîâ½ðÊô´ß»¯¼ÁµÄÖÆ±¸~
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿ÄøÍ¸õ/»îÐÔÌ¿´ß»¯¼ÁÖÆ±¸
ÒѾÓÐ17È˻ظ´
¡¾ÇóÖú¡¿¸ºÔØÐÍÄø»ù´ß»¯¼ÁÓÃÇáÇâÆø»î»¯»¹ÔµÄÎÊÌâ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿Äø-²¬Ë«½ðÊô´ß»¯¼ÁµÄÖÆ±¸ÎÊÌâ
ÒѾÓÐ4È˻ظ´
» ÇÀ½ð±ÒÀ²£¡»ØÌû¾Í¿ÉÒԵõ½:
î÷Îý»¯ºÏÎï°ëµ¼Ìå²ÄÁÏÓëÆ÷¼þÍŶÓ[ÍÆ½é]
+3/148
¡¾µ÷¼ÁÐÅÏ¢¡¿É½¶«¿Æ¼¼´óѧ£¨ÇàµºÐ£Çø£©²ÄÁÏÖú¼ÁÑо¿ÍŶÓÕÐÊÕµ÷¼Á˶ʿÑо¿Éú
+1/90
°²»ÕËÞÖÝѧԺ085600²ÄÁÏÓ뻯¹¤(רҵѧλ)2026ÄêÑо¿ÉúÕÐÉúµ÷¼ÁÐÅÏ¢
+1/88
Î人´óѧÓëÕã½Ê¦·¶´óѧ/Î人¹¤³Ì´óѧÁªºÏÅàÑøË¶Ê¿Ñо¿Éúµ÷¼ÁÕÐÉú
+1/88
ÐìÖÝÒ½¿Æ´óѧ ÉúÎïҽѧ¹¤³Ì ѧ˶/ר˶ ½ÓÊÜ-ÉúÎҽѧ¡¢²ÄÁÏ¡¢»¯Ñ§Ïà¹Ø×¨Òµ-µ÷¼ÁÉêÇë
+2/80
ºÓ±±´óѧÎÞ»ú»¯Ñ§×¨ÒµÕÐÊÕµ÷¼ÁÉú
+1/40
Î÷°²¹¤³Ì´óѧ²ÄÁÏѧԺÑî½Ü¿ÎÌâ×éÕÐÊÕ¿¼Ñе÷¼ÁÉú
+1/38
ÖÐɽ´óѧÅËÔ½½ÌÊÚÏÖÐÂÔö1¸ö·Ö×ÓҽѧѧÊõѧλ˶ʿÃû¶î
+1/35
»¶ÓÉúÎïҽѧ¹¤³Ì¡¢Ò©Ñ§¡¢ÉúÎï¡¢Ò±½ð¡¢¼ÆËã»úµÈ×ۺϱíÏÖÓÅÐãͬѧ¿çµ÷-ÉϺ£
+1/31
´óÁ¬¹¤Òµ´óѧ ¸ß·Ö×Ó²ÄÁÏ ½ÓÊÕ¿¼Ñе÷¼Á
+1/18
Çà¿Æ´ó½ÓÊÕ²ÄÁÏÀà¡¢»¯¹¤»¯Ñ§Ààµ÷¼ÁÑо¿Éú£¨Ð뿼Êýѧ£©
+1/18
ÇàÄ곤½Ñ§ÕßÍÅ¶Ó 2026Äê ˶ʿÑо¿Éú ÕÐÊÕµ÷¼Á¿¼Éú
+1/10
Î人·ÄÖ¯´óѧÕÐÊÕ»¯Ñ§»¯¹¤ÀàºÍ²ÄÁÏÀàÑо¿Éúµ÷¼ÁÉúÈô¸ÉÃû
+1/9
º£ÄÏ´óѧ»¯Ñ§Ôº¡ª¹¦ÄÜ·Ö×ÓÆ÷¼þÍŶÓ2026²©Ê¿/Ñо¿ÖúÀíÕÐÉú+²©Ê¿ºóÕÐÆ¸
+1/8
ÖйúÁÖ¿ÆÔºÄ¾²ÄËù˶ʿµ÷¼Á
+1/6
2026ÄêÎ÷»ª´óѧ²ÄÁÏѧԺ-²ÄÁϽü¾»³ÉÐÎÓë±íÃæ¼¼ÊõÑо¿ÍŶÓ-ÕÐÊÕµ÷¼ÁÑо¿Éú
+1/6
Æë³¹¤Òµ´óѧ£¨É½¶«Ê¡¿ÆÑ§Ôº£© ¹ÈÑÇÍþÀÏʦ¿ÎÌâ×éÄâÕÐ2026Äêµ÷¼ÁÑо¿Éú
+1/5
¸ÓÄÏʦ·¶´óѧ¹ùά¿ÎÌâ×éÕÐÊÕ»¯Ñ§ÀࡢҩѧÀà¡¢²ÄÁÏÀàѧ˶¡¢×¨Ë¶¿¼Ñе÷¼Áͬѧ
+1/3
н®´óѧ »¯Ñ§×¨Òµ ˶ʿÑо¿Éúµ÷¼ÁÐÅÏ¢
+1/3
±±¾©¸ßУ¸±Ð£³¤ÍŶÓÕÐÊÕ»úеÀ࣬»·¾³Ààѧ˶ºÍר˶
+1/1
2Â¥2010-11-18 09:55:36
3Â¥2010-11-18 18:31:59
¡ï ¡ï
jerryak47(½ð±Ò+2):лл²ÎÓë
jinkai838(½ð±Ò+1):лл1 2010-11-19 00:06:44
jerryak47(½ð±Ò+2):лл²ÎÓë
jinkai838(½ð±Ò+1):лл1 2010-11-19 00:06:44
|
¹ºÂò ²»ÊÇÌ«¹ó°¡£¬Ëµ²»¶¨ºÏ³É³É±¾Ò²Õâ¸ö¼Û¸ñ http://www.chemicalbook.com/Chem ... ty_CN_CB3416370.htm ¡® wiki ÖоÍÓа¡ £¬http://en.wikipedia.org/wiki/Dic ... hino)propane)nickel ÀïÃæµÄµÚһƪÎÄÏס£ Preparation NiCl2(dppp) is prepared by combining equal molar portions of nickel(II) chloride hexahydrate with 1,3-bis(diphenylphosphino)propane in 2-propanol.[1] Ni(H2O)6Cl2 + dppp ¡ú NiCl2(dppp) + 6 H2O [edit]Reactions It is used in Grignard reagent reactions involving cross-coupling of aryl halides, converting enol ethers, dithioacetals, and vinyl sulfides to olefins. NiCl2(dppp) is used because the douple phosphate ligand minimizes the reduction reactions with labile ¦Â-hydrogens. [2] Cross-coupling reactions of R-X compounds with organometallic nucleophiles are catalyzed by transition metal complexes such as NiCl2(dppp). The R group consists of aryl, vinyl, or allyl groups and the X group is a good leaving group. Cross-coupling reactions are effective at producing carbon-carbon bonds. Catalysts that have bidentate phosphine ligands serve as the best catalysts.[3] NiCl2(dppp) serves as the catalyst by bonding the two cross-coupling components to the nickel. The cross-coupling proceeds by oxidative addition of the aryl, vinyl, or allyl halide to NiCl2(dppp) forming an oxidative addition adduct, R1-NiCl(dppp). The organometallic nucleophile, R2-MgBr, reacts with R1-NiCl(dppp) and is followed by the cross-coupling reaction producing the R1-R2 product. [4] The compound is a catalyst for Kumada coupling reactions involving alkyl, alkenyl, aryl, and heteroaryl Grignard reagents with aryl, heteroaryl, and alkenyl halides. [1] [edit]References ^ a b Kumada, Makota; Tamao, Kohei; Sumitani, Koji (1988), "Phosphine-Nickel Complex Catalyzed Cross-Coupling of Grignard Reagents with Aryl and Alkenyl Halides: 1,2-dibutylbenzene", Org. Synth.; Coll. Vol. 6: 407 |
4Â¥2010-11-18 18:58:16
5Â¥2010-11-18 20:50:43
6Â¥2010-11-19 09:10:29
10Â¥2012-09-01 16:33:52
11Â¥2015-01-26 21:55:11
¼òµ¥»Ø¸´
kuixing7Â¥
2012-08-27 08:47
»Ø¸´
jerryak47(½ð±Ò+2): лл²ÎÓë


kuixing8Â¥
2012-08-27 08:48
»Ø¸´
jerryak47(½ð±Ò+2): лл²ÎÓë

kuixing9Â¥
2012-08-27 08:48
»Ø¸´
jerryak47(½ð±Ò+2): лл²ÎÓë















»Ø¸´´ËÂ¥
Õâ¸ö¿´²»Ì«¶®£¬²»ÊÇÂÈ»¯Äø°É£¬ºÃ¸´ÔÓѽ
£¬¿É·ñ¸ø¸öººÓïÃû×Ö£¬²»ÊìϤ¡£¡£¡£