홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Octanoic acid, nickel(2+) salt (2:1) → HCID 22229092, 화합물

HRID 1744393
노트
인쇄 미리보기

반응식

HRID 1744393 반응식
C([O-])(=O)CCCCCCC.[Ni+2:11].C([O-])(=O)CCCCCCC.[F:22][Sb-:23]([F:28])([F:27])([F:26])([F:25])[F:24].[H+]>CCCCCC>[F:22][Sb-:23]([F:28])([F:27])([F:26])([F:25])[F:24].[F:22][Sb-:23]([F:28])([F:27])([F:26])([F:25])[F:24].[Ni+2:11]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 168988Octanoic acid, nickel(2+) salt (2:1)HCID 21953576Hydrogen hexafluoridoantimonate(1-)

생성물 1

HCID 22229092HCID 22229092, 화합물

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

A hexane solution of nickel octanoate was reacted with hexafluoroantimonic acid at −10° C. at a molar ratio of 1:1, and a precipitate of nickel bis(hexafluoroantimonate) [Ni(SbF6)2] formed as a by-product was removed by filtration. The resulting product was diluted with toluene. A reaction vessel was charged with 0.40 mmol (as a nickel atom) of the resulting hexafluoroantimonic acid-modified product of nickel octanoate, 1.2 mmol of boron trifluoride ethyl etherate, 8.0 mmol of methylalumoxane, 0.4 mmol of 1,5-cyclooctadiene and 8.0 mmol of methyltriethoxysilane in the order of methyltriethoxysilane, 1,5-cyclooctadiene, methylalumoxane, boron trifluoride ethyl etherate and the hexafluoroantimonic acid-modified product of nickel octanoate, and polymerization was initiated. The polymerization was conducted at 30° C. for 3 hours, and methanol was added to terminate the polymerization. The conversion rate of the monomers to the copolymer was 73%.

출처 및 근거

ORD 기록
ord-6f16102884864d43bfcf3d2f8bb7d65a
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07015293B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트