• Macromolecular Research
• /
• 제14권5호
• /
• pp.539-544
• /
• 2006

2-Furancarboxaldehyde-2-pyridinylhydrazone (FPH) and 5-methyl-2-furancarboxaldehyde-2-pyridinylhydrazone (MFPH) were synthesized and used as tridentate ligands of copper (I) bromide for the atom transfer radical polymerization of methyl methacrylate (MMA) and styrene. The polymerization of methyl methacrylate achieved high conversion and yielded polymers with a good control of molecular weight and low polydispersity (PDI=1.33). Higher PDI were observed in the polymerization of styrene. Using 1-phenyl ethylbromide (PEBr) and ethyl 2-bromoisobutyrate (EBiB) as model compounds for the polymeric chain ends, the activation rate constants of the new catalytic systems were measured. These results were correlated with the polymerization results and compared with another catalytic system previously reported.

• Bulletin of the Korean Chemical Society
• /
• 제21권1호
• /
• pp.65-68
• /
• 2000

A $\mu-oxo$ diiron(III) complex and two bis( $\mu-alkoxo)$ diiron(III) complexes with biomimetic tripodal ligand containing mixed N/O donor atoms were synthesized using a mononuclear iron(III) complex as starting material. Depending on the amounts and kinds of bases used, we obtained various kinds of diiron (III) complexes. The reaction of $[$Fe^{III}$(Hbbea)Cl_2]Cl$, 1, with an equivalent amount of $KO_2$ or NaOAc produced $[$Fe^{III}$_2O(Hb-bea)_2Cl_2]Cl_2$, 2. An additional equivalent amount of NaOBz or NaOAc converts complex 2 to complex 3 or complex 4 depending on the base used. The addition of two equivalent amounts of NaOBz orNaOAc directly converts complex 1 to $[$Fe^{III}$_2(bbea)_2(OBz)_2]Cl_2$, 3, or $[$Fe^{III}$_2(bbea)_2(OAc)_2]Cl_2$, 4, depending on the base used. Crystal data are as follows: [$Fe^{III}_2O(Hbbea)_2Cl_2]Cl_2$, 2: monoclinic space group $$P2_1/n$$, a = 8.421 (1) $\AA$, b = 18.416 (2) $\AA$, c = 13.736 (1) $\AA$, $\beta$ = 104.870 $(7)^{\circ}$, V = 2058.9 (4) $\AA^3$, Z = 2, R1 = 0.0469 and wR2 = 0.1201 for reflections with I > 2 ${\sigma}$(I).

• 분석과학
• /
• 제7권2호
• /
• pp.225-232
• /
• 1994

$Pb^{2+}$에 대해 $Ag^+$의 높은 추출 선택성이 기대되는 비고리 폴리에테르인 포단드 I-VII을 설계하여 높은 수율로 합성하였다. 포단드 I-VII을 추출제로 이용하여 물/클로로포름계에서 $Ag^+$ 및 $Pb^{2+}$의 피크린산염에 대한 %추출률(%Ex)을 구하였다. 또한 $Ag^+$과 포단드 I-VII과의 착물 형성에 대한 안전도상수(log K)를 전위차 적정에 의해 구하였다. %Ex($Ag^+$)는 치환된 황주개원자 수에 비례하였으나, 황 주개원자가 3개 치환된 포단드 VI(log K:7.65)와 4개 치환된 포단드 VII(log K:9.15)은 모두 100%에 가까운 추출률을 나타내었다. %Ex($Ag^+/Pb^{2+}$)에 있어서는 산소-황 혼합주개 포단드(IV-VII)가 더 큰 값을 나타내었다. 한편, %Ex($Ag^+$) 및 log K의 크기는 황주개자리의 변화에 크게 의존하였는데, 이는 NMR 실험결과 방향족 말단기 사이의 ${\pi}-{\pi}$ 스텍킹 상호작용에 기인한 것으로 생각된다.