• 제목/요약/키워드: aqueous chemistry

검색결과 1,704건 처리시간 0.024초

A Simple and One-pot Oxidative Conversion of Alcohols or Aldehydes to the Nitriles using NaIO4/KI in Aqueous NH3

  • Zolfigol, Mohammad Ali;Hajjami, Maryam;Ghorbani-Choghamarani, Arash
    • Bulletin of the Korean Chemical Society
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    • 제32권12호
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    • pp.4191-4194
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    • 2011
  • Sodium periodate ($NaIO_4$) and potassium iodide (KI) in aqueous ammonia has been used for the one-pot synthesis of nitriles from the corresponding aldehydes and alcohols in moderate to good yield. This transformation, proceeds via an in situ oxidation- imination-aldimine oxidation sequence.

Aggregation of Crystal Violet with Tetraphenylborate Anions in Aqueous Solutions

  • Lee, Beom-Gyu;Jung, Rae-Seok;Kim, Kang-Jin
    • Bulletin of the Korean Chemical Society
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    • 제10권2호
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    • pp.148-151
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    • 1989
  • The hydrophobic interaction between tetraphenylborate (TPB$^-$) or tetrakis (4-fluorophenyl)borate (TFB$^-$) and crystal violet has been investigated in aqueous solutions by absorption spectrophotometry. Both of the anions promote the aggregation of the ion pairs formed between crystal violet and TPB$^-$ or TFB$^-$. When crystal violet and borate anion are nearly equimolar, insoluble floating aggregates can be observed. Based on the relative absorbance of H and J bands and on the effect of TX-100, TFB$^-$ is found to be more hydrophobic than TPB$^-$.

Structural and Functional Study of Antimicrobial Peptide Using NMR Spectroscopy

  • Suh, Jeong-Yong;Lee, Young-Tae;Park, Byong-Seok
    • 한국생물물리학회:학술대회논문집
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    • 한국생물물리학회 1997년도 학술발표회
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    • pp.14-14
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    • 1997
  • Structure of potent derivatives of gaegurin, an antimicrobial peptide from Korean frog, is studied by CD and NMR spectroscopy. Gaegurin did not show any secondary structure in aqueous environment, but adopted ${\alpha}$-helix in aqueous TFE solution, SDS and liposome buffer. NMR study showed distinct difference in stability near proline residue in helix.(omitted)

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Study on Thermodynamics of Three Kinds of Benzindocarbocyanine Dyes in Aqueous Methanol Solution

  • Huang, Wei;Wang, Lan-Ying;Fu, Yi-Le;Liu, Ji-Quan;Tao, You-Ni;Fan, Fang-Li;Zhai, Gao-Hong;Wen, Zhen-Yi
    • Bulletin of the Korean Chemical Society
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    • 제30권3호
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    • pp.556-560
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    • 2009
  • Aggregation behavior of three kinds of benzindocarbocyanine dyes in aqueous methanol solution was studied by UV-Vis absorption spectrum. The results indicated that the three dyes all existed monomer-dimer equilibrium in aqueous methanol solution (concentration range $10^{−5}\;to\;10^{−6}$ M) at 25.0$\sim$41.0 ${^{\circ}C}$ for Dye 1, 28.0$\sim$49.0 ${^{\circ}C}$ for Dye 2 and 26.0$\sim$47.0 ${^{\circ}C}$ for Dye 3. The fundamental property of the three dyes as the dimeric association constant KD, the dimeric free energy ${\Delta$}G_D, the dimeric entropy ${\Delta$}S_D, and the dimeric enthalpy ${\Delta$}H_D were determined. The ${\Delta$}H_D of three dyes: Dye 1, Dye 2 and Dye 3 was -42.5, -15.1 and -18.9 kJ/mol, respectively. The experimental observations were the subject of a theoretical study including the ground-state geometries which were fully optimized using DFT at B3LYP/6-31G level. The effect of dye molecule structure on ${\Delta$}H_D was discussed by theoretical calculations.

수용성 미셀용액에서 몇 가지 안트라센 유도체의 가용화 및 감광화 성질 (Solubilization and Photosensitizing Properties of Some Anthracene Derivatives in Aqueous Micellar Solutions)

  • 고정수;한동설;오형식;박병관;김종현;오세웅
    • 대한화학회지
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    • 제35권5호
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    • pp.452-460
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    • 1991
  • 메탄올-물 혼합용매 및 수용성 CTAB, SDS 용액에서 2-에틸안트라센[2-EA]과 9-페닐안트라센[9-PA]에 빛을 조사하는 동안 1,3-디페닐이소벤조푸란[DPBF]이 감소되는 것으로부터 이 반응에 단일항 산소$(^1O_2)$가 관여된다는 화학적 증거를 얻었다. 용매의 극성에 민간함 UV 분광학적 특성을 이용하여 2-EA와 9-PA의 평균미세환경의 극성을 조사하였다. 2-EA와 9-PA가 수용성 CTAB, SDS 및 Brij 35 용액에 가용화될 때 그들의 평균 미세환경은 극성이었으며, 미세환경의 극성 파라미터는 미셀의 이온성에 영향을 받지 않았다. 2-EA의 평균 미세환경의 극성은 40%(w/w) 에탄올 수용액의 극성과 비슷했으며, 9-PA의 경우는 30%(w/w)와 40%(w/w) 사이의 에탄올 수용액의 극성과 비슷했다. 이들 화학종들이 수용성 미셀용액에 가용화될 때 대부분 미셀의 표면에 분포할 것이라는 것을 알았다. 여러 용매에서 2-EA와 9-PA의 광증감능을 검토하였다. 메탄올-물 혼합용매가 수용성 미셀용액보다 광산화반응에 유리한 것으로 나타났다.

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Supramolecular Micelle from Amphiphilic Mn(III)-porphyrin Derivatives as a Potential MRI Contrast Agent

  • Choi, Kwang-Mo;Lee, Do-Hyung;Jang, Woo-Dong
    • Bulletin of the Korean Chemical Society
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    • 제31권3호
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    • pp.639-644
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    • 2010
  • Amphiphilic porphyrin derivatives have been synthesized and characterized by $^1H$ NMR and MALDI-TOF-MS. All porphyrin derivatives showed very high solubility to aqueous medium as well as hydrophobic organic solvent. The UV-vis absorption of the porphyrin derivatives showed significant broadness and decrease of maximum intensity of absorption in aqueous solution. SEM experiment showed the formation of spherical micellar structure. The $T_1$ relaxation time of aqueous medium was drastically decreased in the presence of Mn(III)-porphyrin derivative, indicating that the supramolecular micelle has strong possibility to use as a $T_1$ contrast agent.

Facile and Room Temperature Preparation and Characterization of PbS Nanoparticles in Aqueous [EMIM][EtSO4] Ionic Liquid Using Ultrasonic Irradiation

  • Behboudnia, M.;Habibi-Yangjeh, A.;Jafari-Tarzanag, Y.;Khodayari, A.
    • Bulletin of the Korean Chemical Society
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    • 제30권1호
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    • pp.53-56
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    • 2009
  • At room-temperature, a facile, seedless, and environmentally benign green route for the synthesis of star like PbS nanoclusters at 7 min in aqueous solution of 1-ethyl-3-methylimidazolium ethyl sulfate, [EMIM] [$EtSO_{4}$], room-temperature ionic liquid (RTIL), via ultrasonic irradiation is proposed. The X-ray diffraction studies display that the products are excellently crystallized in the form of cubic structure. An energy dispersive X-ray spectroscopy (EDX) investigation reveals the products are extremely pure. The absorption spectra of the product exhibit band gap energy of about 4.27 eV which shows an enormous blue shift of 3.86 eV that can be attributed to very small size of PbS nanoparticles produced and quantum confinement effect. A possible formation mechanism of the PbS nanoparticles using ultrasonic irradiation in aqueous solution of the RTIL is presented.

Complexes of Polyvalent Metal Ions (Ⅵ). Complexes of Nickel and Cadmium with Dibasic Organic Acids in Aqueous, Ethanol-Water and Acetone-Water Solutions$^*$

  • Sang-Up Choi;Joon-Kil Kang;Young-Il Pae
    • Bulletin of the Korean Chemical Society
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    • 제1권2호
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    • pp.49-54
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    • 1980
  • Solutions of $Ni^{2+}$ and $Cd^{2+}$ were mixed with the solutions of various dibasic organic acids in the presence of cation exchange resin at room temperature. The distribution ratios of the metal ions between resin and solution were measured, using radioactive metal ions as tracer. From the observed variation of the distribution ratios with acid anion concentrations, it was concluded that $Ni^{2+}$ and $Cd^{2+}$ formed one-to-one complexes with succinate, malonate, o-phthalate and tartarate ions in aqueous, 20 % ethanol-water and 20 % acetone-water solutions. The results of the present study indicated that the relative stabilities of the complexes in solution increased generally in the order : $Ni^{2+}$ < $Cd^{2+}$ complexes. Succinate < malonate < o-phthalate < tartarate complexes. Aqueous < mixed solvent systems.

Solubilization of Alcohols in Aqueous Solution of Cetylpyridinium Chloride

  • Chung Jong Jae;Lee Sang Wook;Kim Young Chul
    • Bulletin of the Korean Chemical Society
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    • 제13권6호
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    • pp.647-649
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    • 1992
  • The critical micelle concentration (CMC) values of cetylpyridinium chloride (CPC) in some alcohol-aqueous solutions were determined by UV-Vis spectroscopy at 25$25^{\circ}C$. The CMC of CPC was increased with the addition of methanol and ethanol, while with the addition of propanol it was decreased because of the solubilization of propanol into the micelle of CPC. The ratio (${\beta}$) of the number of counterions to that of surfactant ions associated into micelles in alcohol (methanol, ethanol and propanol) aqueous solutions was measured by using the Shinoda $equation^{17}$. The ratio of counterion binding to the CPC micelles in methanol-and ethanol-water mixtures was larger than in pure water, while the ratio in propanol-water mixture might be much decreased.