• 제목/요약/키워드: Photoinduced electron-transfer

검색결과 41건 처리시간 0.021초

Noncovalently Linked Zinc Porphyrin-Ru(bpy)3 Dyad Assembled via Axial Coordination

  • Kim, Dol;Shin, Eun-Ju
    • Bulletin of the Korean Chemical Society
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    • 제24권10호
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    • pp.1490-1494
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    • 2003
  • Noncovalently linked electron donor-acceptor dyad consisting of zinc tetratolylporphyrin and pyridine appended ruthenium trisbipyridine comlex was prepared, via axial coordination of pyridine moiety in ruthenium trisbipyridine complex on zinc tetratolylporphyrin. For the purpose of comparison, axial coordination of pyridine-appended 2,2'-bipyridine on zinc tetratolylporphyrin was also investigated. The Kvalues were detemined based on absorption of fluorescence studies. The fluorescence of zinc teratolylporphrin was efficiently quenched upon axial coordination of pyridine moiety, prbably due to the photoinduced electron transfer from zinc tetrtolylporphyrin to ruthenium trisbipyridine, supported by free enegy estimation.

Solvatochromism, Aggregation and Photochemical Properties of Fullerenes, $C_{60} and C_{70}$, in Solution

  • Nath, Sukhendu;Pal, Haridas;Sapre, Avinash.V.;Mittal, Jai.P.
    • Journal of Photoscience
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    • 제10권1호
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    • pp.105-119
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    • 2003
  • Fullerenes, $C_{60}$ and $C_{70}$, display interesting physicochemical properties in solutions, especially due to their unique chemical structures and their good electron accepting abilities. Solubility of fullerenes in different organic solvents and their unusual solvatochromic behavior, the ability of the fullerenes to form aggregates in solutions, and their electron transfer and charge transfer interactions with variety of electron donors, are the subjects of extensive research activities for more than one decade. Many research groups including ours have contributed substantially in the understanding of the solvatochromism, aggregation behavior, and the photoinduced electron transfer and charge transfer chemistry of fullerenes, in condensed phase. Present article is aimed to summarize the important results reported on the above aspects of fullerenes, subsequent to the earlier report from our group (D.K. Palit and J.P. Mittal, Full. Sci. & Tech. 3, 1995, 643-659).)., 643-659)..

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An off-on Fluorescent Sensor for Detecting a Wide Range of Water Content in Organic Solvents

  • Kim, Kang-Hyeon;Lee, Wan-Jin;Kim, Jae Nyoung;Kim, Hyung Jin
    • Bulletin of the Korean Chemical Society
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    • 제34권8호
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    • pp.2261-2266
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    • 2013
  • This paper describes the synthesis and water sensing properties of a fluorescent photoinduced electron transfer (PET) sensor (5) with an extended operating sensing range. The 1,8-naphthalimide derivative (5) attached with a piperazine group and a carboxylic group was synthesized and applied as a fluorescent water sensor in water-miscible organic solvents. The fluorescence intensity of the dye 5 increased with increasing water content up to 80% (v/v) and the fluorescence intensities were enhanced 45-, 67- and 122-fold in aqueous EtOH, DMF and DMSO solutions, respectively. In aqueous acetone solution, the enhancement of the fluorescence intensities was somewhat lower (30-fold) but the response range was wider (0-90%, v/v).

Ketyl radical formation of excited 1, 8-naphthalimides in protic polar solvent

  • Cho, Dae Won;Cho, Dae Won;Park, Hea Jung;Yoon, Ung Chan;Lee, Myoung Hee;Im, Chan
    • Rapid Communication in Photoscience
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    • 제1권2호
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    • pp.35-37
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    • 2012
  • Photoinduced electron-transfer process of 1,8-naphthalimide-linker-trimethylsilane (NI-O3-TMS, O3 = 3,6,9-trioxaundecyl) and NI-O3 has been investigated using the transient absorption measurements in $CH_3CN$ and $CH_3CN/H_2O$. The excitation of NI-O3-TMS in $CH_3CN$ produced the NI radical anion ($NI^{{\cdot}-}$) with a transient absorption band around 413 nm, via the intermolecular electron-transfer between NI moieties in the excited singlet state. In contrast, in a protic polar solvent mixture of $CH_3CN/H_2O$, a proton abstraction process occurred from $NI^{{\cdot}-}$ to generate the NI ketyl radical ($NIH^{\cdot}$), which showed a transient absorption band around 405 nm. The decay time constants of $NIH^{\cdot}$ were quite long compared to those of $NI^{{\cdot}-}$ in $CH_3CN$.

마이크로 에멀젼 계면을 통과하는 광유발전자의 양자수득률 (Quantum Yield of Photoinduced Electron Transfer Across Microemulsion Interfaces)

  • 박용태
    • 대한화학회지
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    • 제27권3호
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    • pp.213-217
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    • 1983
  • 태양에너지의 한 저장방법으로 녹색식물의 광합성을 모방한 계, 마이크로 에멀젼(microemulsion)을 고안하였으며, 이때 광에 의해서 유발된 전자가 계면을 통하는 능력을 측정하였다. 광증감제로 류테니늄비피리딘 착물$[Ru(bipy)_3]^{2+}$을 사용, 전자공여체 EDTA와 함께 물층에, 전자수용체 $HV^{2+}$(Hexadecyl violagan)이 계면에 각각 존재할 때 광에 의한 전자전이에 따르는 $HV^+$ 형성수득률은 0.12이였다. 또 계면에 $BNA^+$(Benzyl nicotinamide)를 넣고 유층에 아조(azo) 화합물을 넣었을 때는 azobenzene이 환원되었는데, 이때 양자수득률이 줄었다. (${\Phi}$ = 0.0016) 양이온 마이크로 에멀젼과 음이온 마이크로에멀젼의 광유발 전자전이 능력을 비교하였다. 광증감제로 유기염료인 로즈벤갈(Rose bengal)을 시험하였는데, 류테니늄착물보다 낮지 않았지만 광유발 전자가 계면에 전이되는 것을 알았다.

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