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首页> 外文期刊>The Journal of Chemical Physics >Planarizing cytosine: The S-1 state structure, vibrations, and nonradiative dynamics of jet-cooled 5,6-trimethylenecytosine
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Planarizing cytosine: The S-1 state structure, vibrations, and nonradiative dynamics of jet-cooled 5,6-trimethylenecytosine

机译:平面化胞嘧啶:喷射5,6-三甲基二核的S-1状态结构,振动和非接壤动态

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We measure the S-0 -> S-1 spectrum and time-resolved S1 state nonradiative dynamics of the "clamped" cytosine derivative 5,6-trimethylenecytosine (TMCyt) in a supersonic jet, using two-color resonant two-photon ionization (R2PI), UV/UV holeburning, and ns time-resolved pump/delayed ionization. The experiments are complemented with spin-component scaled second-order approximate coupled cluster (SCS-CC2), time-dependent density functional theory, and multi-state second-order perturbation-theory (MS-CASPT2) ab initio calculations. While the R2PI spectrum of cytosine breaks off similar to 500 cm(-1) above its 0(0)(0) band, that of TMCyt extends up to + 4400 cm(-1) higher, with over a hundred resolved vibronic bands. Thus, clamping the cytosine C-5-C-6 bond allows us to explore the S-1 state vibrations and S-0 -> S-1 geometry changes in detail. The TMCyt S-1 state out-of-plane vibrations nu(1)', nu(3)', and nu(5)' lie below 420 cm(-1), and the in-plane nu(11)', nu(12)', and nu(23)' vibrational fundamentals appear at 450, 470, and 944 cm(-1). S-0 -> S-1 vibronic simulations based on SCS-CC2 calculations agree well with experiment if the calculated nu(1)', nu(3)', and nu(5)' frequencies are reduced by a factor of 2-3. MS-CASPT2 calculations predict that the ethylene-type S-1 (sic) S-0 conical intersection (CI) increases from + 366 cm(-1) in cytosine to > 6000 cm(-1) in TMCyt, explaining the long lifetime and extended S-0 -> S-1 spectrum. The lowest-energy S-1 (sic) S-0 CI of TMCyt is the "amino out-of-plane" (OPX) intersection, calculated at + 4190 cm(-1). The experimental S-1 (sic) S-0 internal conversion rate constant at the S-1(v' = 0) level is k(IC) = 0.98-2.2.10(8) s(-1), which is similar to 10 times smaller than in 1-methylcytosine and cytosine. The S-1(v' = 0) level relaxes into the T-1((3)pi pi*) state by intersystem crossing with k(ISC) = 0.41-1.6.10(8) s(-1). The T-1 state energy is measured to lie 24 580 +/- 560 cm(-1) above the S0 state. The S-1(v' = 0) lifetim
机译:我们测量S-0 - > S-1频谱和时间分辨的S1状态非分辨的S1状态非旋转动力学在超音射流中的“夹紧”胞嘧啶衍生物5,6-三甲基二核(TMCYT),使用双色共振双光子电离( R2PI),UV / UV Holburning和NS时间分辨泵/延迟电离。实验互补地,旋转组分缩放的二阶近似耦合集群(SCS-CC2),时间依赖性密度函数理论和多状态二阶扰动理论(MS-CASPT2)AB Initio计算。虽然胞嘧啶的R2PI光谱在其0(0)频带上方类似于500cm(-1),但TMCYT的速度高达+ 4400cm(-1)升高,具有超过一百个分辨的振动带。因此,夹紧胞嘧啶C-5-C-6键使我们能够详细探讨S-1状态振动和S-0 - > S-1几何形状。 TMCYT S-1状态外平面振动NU(1)',NU(3)'和NU(5)'位于420厘米(-1)以下,以及面内NU(11)', Nu(12)'和Nu(23)'振动基本面出现在450,470和944厘米(-1)。基于SCS-CC2计算的S-0 - > S-1振动模拟对实验很好,如果计算出的NU(1)',NU(3)'和NU(5)'频率减少了2- 3. MS-CASPT2计算预测乙烯-S-1(SiC)S-0锥形交叉点(CI)在TMCYT中从胞嘧啶中的+ 366厘米(-1)增加到> 6000cm(-1),解释了长寿并扩展S-0 - > S-1光谱。 TMCYT的最低能量S-1(SiC)S-0 CI是“氨基外平面”(OPX)交叉点,计算为+ 4190cm(-1)。在S-1(V'= 0)水平下的实验S-1(SiC)S-0内部转化率常数是K(IC)= 0.98-2.2.10(8)S(-1),其相似比1-甲基胞嘧啶和胞嘧啶小的10倍。 S-1(V'= 0)水平通过与K(ISC)= 0.41-1.6.10(8)S(-1)的k(ISC)交叉来放松进入T-1((3)PI PI *)状态。测量T-1状态能量以在S0状态上方的24 580 +/- 560cm(-1)。 S-1(V'= 0)Lifetim

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