Time-Resolved Spectroscopy of Indigo and of a Maya Blue Simulant

被引:25
作者
Bernardino, N. D. [1 ,2 ]
Brown-Xu, S. [2 ]
Gustafson, T. L. [2 ]
de Faria, D. L. A. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim, Lab Espectroscopia Mol, CP 26077, BR-05513970 Sao Paulo, SP, Brazil
[2] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
基金
美国国家科学基金会; 巴西圣保罗研究基金会;
关键词
EXCITED-STATE CHARACTERIZATION; RAMAN-SPECTROSCOPY; ABSORPTION-SPECTROSCOPY; PICOSECOND SPECTROSCOPY; TRANS-THIOINDIGO; PROTON-TRANSFER; TRIPLET-STATE; DYNAMICS; SOLVENT; PHOTOCHEMISTRY;
D O I
10.1021/acs.jpcc.6b04681
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Maya Blue is a puzzling pigment found in objects produced by the ancient Maya civilization. It is a combination of indigo and palygorskite, and it is well-known for the high chemical and Photochemical stability of the dye promoted by the clay confined environment. This pigment has survived over 1500 years, and it was first thought to be purely inorganic. The reasons for such stability have been investigated over the past years, and it may involve hydrogen bonds, complexation, and oxidation to dehydroindigo. However, these theories are not completely understood, and more evidence about indigo/palygorskite interactions must be obtained: in this, study indigo and a Maya Blue simulant pigment were, for the first time, studied by transient absorption (TA) and time-resolved infrared (TRIR) spectroscopy. From such analysis it was possible to investigate the electronic-excited states of indigo and the photochemistry behavior of the dye when interacting with the palygorskite. Concerning the TRIR measurements, the shifts of the C=O and N-H vibrations indicate that hydrogen bonds are formed involving the dye and the coordinated water molecules present in the clay. Furthermore, aired shift is observed in the absorption of electronic ground state (50 nm) and also in the electronic excited-state (27 nm) of Maya Bite simulant, :suggesting that the excited states are stabilized by the clay. Indigo in DMSO solution presents a lifetime of ca. 120 ps while in the day it becomes much shorter, ca. 3 ps. The shorter lifetime and also the red shift, observed in the TA results suggest a stabilization of the first electronic excited state, which promotes a more efficient energy relation through conical intersection and, as a consequence, a fastet excited state decay. Such factors can be important for the Maya. Blue photostability, as they are also believed to be responsible for the high photostability of DNA and melanin.
引用
收藏
页码:21905 / 21914
页数:10
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