The Role of H-Bonds in the Excited-State Properties of Multichromophoric Systems: Static and Dynamic Aspects

被引:7
作者
Fresch, Elisa [1 ]
Collini, Elisabetta [1 ]
机构
[1] Univ Padua, Dept Chem Sci, Via Marzolo 1, I-35131 Padua, Italy
来源
MOLECULES | 2023年 / 28卷 / 08期
关键词
hydrogen bonds; ultrafast dynamics; 2D electronic spectroscopy; multichromophoric systems; excited-state dynamics; DOUBLE-PROTON-TRANSFER; PHOTOINDUCED ELECTRON-TRANSFER; ULTRAFAST RELAXATION DYNAMICS; PIGMENT-PROTEIN INTERACTIONS; LIGHT-HARVESTING PROTEIN; HYDROGEN-BOND; RADIATIONLESS DEACTIVATION; VIBRATIONAL DYNAMICS; 2D-IR SPECTROSCOPY; AB-INITIO;
D O I
10.3390/molecules28083553
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Given their importance, hydrogen bonds (H-bonds) have been the subject of intense investigation since their discovery. Indeed, H-bonds play a fundamental role in determining the structure, the electronic properties, and the dynamics of complex systems, including biologically relevant materials such as DNA and proteins. While H-bonds have been largely investigated for systems in their electronic ground state, fewer studies have focused on how the presence of H-bonds could affect the static and dynamic properties of electronic excited states. This review presents an overview of the more relevant progress in studying the role of H-bond interactions in modulating excited-state features in multichromophoric biomimetic complex systems. The most promising spectroscopic techniques that can be used for investigating the H-bond effects in excited states and for characterizing the ultrafast processes associated with their dynamics are briefly summarized. Then, experimental insights into the modulation of the electronic properties resulting from the presence of H-bond interactions are provided, and the role of the H-bond in tuning the excited-state dynamics and the related photophysical processes is discussed.
引用
收藏
页数:20
相关论文
共 128 条
[1]   How water-mediated hydrogen bonds affect chlorophyll a/b selectivity in Water-Soluble Chlorophyll Protein [J].
Agostini, Alessandro ;
Meneghin, Elena ;
Gewehr, Lucas ;
Pedron, Danilo ;
Palm, Daniel M. ;
Carbonera, Donatella ;
Paulsen, Harald ;
Jaenicke, Elmar ;
Collini, Elisabetta .
SCIENTIFIC REPORTS, 2019, 9 (1)
[2]   Time-resolved terahertz-Raman spectroscopy reveals that cations and anions distinctly modify intermolecular interactions of water [J].
Balos, Vasileios ;
Kaliannan, Naveen Kumar ;
Elgabarty, Hossam ;
Wolf, Martin ;
Kuehne, Thomas D. ;
Sajadi, Mohsen .
NATURE CHEMISTRY, 2022, 14 (09) :1031-+
[3]   Vibrational Dynamics of Hydrogen-Bonded Complexes in Solutions Studied with Ultrafast Infrared Pump-Probe Spectroscopy [J].
Banno, Motohiro ;
Ohta, Kaoru ;
Yamaguchi, Sayuri ;
Hirai, Satori ;
Tominaga, Keisuke .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (09) :1259-1269
[4]   Fluorescence Quenching of Hydrogen-Bonded Coumarin 102-Phenol Complex: Effect of Excited-State Hydrogen Bonding Strength [J].
Barman, Nabajeet ;
Singha, Debabrata ;
Sahu, Kalyanasis .
JOURNAL OF PHYSICAL CHEMISTRY A, 2013, 117 (19) :3945-3953
[5]   Time-resolved resonance Raman spectroscopy [J].
Bell, SEJ .
ANALYST, 1996, 121 (11) :R107-R120
[6]   Ultrafast transient absorption spectroscopy: principles and application to photosynthetic systems [J].
Berera, Rudi ;
van Grondelle, Rienk ;
Kennis, John T. M. .
PHOTOSYNTHESIS RESEARCH, 2009, 101 (2-3) :105-118
[7]   Quenching processes in hydrogen-bonded pairs: Interactions of excited fluorenone with alcohols and phenols [J].
Biczok, L ;
Berces, T ;
Linschitz, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (45) :11071-11077
[8]   Effects of molecular structure and hydrogen bonding on the radiationless deactivation of singlet excited fluorenone derivatives [J].
Biczók, L ;
Bérces, T ;
Inoue, H .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (20) :3837-3842
[9]   Coherent Two-Dimensional and Broadband Electronic Spectroscopies [J].
Biswas, Somnath ;
Kim, JunWoo ;
Zhang, Xinzi ;
Scholes, Gregory D. .
CHEMICAL REVIEWS, 2022, 122 (03) :4257-4321
[10]  
Branczyk A.M., 2013, ARXIV