Photochemistry of Tetrasulfur Tetranitride: Laser Flash Photolysis and Quantum Chemical Study

被引:5
作者
Pritchina, Elena A. [1 ,3 ]
Terpilovskaya, Dania S. [1 ,3 ]
Tsentalovich, Yuri P. [2 ,3 ]
Platz, Matthew S. [4 ]
Gritsan, Nina P. [1 ,3 ]
机构
[1] Russian Acad Sci, Inst Chem Kinet & Combust, Novosibirsk 630090, Russia
[2] Russian Acad Sci, Siberian Branch, Int Tomog Ctr, Novosibirsk 630090, Russia
[3] Novosibirsk State Univ, Natl Res Univ, Novosibirsk 630090, Russia
[4] Ohio State Univ, Dept Chem, Columbus, OH 43210 USA
基金
俄罗斯基础研究基金会; 美国国家科学基金会;
关键词
AB-INITIO; THIAZYL RADICALS; CRYSTAL-STRUCTURE; BOTTOM-UP; NITROGEN; THIONITROSO; CHEMISTRY; SPIN; 1,3,2,4-BENZODITHIADIAZINES; VAPORIZATION;
D O I
10.1021/ic3000153
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The photochemistry of tetrasulfur tetranitride (1) was studied in hexane solution by the laser flash photolysis technique (LFP). The experimental findings were interpreted E.A.; Gritsan, NP.; Bally, T.; Zibarev, A.V. Inorg. Chem. 2009, using the results of previous matrix isolation studies (Pritchina, 48, 4075) and high-level quantum chemical calculations. LFP produces two primary intermediates, one of which is the boatshaped 8-membered cyclic compound (2) and the other is the 6-membered S3N3 cyclic compound carrying an exocyclic (S)-N=S group (3). The primary products 2 and 3 absorb a second photon and undergo transformation to the 6-membered S3N3 cycle carrying an exocyclic (N)-S N group (4), which is very unstable and converts back to intermediate 3. The quantum yield of the primary product formation is close to unity even though the quantum yield of photodegradation of 1 is low (similar to 0.01). Thus, 1 is a photochromic compound undergoing in solution the thermally reversible photochemical isomerization. The mechanism of the photochromic process was established, and the rate constants of the elementary reactions were measured.
引用
收藏
页码:4747 / 4755
页数:9
相关论文
共 85 条
[71]   CRYSTAL AND MOLECULAR STRUCTURE OF SULFUR NITRIDE, S4N4 [J].
SHARMA, BD ;
DONOHUE, J .
ACTA CRYSTALLOGRAPHICA, 1963, 16 (09) :891-&
[72]   New polysulfur-nitrogen heterocycles as precursors of thiazyl radicals [J].
Shuvaev, KV ;
Bagryansky, VA ;
Gritsan, NP ;
Makarov, AY ;
Molin, YN ;
Zibarev, AV .
MENDELEEV COMMUNICATIONS, 2003, (04) :178-179
[73]  
Sperling D, 1996, LIEBIGS ANN-RECL, P1615
[74]   SPECTROSCOPIC DETECTION AND REACTIONS OF A THIONITROSO COMPOUND [J].
TAKAHASHI, M ;
OKAZAKI, R ;
INAMOTO, N ;
SUGAWARA, T ;
IWAMURA, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (05) :1830-1837
[75]   NEW REACTIONS OF A THIONITROSOARENE [J].
TAKAHASHI, M ;
OKAZAKI, R ;
INAMOTO, N .
CHEMISTRY LETTERS, 1989, (12) :2087-2090
[76]   Quantum mechanical continuum solvation models [J].
Tomasi, J ;
Mennucci, B ;
Cammi, R .
CHEMICAL REVIEWS, 2005, 105 (08) :2999-3093
[77]  
Torroba T, 1999, J PRAK CHEM-CHEM ZTG, V341, P99, DOI 10.1002/(SICI)1521-3897(199902)341:2<99::AID-PRAC99>3.0.CO
[78]  
2-Z
[79]   Study of the chemistry of ortho- and para-biphenylnitrenes by laser flash photolysis and time-resolved IR experiments and by B3LYP and CASPT2 calculations [J].
Tsao, ML ;
Gritsan, N ;
James, TR ;
Platz, MS ;
Hrovat, DA ;
Borden, WT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (31) :9343-9358
[80]   Metallization of a Hypervalent Radical Dimer: Molecular and Band Perspectives [J].
Tse, John S. ;
Leitch, Alicea A. ;
Yu, Xueyang ;
Bao, Xuezhao ;
Zhang, Sijia ;
Liu, Qingqing ;
Jin, Changqing ;
Secco, Richard A. ;
Desgreniers, Serge ;
Ohishi, Yasuo ;
Oakley, Richard T. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (13) :4876-4886