[1] Boutagy J, Thomas R. Olefin synthesis with organic phosphonate carbanions[J]. Chemical Society Reviews, 1974, 74(1): 87-99.
[2] Grochowski E, Hilton B D, Kupper R J, Michejda C J. Mechanism of the triphenylphosphine and diethyl azodicarboxylate induced dehydration reactions (Mitsunobu Reaction). The central role of pentavalent phosphorus intermediates[J]. Journal of the American Chemical Society, 1982, 104(24): 6874-6877.
[3] Mukaiyama V T. Die oxidations-reduktions-kondensation[J]. Angewandte Chemie-International Edition, 1976, 88(4): 111-120.
[4] Appel R. Tertiary phosphane/tetrachloromethane, a versatile reagent for chlorination, dehydration, and P-N linkage[J]. Angewandte Chemie-International Edition, 1975, 14(12): 801-811.
[5] Staudinger H, Meyer J. Uber neue organische phosphorverbindungen Ⅲ. phosphinmethylenderivate und phosphinimine[J]. Journal of Helvetica Chimica Acta, 1919, 2(1): 635-646.
[6] Suzuki A. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998[J]. Journal of Organometallic Chemistry, 1999, 576(1): 147-168.
[7] Boltzi D F, Mellon R G. Determination of phosphorus, germanium, silicon, and arsenic by the heteropoly blue method[J]. Analytical Chemistry, 1947, 19(11): 873-877.
[8] Haky J E, Baird D M, Falzone S. Revrsed phase high performance liquid chromatographic analysis of triphenylphosphine in a reaction mixture[J]. Analytical Letters, 1989, 22(11): 2637-2651.
[9] Szmant H H, Cox O. The acid-catalyzed reaction of triphenylphosphine with sulfoxides[J]. The Journal of Origanic Chemistry, 1966, 31(5): 1595-1598.
[10] Rao V R S, Aravamudan G. Oxidimetric determination of triphenylphosphine[J]. Talanta, 1969, 16(12): 1594-1596.
[11] Lin V S, Chen W, Xian M, Chang C J. Chemical probes for molecular imaging and detection of hydrogen sulfide and reactive sulfur species in biological systems[J]. Chemical Society Reviews, 2015, 44(14): 4596-4618.
[12] Vendrell M, Zhai D, Er J C, Chang Y T. Combinatorial strategies in fluorescent probe development[J]. Chemical Reviews, 2012, 112(8): 4391-4420.
[13] Paulsen C E, Carroll K S. Cysteine-mediated redox signaling: chemistry, biology, and tools for discovery[J]. Chemical Reviews, 2013, 113(7): 4633-4679.
[14] Bessette A, Hanan G S. Design, synthesis and photophysical studies of dipyrromethene-based materials: insights into their applications in organic photovoltaic devices[J]. Chemical Society Reviews, 2014, 43(10): 3342-3405.
[15] Kaur M, Choi D H. Diketopyrrolopyrrole: brilliant red pigment dye-based fluorescent probes and their applications[J]. Chemical Society Reviews, 2015, 44(1): 58-77.
[16] Lee M H, Yang Z, Lim C W, Lee Y H, Dongbang S, Kang C, Kim J S. Disulfide-cleavage-triggered chemosensors and their biological applications[J]. Chemical Reviews, 2013, 113(7): 5071-5109.
[17] Ni Y, Wu J S. Far-red and near infrared BODIPY dyes: synthesis and applications for fluorescent pH probes and bio-imaging[J]. Organic Biomolecular Chemistry, 2014, 12(23): 3774-3791.
[18] Chen X Q, Tian X Z, Shin I, Yoon J. Fluorescent and luminescent probes for detection of reactive oxygen and nitrogen species[J]. Chemical Society Reviews, 2011, 40(9): 4783-4804.
[19] Chen X, Pradhan T, Wang F, Kim J S, Yoon J. Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives[J]. Chemical Reviews, 2012, 112(3): 1910-1956.
[20] Yin J, Hu Y, Yoon J. Fluorescent probes and bioimaging: alkali metals, alkaline earth metals and pH[J]. Chemical Society Reviews, 2015, 44(14): 4619-4644.
[21] Yu F B, Han X Y, Chen L X. Fluorescent probes for hydrogen sulfide detection and bioimaging[J]. Chemical Communications, 2014, 50(82): 12234-12249.
[22] Carter K P, Young A M, Palmer A E. Fluorescent sensors for measuring metal Ions in living systems[J]. Chemical Reviews, 2014, 114(8): 4564-4601
[23] Zhu H, Fan J L, Wang B H, Peng X J. Fluorescent, MRI, and colorimetric chemical sensors for the first-row d-block metal ions[J]. Chemical Society Reviews, 2015, 44(13): 4337-4366.
[24] Sahoo S K, Sharma D, Bera R K, Crisponi G, Callan J F. Iron(Ⅲ) selective selective molecular and supramolecular fluorescent probes[J]. Chemical Society Reviews, 2012, 41(21): 7195-7227.
[25] Yang Y M, Zhao Q, Feng W, Li F Y. Luminescent chemodosimeters for bioimaging[J]. Chemical Reviews, 2013, 113(1): 192-270.
[26] Liu Z P, He W J, Guo Z J. Metal coordination in photoluminescent sensing[J]. Chemical Society Reviews, 2013, 42(4): 1568-1600.
[27] Jung H S, Chen X Q, Kim J S, Yoon J. Recent progress in luminescent and colorimetric chemosensors for detection of thiols[J]. Chemical Society Reviews, 2013, 42(14): 6019-6031.
[28] Wang F, Wang L, Chen X Q, Yoon J Y. Recent progress in the development of fluorometric and colorimetric chemosensors for detection of cyanide ions[J]. Chemical Society ReviewsL, 2014, 43(13): 4312-4324.
[29] Guo Z Q, Park S, Yoon J Y, Shin I. Recent progress in the development of near-infrared fluorescent probes for bioimaging applications[J]. Chemical Society Reviews, 2014, 43(1): 16-29.
[30] Yin C X, Huo F J, Zhang J J, Manez M R, Yang Y T, Lv H G, Li S D. Thiol-addition reactions and their applications in thiol recognition[J]. Chemical Society Reviews, 2013, 42(14): 6032-6059.
[31] Prier C K, Rankic D A, MacMillan D W C. Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis[J]. Chemical Reviews, 2013, 113(7): 5322-5363.
[32] Liu C Y, Wu H F, Wang Z K, Shao C X, Zhu B C, Zhang X L. A fast-response, highly sensitive and selective, fluorescent probe for the ratiometric imaging of nitroxyl in living cells[J]. Chemical Communications, 2014, 50(45): 6013-6016.
[33] Liu P, Jing X T, Yu F B, Lv C J, Chen L X. A near-infrared fluorescent probe for the selective detection of HNO in living cells and in vivo[J]. Analyst, 2015, 140(13): 4576-4583.
[34] Zhang D, Chen W, Miao Z R, Ye Y, Zhao Y F, King S B, Xian M. A reductive ligation based fluorescent probe for s-nitrosothiols[J]. Chemical Communications, 2014, 50(37): 4806-4809.
[35] Jing X T, Yu F B, Chen L X. Visualization of nitroxyl (HNO) in vivo via a lysosome-targetable near-infrared fluorescent probe[J]. Chemical Communications, 2014, 50(91): 14253-14256.
[36] Schilling C I, Jung N, Biskup M, Schepers U, Brase S. Bioconjugation via azide-staudinger ligation: an overview[J]. Chemical Society Reviews, 2011, 40(9): 4840-4871.
[37] Sletten E M, Bertozzi C R. Bioorthogonal chemistry: fishing for selectivity in a sea of functionality[J]. Angewandte Chemie-International Edition, 2009, 48(38): 6974-6998.
[38] Lemieux G A, Graffenried C L d, Bertozzi C R. A fluorogenic dye activated by the staudinger ligation[J]. Journal of the American Chemical Society, 2003, 125(16): 4708-4709.
[39] Lin F L, Hoyt H M, Halbeek H V, Bergman R G, Bertozzi C R. Mechanistic investigation of the staudinger ligation[J]. Journal of the American Chemical Society, 2005, 127(8): 2686-2695.
[40] Chang P V, Prescher J A, Hangauer M J, Bertozzi C R. Imaging cell surface glycans with bioorthogonal chemical reporters[J]. Journal of the American Chemical Society, 2007, 129(27): 8400-8401.
[41] Cohen A S, Dubikovskaya E A, Rush J S, Bertozzi C R. Real-time bioluminescence imaging of glycans on live cells[J]. Journal of the American Chemical Society, 2010, 132(25): 8563-8565.
[42] Brase S, Gil C, Knepper K, Zimmermann V. Organic azides: an exploding diversity of a unique class of compounds[J]. Angewandte Chemie-International Edition, 2005, 44(33): 5188-5240.
[43] Zhang Y L, Shao X M, Wang Y, Pan F C, Kang R X, Peng F F, Huang Z T, Zhang W J, Zhao W L. Dual emission channels for sensitive discrimination of Cys/Hcy and GSH in plasma and cells[J]. Chemical Communications, 2015, 51(20): 4245-4248.
[44] Shao X M, Kang R X, Zhang Y L, Huang Z T, Peng F F, Zhang J, Wang Y, Pan F C, Zhang W J, Zhao W L. Highly selective and sensitive 1 amino BODIPY-based red fluorescent probe for thiophenols with high off-to-on contrast ratio[J]. Analytical Chemistry, 2015, 87(1): 399-405.
[45] Kang R X, Shao X M, Peng F F, Zhang Y L, Sun G T, Zhao W L, Jiang X D. A highly selective turn-on fluorescent chemosensor for Al3+ imaging in living cells via through-bond energy transfer[J]. RSC Advances, 2013, 3(43): 21033-21038.
[46] Jiang X D, Zhang J, Shao X M, Zhao W L. A selective fluorescent turn-on NIR probe for cysteine[J]. Organic Biomolecular Chemistry, 2012, 10(10): 1966-1968.
[47] Zhang J, Jiang X D, Shao X M, Zhao J L, Su Y J, Xi D M, Yu H F, Yue S, Xiao L J, Zhao W L. A turn-on NIR fluorescent probe for the detection of homocysteine over cysteine[J]. RSC Advances, 2014, 4(96): 54080-54083.
[48] Liu B, Wang H, Wang T S, Bao Y Y, Du F F, Tian J, Li Q B, Bai R K. A new ratiometric ESIPT sensor for detection of palladium species in aqueous solution[J]. Chemical Communications, 2012, 48(23): 2867-2869.
[49] Liu Y, Yu D H, Ding S S, Xiao Q, Guo J, Feng G Q. Rapid and ratiometric fluorescent detection of cysteine with high selectivity and sensitivity by a simple and readily available probe[J]. ACS Applied Materials Interfaces, 2014, 6(20): 17543-17550.
[50] Chen S, Hou P, Zhou B J, Song X Z, Wu J S, Zhang H Y, Foley J W. A red fluorescent probe for thiols based on 3-hydroxyflavone and its application in living cell imaging[J]. RSC Advances, 2013, 3(29): 11543-11546.
[51] Liu Y, Feng G Q. A visible light excitable colorimetric and fluorescent ESIPT probe for rapid and selective detection of hydrogen sulfide[J]. Organic Biomolecular Chemistry, 2014, 12(3): 438-445.
[52] Nijveldt R J, Nood E V, Hoorn D E V, Boelens P G, Norren K V, Leeuwen P A V. Flavonoids: a review of probable mechanisms of action and potential applications[J]. The American Journal of Clinical Nutrition, 2001, 74(4): 418-425.
[53] Chevalier K, Grun A, Stamm A, Schmitt Y, Gerhards M, Diller R. ESIPT and photodissociation of 3-hydroxychromone in solution: photoinduced processes studied by static and time-resolved UV/Vis, fluorescence, and IR spectroscopy[J]. The Journal of Physical Chemistry A, 2013, 117(44): 11233-11245.
[54] Liu B, Wang J P, Zhang G, Bai R K, Pang Y. Flavone-based ESIPT ratiometric chemodosimeter for detection of cysteine in living cells[J]. ACS Applied Materials Interfaces, 2014, 6(6): 4402-4407.
[55] Lan M H, Wu J S, Liu W M, Zhang H Y, Zhang W J, Zhuang X Q, Wang P F. Highly sensitive fluorescent probe for thiols based on combination of PET and ESIPT mechanisms[J]. Sensors and Actuators B: Chemical, 2011, 156(1): 332-337.
[56] Shynkar V V, Klymchenko A S, Kunzelmann C, Duportail G, Muller C D, Demchenko A P, Freyssinet J M, Mely Y. Fluorescent biomembrane probe for ratiometric detection of apoptosis[J]. Journal of the American Chemical Society, 2007, 129(7): 2187-2193. |