+++амер. хим. общ 2-СПАСИБО ВСЕМ

[suprachemister]

Дорогие коллеги , прошу вас дать почитать еще парочку статей по обзору... Буду очень благодарен

1.A Ratiometric Fluorescence Probe for Selective Visual Sensing of Zn2+
Ayyappanpillai Ajayaghosh, Priya Carol, and Sivaramapanicker Sreejith
J. Am. Chem. Soc., 2005, 127 (43), pp 14962–14963

Код: Выделить всё

http://dx.doi.org/10.1021/ja054149s

2.Esterase-Activated Two-Fluorophore System for Ratiometric Sensing of Biological Zinc(II)
Carolyn C. Woodroofe, Annie C. Won, and Stephen J. Lippard
Inorg. Chem., 2005, 44 (9), pp 3112–3120

Код: Выделить всё

http://dx.doi.org/10.1021/ic048789s

3.Chemical Tools for Biomolecular Imaging
Nils Johnsson and Kai Johnsson
ACS Chem. Biol., 2007, 2 (1), pp 31–38

Код: Выделить всё

http://dx.doi.org/10.1021/cb6003977

4.Fluorescence-Based Zinc Ion Sensor for Zinc Ion Release from Pancreatic Cells
Georgeta Crivat, Kazuya Kikuchi, Tetsuo Nagano, Tsvia Priel, Michal Hershfinkel, Israel Sekler, Nitsa Rosenzweig, and Zeev Rosenzweig
Anal. Chem., 2006, 78 (16), pp 5799–5804

Код: Выделить всё

http://dx.doi.org/10.1021/ac060764i

5.Switching of Intramolecular Charge Transfer in Cruciforms: Metal Ion Sensing
James N. Wilson and Uwe H. F. Bunz
J. Am. Chem. Soc., 2005, 127 (12), pp 4124–4125

Код: Выделить всё

http://dx.doi.org/10.1021/ja050017n

6.Selective Zinc Sensor Molecules with Various Affinities for Zn2+, Revealing Dynamics and Regional Distribution of Synaptically Released Zn2+ in Hippocampal Slices
Kensuke Komatsu, Kazuya Kikuchi, Hirotatsu Kojima, Yasuteru Urano, and Tetsuo Nagano
J. Am. Chem. Soc., 2005, 127 (29), pp 10197–10204

Код: Выделить всё

http://dx.doi.org/10.1021/ja050301e

7.Methoxy-Substituted TQEN Family of Fluorescent Zinc Sensors
Yuji Mikata, Motoko Wakamatsu, Ayano Kawamura, Natsuko Yamanaka, Shigenobu Yano, Akira Odani, Kazuko Morihiro, and Satoshi Tamotsu
Inorg. Chem., 2006, 45 (23), pp 9262–9268

Код: Выделить всё

http://dx.doi.org/10.1021/ic060810x

8.Selective Fluorescence Zinc Ion Sensing and Binding Behavior of 4-Methyl-2,6-bis(((phenylmethyl)imino)methyl)phenol: Biological Application
Partha Roy, Koushik Dhara, Mario Manassero, Jagnyeswar Ratha, and Pradyot Banerjee
Inorg. Chem., 2007, 46 (16), pp 6405–6412

Код: Выделить всё

http://dx.doi.org/10.1021/ic700420w

9.Zinspy Sensors with Enhanced Dynamic Range for Imaging Neuronal Cell Zinc Uptake and Mobilization
Elizabeth M. Nolan, Jubin W. Ryu, Jacek Jaworski, Rodney P. Feazell, Morgan Sheng, and Stephen J. Lippard
J. Am. Chem. Soc., 2006, 128 (48), pp 15517–15528

Код: Выделить всё

http://dx.doi.org/10.1021/ja065759a

10.Bright Ideas for Chemical Biology
Luke D. Lavis and Ronald T. Raines
ACS Chem. Biol., 2008, 3 (3), pp 142–155

Код: Выделить всё

http://dx.doi.org/10.1021/cb700248m

11. 2-(2′-Hydroxyphenyl)benzoxazole-Containing Two-Photon-Absorbing Chromophores as Sensors for Zinc and Hydroxide Ions
Yanqing Tian, Ching-Yi Chen, Chang-Chung Yang, A. Cody Young, Sei-Hum Jang, Wen-Chang Chen and Alex K.-Y. Jen
Chem. Mater., 2008, 20 (5), pp 1977–1987

Код: Выделить всё

http://dx.doi.org/10.1021/cm702527m

12.Development of a Zinc Ion-Selective Luminescent Lanthanide Chemosensor for Biological Applications
Kenjiro Hanaoka, Kazuya Kikuchi, Hirotatsu Kojima, Yasuteru Urano, and Tetsuo Nagano
J. Am. Chem. Soc., 2004, 126 (39), pp 12470–12476

Код: Выделить всё

http://dx.doi.org/10.1021/ja0469333

13.Midrange Affinity Fluorescent Zn(II) Sensors of the Zinpyr Family: Syntheses, Characterization, and Biological Imaging Applications
Elizabeth M. Nolan, Jacek Jaworski, Maryann E. Racine, Morgan Sheng, and Stephen J. Lippard
Inorg. Chem., 2006, 45 (24), pp 9748–9757

Код: Выделить всё

http://dx.doi.org/10.1021/ic061137e

14.Two-Photon Probes for Intracellular Free Metal Ions, Acidic Vesicles, And Lipid Rafts in Live Tissues
Hwan Myung Kim and Bong Rae Cho
Acc. Chem. Res., 2009, 42 (7), pp 863–872

Код: Выделить всё

http://dx.doi.org/10.1021/ar800185u

15.In Situ Imaging of Metals in Cells and Tissues
Reagan McRae, Pritha Bagchi, S. Sumalekshmy and Christoph J. Fahrni
Chem. Rev., 2009, 109 (10), pp 4780–4827

Код: Выделить всё

http://dx.doi.org/10.1021/cr900223a

[ifh]

1-5

[nikolay_ap]

14,15

14.pdf

15.pdf

[Demcha]

10-15

[ifh]

6-10

[Demcha]

6-9