BODIPY (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "BODIPY" in Czech language version.

Last modified: 18:37:34, 9 May 2025 (UTC)

Ref.Un. Ref.Website

Global rank Czech rank

3416doi.org

2^nd place

4^th place

2014nih.gov

5^th place

8^th place

33worldcat.org

4^th place

2^nd place

11adsabs.harvard.edu

14^th place

63^rd place

adsabs.harvard.edu (Global: 14^th place; Czech: 63^rd place)

Patrycja Stachelek; Abdulrahman A. Alsimaree; Rua B. Alnoman; Anthony Harriman; Julian G. Knight. Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A. 2017-03-16, s. 2096–2107. ISSN 1089-5639. doi:10.1021/acs.jpca.6b11131. PMID 28245114. Bibcode 2017JPCA..121.2096S.

doi.org (Global: 2^nd place; Czech: 4^th place)

K. Tram; H. Yan; H. A. Jenkins; S. Vassiliev; D. Bruce. The synthesis and crystal structure of unsubstituted 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY). Dyes and Pigments. 2009, s. 392–395. doi:10.1016/j.dyepig.2009.03.001.
A. Schmitt; B. Hinkeldey; M. Wild; G. Jung. Synthesis of the Core Compound of the BODIPY Dye Class: 4,4′-Difluoro-4-bora-(3a,4a)-diaza-s-indacene. Journal of Fluorescence. 2009. doi:10.1007/s10895-008-0446-7. PMID 19067126.
I. J. Arroyo; R. Hu; G. Merino; B. Z. Tang; E. Peña-Cabrera. The Smallest and One of the Brightest. Efficient Preparation and Optical Description of the Parent Borondipyrromethene System. The Journal of Organic Chemistry. 2009, s. 5719–5722. doi:10.1021/jo901014w. PMID 19572588.
Kevin Burgess. BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties. Chemical Reviews. 2007, s. 4891–4932. doi:10.1021/cr078381n. PMID 17924696.
Brandon R. Groves; Sarah M. Crawford; Travis Lundrigan; Chérif F. Matta; Shahin Sowlati-Hashjin; Alison Thompson. Synthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: Improved synthesis and functionalisation of the simplest BODIPY framework. Chemical Communications. 2013, s. 816–818. doi:10.1039/c2cc37480c. PMID 23235887.
Aurore Loudet and Kevin Burgess (2007): "BODIPY dyes and their derivatives: Syntheses and spectroscopic properties". Chemical Reviews, volume 107, issue 11, pages 4891–4932 doi:10.1021/cr078381n
Zhong-Hua Pan; Geng-Geng Luo; Jing-Wei Zhou; Jiu-Xu Xia; Kai Fang; Rui-Bo Wu. A simple BODIPY-aniline-based fluorescent chemosensor as multiple logic operations for the detection of pH and CO2 gas. Dalton Transactions. 2014, s. 8499–8507. doi:10.1039/C4DT00395K. PMID 24756338.
Patrycja Stachelek; Abdulrahman A. Alsimaree; Rua B. Alnoman; Anthony Harriman; Julian G. Knight. Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A. 2017-03-16, s. 2096–2107. ISSN 1089-5639. doi:10.1021/acs.jpca.6b11131. PMID 28245114. Bibcode 2017JPCA..121.2096S.
Dumitru Sirbu; Andrew C. Benniston; Anthony Harriman. One-Pot Synthesis of a Mono-O,B,N-strapped BODIPY Derivative Displaying Bright Fluorescence in the Solid State. Organic Letters. 2017-04-07, s. 1626–1629. ISSN 1523-7060. doi:10.1021/acs.orglett.7b00435. PMID 28319396.
Dumitru Sirbu; Saimir Luli; Jack Leslie; Fiona Oakley; Andrew C. Benniston. Enhanced in vivo Optical Imaging of the Inflammatory Response to Acute Liver Injury in C57BL/6 Mice Using a Highly Bright Near-Infrared BODIPY Dye. ChemMedChem. 2019-05-17, s. 995–999. ISSN 1860-7179. doi:10.1002/cmdc.201900181. PMID 30920173.
Toshiyuki Kowada; Hiroki Maeda; Kazuya Kikuchi. BODIPY-based probes for the fluorescence imaging of biomolecules in living cells. Chemical Society Reviews. 2015, s. 4953–4972. doi:10.1039/C5CS00030K. PMID 25801415.
Yong Ni; Jishan Wu. Far-red and near infrared BODIPY dyes: Synthesis and applications for fluorescent pH probes and bio-imaging. Organic & Biomolecular Chemistry. 2014, s. 3774–3791. doi:10.1039/c3ob42554a. PMID 24781214.
Heidi Abrahamse; Michael R. Hamblin. New photosensitizers for photodynamic therapy. Biochemical Journal. 2016, s. 347–364. doi:10.1042/BJ20150942. PMID 26862179.
Hua Lu; John Mack; Yongchao Yang; Zhen Shen. Structural modification strategies for the rational design of red/NIR region BODIPYs. Chemical Society Reviews. 2014, s. 4778–4823. doi:10.1039/C4CS00030G. PMID 24733589.
Jean Roncali. Molecular Bulk Heterojunctions: An Emerging Approach to Organic Solar Cells. Accounts of Chemical Research. 2009, s. 1719–1730. doi:10.1021/ar900041b. PMID 19580313.
Ha Na Kim; Wen Xiu Ren; Jong Seung Kim; Juyoung Yoon. Fluorescent and colorimetric sensors for detection of lead, cadmium, and mercury ions. Chemical Society Reviews. 2012, s. 3210–3244. doi:10.1039/C1CS15245A. PMID 22184584.

nih.gov (Global: 5^th place; Czech: 8^th place)

ncbi.nlm.nih.gov

A. Schmitt; B. Hinkeldey; M. Wild; G. Jung. Synthesis of the Core Compound of the BODIPY Dye Class: 4,4′-Difluoro-4-bora-(3a,4a)-diaza-s-indacene. Journal of Fluorescence. 2009. doi:10.1007/s10895-008-0446-7. PMID 19067126.
I. J. Arroyo; R. Hu; G. Merino; B. Z. Tang; E. Peña-Cabrera. The Smallest and One of the Brightest. Efficient Preparation and Optical Description of the Parent Borondipyrromethene System. The Journal of Organic Chemistry. 2009, s. 5719–5722. doi:10.1021/jo901014w. PMID 19572588.
Kevin Burgess. BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties. Chemical Reviews. 2007, s. 4891–4932. doi:10.1021/cr078381n. PMID 17924696.
Brandon R. Groves; Sarah M. Crawford; Travis Lundrigan; Chérif F. Matta; Shahin Sowlati-Hashjin; Alison Thompson. Synthesis and characterisation of the unsubstituted dipyrrin and 4,4-dichloro-4-bora-3a,4a-diaza-s-indacene: Improved synthesis and functionalisation of the simplest BODIPY framework. Chemical Communications. 2013, s. 816–818. doi:10.1039/c2cc37480c. PMID 23235887.
Zhong-Hua Pan; Geng-Geng Luo; Jing-Wei Zhou; Jiu-Xu Xia; Kai Fang; Rui-Bo Wu. A simple BODIPY-aniline-based fluorescent chemosensor as multiple logic operations for the detection of pH and CO2 gas. Dalton Transactions. 2014, s. 8499–8507. doi:10.1039/C4DT00395K. PMID 24756338.
Patrycja Stachelek; Abdulrahman A. Alsimaree; Rua B. Alnoman; Anthony Harriman; Julian G. Knight. Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A. 2017-03-16, s. 2096–2107. ISSN 1089-5639. doi:10.1021/acs.jpca.6b11131. PMID 28245114. Bibcode 2017JPCA..121.2096S.
Dumitru Sirbu; Andrew C. Benniston; Anthony Harriman. One-Pot Synthesis of a Mono-O,B,N-strapped BODIPY Derivative Displaying Bright Fluorescence in the Solid State. Organic Letters. 2017-04-07, s. 1626–1629. ISSN 1523-7060. doi:10.1021/acs.orglett.7b00435. PMID 28319396.
Dumitru Sirbu; Saimir Luli; Jack Leslie; Fiona Oakley; Andrew C. Benniston. Enhanced in vivo Optical Imaging of the Inflammatory Response to Acute Liver Injury in C57BL/6 Mice Using a Highly Bright Near-Infrared BODIPY Dye. ChemMedChem. 2019-05-17, s. 995–999. ISSN 1860-7179. doi:10.1002/cmdc.201900181. PMID 30920173.
Toshiyuki Kowada; Hiroki Maeda; Kazuya Kikuchi. BODIPY-based probes for the fluorescence imaging of biomolecules in living cells. Chemical Society Reviews. 2015, s. 4953–4972. doi:10.1039/C5CS00030K. PMID 25801415.
Yong Ni; Jishan Wu. Far-red and near infrared BODIPY dyes: Synthesis and applications for fluorescent pH probes and bio-imaging. Organic & Biomolecular Chemistry. 2014, s. 3774–3791. doi:10.1039/c3ob42554a. PMID 24781214.
Heidi Abrahamse; Michael R. Hamblin. New photosensitizers for photodynamic therapy. Biochemical Journal. 2016, s. 347–364. doi:10.1042/BJ20150942. PMID 26862179.
Hua Lu; John Mack; Yongchao Yang; Zhen Shen. Structural modification strategies for the rational design of red/NIR region BODIPYs. Chemical Society Reviews. 2014, s. 4778–4823. doi:10.1039/C4CS00030G. PMID 24733589.
Jean Roncali. Molecular Bulk Heterojunctions: An Emerging Approach to Organic Solar Cells. Accounts of Chemical Research. 2009, s. 1719–1730. doi:10.1021/ar900041b. PMID 19580313.
Ha Na Kim; Wen Xiu Ren; Jong Seung Kim; Juyoung Yoon. Fluorescent and colorimetric sensors for detection of lead, cadmium, and mercury ions. Chemical Society Reviews. 2012, s. 3210–3244. doi:10.1039/C1CS15245A. PMID 22184584.

worldcat.org (Global: 4^th place; Czech: 2^nd place)

Patrycja Stachelek; Abdulrahman A. Alsimaree; Rua B. Alnoman; Anthony Harriman; Julian G. Knight. Thermally-Activated, Delayed Fluorescence in O,B,O- and N,B,O-Strapped Boron Dipyrromethene Derivatives. The Journal of Physical Chemistry A. 2017-03-16, s. 2096–2107. ISSN 1089-5639. doi:10.1021/acs.jpca.6b11131. PMID 28245114. Bibcode 2017JPCA..121.2096S.
Dumitru Sirbu; Andrew C. Benniston; Anthony Harriman. One-Pot Synthesis of a Mono-O,B,N-strapped BODIPY Derivative Displaying Bright Fluorescence in the Solid State. Organic Letters. 2017-04-07, s. 1626–1629. ISSN 1523-7060. doi:10.1021/acs.orglett.7b00435. PMID 28319396.
Dumitru Sirbu; Saimir Luli; Jack Leslie; Fiona Oakley; Andrew C. Benniston. Enhanced in vivo Optical Imaging of the Inflammatory Response to Acute Liver Injury in C57BL/6 Mice Using a Highly Bright Near-Infrared BODIPY Dye. ChemMedChem. 2019-05-17, s. 995–999. ISSN 1860-7179. doi:10.1002/cmdc.201900181. PMID 30920173.

BODIPY (Czech Wikipedia)

adsabs.harvard.edu (Global: 14th place; Czech: 63rd place)

doi.org (Global: 2nd place; Czech: 4th place)

nih.gov (Global: 5th place; Czech: 8th place)

ncbi.nlm.nih.gov

worldcat.org (Global: 4th place; Czech: 2nd place)

adsabs.harvard.edu (Global: 14^th place; Czech: 63^rd place)

doi.org (Global: 2^nd place; Czech: 4^th place)

nih.gov (Global: 5^th place; Czech: 8^th place)

worldcat.org (Global: 4^th place; Czech: 2^nd place)