Abstract
Rhodamine-based chemosensors have sparked considerable interest in recent years due to their remarkable photophysical properties, which include high absorption coefficients, exceptional quantum yields, improved photostability, and significant red shifts. This article presents an overview of the diverse fluorometric, and colorimetric sensors produced from rhodamine, as well as their applications in a wide range of fields. The ability of rhodamine-based chemosensors to detect a wide range of metal ions, including Hg+2, Al3+, Cr3+, Cu2+, Fe3+, Fe2+, Cd2+, Sn4+, Zn2+, and Pb2+, is one of their major advantages. Other applications of these sensors include dual analytes, multianalytes, and relay recognition of dual analytes. Rhodamine-based probes can also detect noble metal ions such as Au3+, Ag+, and Pt2+. They have been used to detect pH, biological species, reactive oxygen and nitrogen species, anions, and nerve agents in addition to metal ions. The probes have been engineered to undergo colorimetric or fluorometric changes upon binding to specific analytes, rendering them highly selective and sensitive by ring-opening via different mechanisms such as Photoinduced Electron Transfer (PET), Chelation Enhanced Fluorescence (CHEF), Intramolecular Charge Transfer (ICT), and Fluorescence Resonance Energy Transfer (FRET). For improved sensing performance, light-harvesting dendritic systems based on rhodamine conjugates has also been explored for enhanced sensing performance. These dendritic arrangements permit the incorporation of numerous rhodamine units, resulting in an improvement in signal amplification and sensitivity. The probes have been utilised extensively for imaging biological samples, including imaging of living cells, and for environmental research. Moreover, they have been combined into logic gates for the construction of molecular computing systems. The usage of rhodamine-based chemosensors has created significant potential in a range of disciplines, including biological and environmental sensing as well as logic gate applications. This study focuses on the work published between 2012 and 2021 and emphasises the enormous research and development potential of these probes.
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Abbreviations
- AAS:
-
Atomic Absorption Spectroscopy
- ADP:
-
Adenosine Diphosphate
- AFM:
-
Atomic Force Microscopy
- AMP:
-
Adenosine Monophosphate
- BR:
-
Britton-Robinson
- CHEF:
-
Chelation Induced Enhanced Fluorescence
- Cys:
-
Cysteine
- DCP:
-
Diethyl chlorophosphate
- EDTA:
-
Ethylenediamine tetraacetic acid
- ESI-MS:
-
Electron spray ionisation Mass Spectrometry
- FRET:
-
Forster Resonance Energy Transfer
- GSH:
-
Glutathione
- Hcy:
-
Homocysteine
- HEPES:
-
(4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acid)
- ICP-AES:
-
Inductively Coupled Plasma Atomic Emission Spectrometry
- ICP-MS:
-
Inductively Coupled Plasma Mass Spectrometry
- ICT:
-
Intramolecular Charge Transfer
- IR:
-
Infra-red
- KCN:
-
Potassium cyanide
- LOD:
-
Limit of Detection
- NMR:
-
Nuclear Magnetic Resonance
- NIR:
-
Near Infra-red
- PET:
-
Photoinduced Electron Transfer
- TD-DFT:
-
Time-dependent Density Functional Theory
- TBACN:
-
Tetrabutyl ammonium cyanide
- TBAI:
-
Tetrabutyl ammonium iodide
- TFA:
-
Trifluoroacetic acid
- UV/Vis:
-
Ultraviolet- Visible
- PTA:
-
Phosphotungstic acid
- PAMAM:
-
-Polyamidoamines
References
Chen X, Pradhan T, Wang F et al (2012) Fluorescent chemosensors based on spiroring-opening of xanthenes and related derivatives. Chem Rev 112:1910–1956. https://doi.org/10.1021/cr200201z
Dujols V, Ford F, Czarnik AW (1997) A long-wavelength fluorescent chemodosimeter selective for Cu(II) ion in water. J Am Chem Soc 119:7386–7387. https://doi.org/10.1021/ja971221g
Kim HN, Lee MH, Kim HJ et al (2008) A new trend in rhodamine-based chemosensors: Application of spirolactam ring-opening to sensing ions. Chem Soc Rev 37:1465–1472. https://doi.org/10.1039/b802497a
Moon H, Park J, Tae J (2016) Fluorescent probes based on rhodamine hydrazides and hydroxamates. Chem Rec 16:124–140. https://doi.org/10.1002/tcr.201500226
Carta CL (2014) The effects of medium on the UV-induced photodegradation of the effects of medium on the UV-induced photodegradation of rhodamine B Dye Rhodamine B Dye. https://doi.org/10.21220/s2-pvy5-9w91
Wang L, Du W, Hu Z et al (2019) Hybrid rhodamine fluorophores in the Visible/NIR region for biological imaging. Angew Chemie - Int Ed 58:14026–14043. https://doi.org/10.1002/anie.201901061
Chi W, Qi Q, Lee R et al (2020) A unified push–pull model for understanding the ring-opening mechanism of rhodamine dyes. J Phys Chem C 124:3793–3801
Beija M, Afonso CAM, Martinho JMG (2009) Synthesis and applications of rhodamine derivatives as fluorescent probes. Chem Soc Rev 38:2410–2433. https://doi.org/10.1039/b901612k
Li N, Liu M, Yin W et al (2011) Recent progress in rhodamine-based “OFF-ON” fluorescent probes. Chinese J Org Chem 31:39–53
Choudhury N, De P (2021) Recent progress in pendant rhodamine-based polymeric sensors for the detection of copper, mercury and iron ions. J Macromol Sci Part A Pure Appl Chem 58:835–848. https://doi.org/10.1080/10601325.2021.1960172
Bai CB, Wang WG, Zhang J et al (2020) A fluorescent and colorimetric chemosensor for Hg2+ based on rhodamine 6G with a two-step reaction mechanism. Front Chem 8:1–7. https://doi.org/10.3389/fchem.2020.00014
Formica M, Fusi V, Giorgi L, Micheloni M (2012) New fluorescent chemosensors for metal ions in solution. Coord Chem Rev 256:170–192. https://doi.org/10.1016/j.ccr.2011.09.010
Dongare PR, Gore AH (2021) Recent advances in colorimetric and fluorescent chemosensors for ionic species: design, principle and optical signalling mechanism. ChemistrySelect 6:5657–5669. https://doi.org/10.1002/slct.202101090
Sharma S, Ghosh KS (2021) Recent advances (2017–20) in the detection of copper ion by using fluorescence sensors working through transfer of photo-induced electron (PET), excited-state intramolecular proton (ESIPT) and Förster resonance energy (FRET). Spectrochim Acta - Part A Mol Biomol Spectrosc 254:119610. https://doi.org/10.1016/j.saa.2021.119610
Suganya S, Naha S, Velmathi S (2018) A critical review on colorimetric and fluorescent probes for the sensing of analytes via relay recognition from the year 2012–17. ChemistrySelect 3:7231–7268. https://doi.org/10.1002/slct.201801222
Hazra S, Balaji S, Banerjee M et al (2014) A PEGylated-rhodamine based sensor for “turn-on” fluorimetric and colorimetric detection of Hg2+ ions in aqueous media. Anal Methods 6:3784–3790. https://doi.org/10.1039/c4ay00265b
Bera K, Das AK, Nag M, Basak S (2014) Development of a rhodamine-rhodanine-based fluorescent mercury sensor and its use to monitor real-time uptake and distribution of inorganic mercury in live zebrafish larvae. Anal Chem 86:2740–2746. https://doi.org/10.1021/ac404160v
Mao Y, Hong M, Liu A, Xu D (2015) Highly selective and sensitive detection of Hg(II) from HgCl2 by a simple rhodamine-based fluorescent sensor. J Fluoresc 25:755–761. https://doi.org/10.1007/s10895-015-1564-7
Fang Y, Zhou Y, Li JY et al (2015) Naphthalimide-Rhodamine based chemosensors for colorimetric and fluorescent sensing Hg2+ through different signaling mechanisms in corresponding solvent systems. Sensors Actuators B Chem 215:350–359. https://doi.org/10.1016/j.snb.2015.03.080
Arivazhagan C, Borthakur R, Ghosh S (2015) Ferrocene and Triazole-appended rhodamine based multisignaling sensors for Hg2+ and their application in live cell imaging. Organometallics 34:1147–1155. https://doi.org/10.1021/om500948c
Li L, Fang Z (2015) A novel “turn on” glucose-based rhodamine B fluorescent chemosensor for mercury ions recognition in aqueous solution. Spectrosc Lett 48:578–585. https://doi.org/10.1080/00387010.2014.933354
Erdemir S, Kocyigit O, Malkondu S (2015) Detection of Hg2+ ion in aqueous media by new fluorometric and colorimetric sensor based on triazole-rhodamine. J Photochem Photobiol A Chem 309:15–21. https://doi.org/10.1016/j.jphotochem.2015.04.017
Hong MM, Liu AF, Xu Y, Xu DM (2016) Synthesis and properties of three novel rhodamine-based fluorescent sensors for Hg2+. Chinese Chem Lett 27:989–992. https://doi.org/10.1016/j.cclet.2016.03.027
Li D, Li CY, Li YF et al (2016) Rhodamine-based chemodosimeter for fluorescent determination of Hg2+ in 100% aqueous solution and in living cells. Anal Chim Acta 934:218–225. https://doi.org/10.1016/j.aca.2016.05.050
Chen J, Li Y, Zhong W et al (2016) A highly selective fluorescent and colorimetric chemosensor for Hg2+ based on a new rhodamine derivative. Anal Methods 8:1964–1967. https://doi.org/10.1039/c5ay03281d
Jiao Y, Zhang L, Zhou P (2016) A rhodamine B-based fluorescent sensor toward highly selective mercury (II) ions detection. Talanta 150:14–19. https://doi.org/10.1016/j.talanta.2015.11.065
Hong M, Lu X, Chen Y, Xu D (2016) A novel rhodamine-based colorimetric and fluorescent sensor for Hg2+ in water matrix and living cell. Sensors Actuators B Chem 232:28–36. https://doi.org/10.1016/j.snb.2016.03.125
Venkatesan P, Thirumalivasan N, Wu SP (2017) A rhodamine-based chemosensor with diphenylselenium for highly selective fluorescence turn-on detection of Hg2+: In vitro and in vivo. RSC Adv 7:21733–21739. https://doi.org/10.1039/c7ra02459b
Liu C, Xiao T, Wang Y et al (2017) Rhodamine based turn-on fluorescent sensor for Hg2+ and its application of microfluidic system and bioimaging. Tetrahedron 73:5189–5193. https://doi.org/10.1016/j.tet.2017.07.012
Du W, Cheng Y, Shu W et al (2017) The influences of different substituents on spectral properties of rhodamine B based chemosensors for mercury ion and application in EC109 cells. Can J Chem 95:751–757. https://doi.org/10.1139/cjc-2017-0017
Du W, Cheng Y, Shu W, Qi Z (2017) A novel rhodamine-based fluorescence chemosensor containing polyether for mercury (II) ions in aqueous solution. Quim Nova 40:733–738
Fang Y, Li X, Li JY et al (2018) Thiooxo-Rhodamine B hydrazone derivatives bearing bithiophene group as fluorescent chemosensors for detecting mercury(II) in aqueous media and living HeLa cells. Sensors Actuators B Chem 255:1182–1190. https://doi.org/10.1016/j.snb.2017.06.050
Min KS, Manivannan R, Son YA (2018) Rhodamine-fluorene based dual channel probe for the detection of Hg2+ ions and its application in digital printing. Sensors Actuators B Chem 261:545–552. https://doi.org/10.1016/j.snb.2018.01.178
Patil SK, Das D (2019) A nanomolar detection of mercury(II) ion by a chemodosimetric rhodamine-based sensor in an aqueous medium: Potential applications in real water samples and as paper strips. Spectrochim Acta - Part A Mol Biomol Spectrosc 210:44–51. https://doi.org/10.1016/j.saa.2018.11.005
Rasheed T, Nabeel F, Bilal M et al (2019) Aqueous monitoring of toxic mercury through a rhodamine-based fluorescent sensor. Math Biosci Eng 16:1861–1873. https://doi.org/10.3934/mbe.2019090
Cicekbilek F, Yilmaz B, Bayrakci M, Gezici O (2019) An application of a schiff-base type reaction in the synthesis of a new rhodamine-based Hg(II)-Sensing agent. J Fluoresc 29:1349–1358. https://doi.org/10.1007/s10895-019-02462-5
Hazra S, Bodhak C, Chowdhury S et al (2019) A novel tryptamine-appended rhodamine-based chemosensor for selective detection of Hg 2+ present in aqueous medium and its biological applications. Anal Bioanal Chem 411:1143–1157. https://doi.org/10.1007/s00216-018-1546-0
Kan C, Shao X, Song F et al (2019) Bioimaging of a fluorescence rhodamine-based probe for reversible detection of Hg (II) and its application in real water environment. Microchem J 150:104142. https://doi.org/10.1016/j.microc.2019.104142
Patil SK, Das D (2020) A novel rhodamine-based optical probe for mercury(II) ion in aqueous medium: A nanomolar detection, wide pH range and real water sample application. Spectrochim Acta - Part A Mol Biomol Spectrosc 225:117504. https://doi.org/10.1016/j.saa.2019.117504
Wang Y, Ding H, Zhu Z et al (2020) Selective rhodamine–based probe for detecting Hg2+ and its application as test strips and cell staining. J Photochem Photobiol A Chem 390:112302. https://doi.org/10.1016/j.jphotochem.2019.112302
Vanjare BD, Mahajan PG, Ryoo HI et al (2021) Novel rhodamine based chemosensor for detection of Hg2+: Nanomolar detection, real water sample analysis, and intracellular cell imaging. Sensors Actuators B Chem 330:129308. https://doi.org/10.1016/j.snb.2020.129308
Gauthama BU, Narayana B, Sarojini BK et al (2021) Colorimetric “off–on” fluorescent probe for selective detection of toxic Hg2+ based on rhodamine and its application for in-vivo bioimaging. Microchem J 166:106233. https://doi.org/10.1016/j.microc.2021.106233
Li X, Li X, Zhao H et al (2021) A novel diarylethene-rhodamine unit based chemosensor for fluorimetric and colorimetric detection of Hg2+. J Fluoresc 31:1513–1523. https://doi.org/10.1007/s10895-021-02775-4
Huang J, Xu Y, Qian X (2009) A rhodamine-based Hg 2 + sensor with high selectivity and sensitivity in aqueous solution: A NS 2 -containing receptor S CHEME 1. Representative mechanism of the chemosensor based on the RhB A rhodamine-based sensor 1 was designed and synthesized NS 2 w. JOrgChem 74:5039–5042
Singh S, Coulomb B, Boudenne JL et al (2021) Sub-ppb mercury detection in real environmental samples with an improved rhodamine-based detection system. Talanta 224:. https://doi.org/10.1016/j.talanta.2020.121909
Ding P, Wang J, Cheng J et al (2015) Three N-stabilized rhodamine-based fluorescent probes for Al3+via Al3+-promoted hydrolysis of Schiff bases. New J Chem 39:342–348. https://doi.org/10.1039/C4NJ01357C
Roy A, Mukherjee R, Dam B et al (2018) A rhodamine-based fluorescent chemosensor for Al3+: Is it possible to control the metal ion selectivity of a rhodamine-6G based chemosensor? New J Chem 42:8415–8425. https://doi.org/10.1039/c8nj01130c
Maniyazagan M, Mariadasse R, Nachiappan M et al (2018) Synthesis of rhodamine based organic nanorods for efficient chemosensor probe for Al (III) ions and its biological applications. Sensors Actuators B Chem 254:795–804. https://doi.org/10.1016/j.snb.2017.07.106
Manjunath R, Kannan P (2018) Highly selective rhodamine-based fluorescence turn-on chemosensor for Al3+ ion. Opt Mater (Amst) 79:38–44. https://doi.org/10.1016/j.optmat.2018.03.021
Gupta VK, Mergu N, Kumawat LK, Singh AK (2015) A reversible fluorescence “off-on-off” sensor for sequential detection of aluminum and acetate/fluoride ions. Talanta 144:80–89. https://doi.org/10.1016/j.talanta.2015.05.053
Sen B, Mukherjee M, Banerjee S et al (2015) A rhodamine-based “turn-on” Al3+ ion-selective reporter and the resultant complex as a secondary sensor for F- ion are applicable to living cell staining. Dalt Trans 44:8708–8717. https://doi.org/10.1039/c5dt00315f
Mabhai S, Dolai M, Dey S et al (2018) A novel chemosensor based on rhodamine and azobenzene moieties for selective detection of Al3+ ions. New J Chem 42:10191–10201. https://doi.org/10.1039/c8nj00436f
Kaur R, Saini S, Kaur N et al (2020) Rhodamine-based fluorescent probe for sequential detection of Al3+ ions and adenosine monophosphate in water. Spectrochim Acta - Part A Mol Biomol Spectrosc 225:117523. https://doi.org/10.1016/j.saa.2019.117523
Li D, Li CY, Qi HR et al (2016) Rhodamine-based chemosensor for fluorescence determination of trivalent chromium ion in living cells. Sensors Actuators B Chem 223:705–712. https://doi.org/10.1016/j.snb.2015.09.126
Li XM, Zhao RR, Yang Y et al (2017) A Rhodamine-based fluorescent sensor for chromium ions and its application in bioimaging. Chinese Chem Lett 28:1258–1261. https://doi.org/10.1016/j.cclet.2016.12.029
Sunnapu O, Kotla NG, Maddiboyina B et al (2017) Rhodamine based effective chemosensor for Chromium(III) and their application in live cell imaging. Sensors Actuators B Chem 246:761–768. https://doi.org/10.1016/j.snb.2017.02.152
Sahana S, Mishra G, Sivakumar S, Bharadwaj PK (2018) Rhodamine – Cyclohexane diamine based “turn-on” fluorescence chemosensor for Cr3+: Photophysical & confocal cell imaging studies. J Photochem Photobiol A Chem 351:42–49. https://doi.org/10.1016/j.jphotochem.2017.10.004
Goswami S, Manna A, Aich K, Paul S (2012) A simple rhodamine-based naked-eye and fluorescence “off-on” sensor for Cu(II) in aqueous solution. Chem Lett 41:1600–1602. https://doi.org/10.1246/cl.2012.1600
Guo D, Dong Z, Luo C et al (2014) A rhodamine B-based “turn-on” fluorescent sensor for detecting Cu2+ and sulfur anions in aqueous media. RSC Adv 4:5718–5725. https://doi.org/10.1039/c3ra45931d
Li X, Chen X, Zhang Y, Son YA (2014) A highly selective rhodamine based colorimetric sensor toward Cu2+. Mol Cryst Liq Cryst 599:8–15. https://doi.org/10.1080/15421406.2014.934318
Sun Z, Li H, Guo D et al (2015) A novel piperazine-bis(rhodamine-B)-based chemosensor for highly sensitive and selective naked-eye detection of Cu2+ and its application as an INHIBIT logic device. J Lumin 167:156–162. https://doi.org/10.1016/j.jlumin.2015.06.018
Li G, Tao F, Wang H et al (2015) A novel reversible colorimetric chemosensor for the detection of Cu2+ based on a water-soluble polymer containing rhodamine receptor pendants. RSC Adv 5:18983–18989. https://doi.org/10.1039/c5ra00745c
Fang Y, Zhou Y, Rui Q, Yao C (2015) Rhodamine-ferrocene conjugate chemosensor for selectively sensing Copper(II) with multisignals: chromaticity, fluorescence, and electrochemistry and its application in living cell imaging. Organometallics 34:2962–2970. https://doi.org/10.1021/acs.organomet.5b00285
Hu Y, Zhang J, Lv YZ et al (2016) A new rhodamine-based colorimetric chemosensor for naked-eye detection of Cu 2 + in aqueous solution. Spectrochim Acta - Part A Mol Biomol Spectrosc 157:164–169. https://doi.org/10.1016/j.saa.2015.12.031
Wang X, Tao J, Chen X, Yang H (2017) An ultrasensitive and selective “off-on” rhodamine-based colorimetric and fluorescent chemodosimeter for the detection of Cu2+. Sensors Actuators B Chem 244:709–716. https://doi.org/10.1016/j.snb.2017.01.040
Maji A, Lohar S, Pal S, Chattopadhyay P (2017) A new rhodamine based ‘turn-on’ Cu 2 + ion selective chemosensor in aqueous system applicable in bioimaging. J Chem Sci 129:1423–1430. https://doi.org/10.1007/s12039-017-1349-4
Park H, An KL, Naveen M et al (2018) Rhodamine-based colorimetric and fluorescent chemosensors for the detection of Cu2+ Ions and its application to bioimaging. Bull Korean Chem Soc 39:972–981. https://doi.org/10.1002/bkcs.11537
Yang LL, Tang AL, Wang PY, Yang S (2020) Switching of C-C and C-N Coupling/Cleavage for hypersensitive detection of Cu2+by a catalytically Mediated 2-Aminoimidazolyl-Tailored Six-Membered Rhodamine Probe. Org Lett 22:8234–8239. https://doi.org/10.1021/acs.orglett.0c02814
Karakuş E (2021) A rhodamine based fluorescent chemodosimeter for the selective and sensitive detection of copper (II) ions in aqueous media and living cells. J Mol Struct 1224:129037. https://doi.org/10.1016/j.molstruc.2020.129037
Yang L, Zhang X, Yang J et al (2021) A rhodamine-based chemosensor and functionalized gel ball for detecting and adsorbing copper ions. Tetrahedron 80:131893. https://doi.org/10.1016/j.tet.2020.131893
Aydin Z, Wei Y, Guo M (2012) A highly selective rhodamine based turn-on optical sensor for Fe 3+. Inorg Chem Commun 20:93–96. https://doi.org/10.1016/j.inoche.2012.02.025
Bordini J, Calandreli I, Silva GO et al (2013) A rhodamine-B-based turn-on fluorescent sensor for biological iron(III). Inorg Chem Commun 35:255–259. https://doi.org/10.1016/j.inoche.2013.06.017
Xie P, Guo F, Xia R et al (2014) A rhodamine-dansyl conjugate as a FRET based sensor for Fe3+ in the red spectral region. J Lumin 145:849–854. https://doi.org/10.1016/j.jlumin.2013.09.003
Huang J, Xu Y, Qian X (2014) Rhodamine-based fluorescent off–on sensor for Fe3+– in aqueous solution and in living cells: 8-aminoquinoline receptor and 2: 1 binding. J Chem Soc Dalt Trans 43:5983–5989. https://doi.org/10.1039/c3dt53159g
Han X, Wang DE, Chen S et al (2015) A new rhodamine-based chemosensor for turn-on fluorescent detection of Fe3+. Anal Methods 7:4231–4236. https://doi.org/10.1039/c5ay00568j
Ma S, Yang Z, She M et al (2015) Design and synthesis of functionalized rhodamine based probes for specific intracellular fluorescence imaging of Fe3+. Dye Pigment 115:120–126. https://doi.org/10.1016/j.dyepig.2014.12.014
Yan F, Zheng T, Shi D et al (2015) Rhodamine-aminopyridine based fluorescent sensors for Fe3+ in water: Synthesis, quantum chemical interpretation and living cell application. Sensors Actuators B Chem 215:598–606. https://doi.org/10.1016/j.snb.2015.03.096
Chan S, Li Q, Tse H et al (2016) A rhodamine-based “off-on” fluorescent chemosensor for selective detection of Fe3+ in aqueous media and its application in bioimaging. RSC Adv 6:74389–74393. https://doi.org/10.1039/c6ra14411j
Zhou F, Leng TH, Liu YJ et al (2017) Water-soluble rhodamine-based chemosensor for Fe3+ with high sensitivity, selectivity and anti-interference capacity and its imaging application in living cells. Dye Pigment 142:429–436. https://doi.org/10.1016/j.dyepig.2017.03.057
Xu H, Ding H, Li G et al (2017) A highly selective fluorescent chemosensor for Fe3+ based on a new diarylethene with a rhodamine 6G unit. RSC Adv 7:29827–29834. https://doi.org/10.1039/c7ra04728b
Kumar A, Kumari C, Sain D et al (2017) Synthesis of rhodamine-based chemosensor for Fe3+ selective detection with off–on mechanism and its biological application in DL-Tumor cells. ChemistrySelect 2:2969–2974. https://doi.org/10.1002/slct.201700165
Vijay N, Wu SP, Velmathi S (2019) Turn on fluorescent chemosensor containing rhodamine B fluorophore for selective sensing and in vivo fluorescent imaging of Fe3+ ions in HeLa cell line and zebrafish. J Photochem Photobiol A Chem 384:112060. https://doi.org/10.1016/j.jphotochem.2019.112060
Wang X, Li T (2020) A novel “off-on” rhodamine-based colorimetric and fluorescent chemosensor based on hydrolysis driven by aqueous medium for the detection of Fe3+. Spectrochim Acta - Part A Mol Biomol Spectrosc 229:117951. https://doi.org/10.1016/j.saa.2019.117951
Liu Y, Zhao C, Zhao X et al (2020) A selective N, N-dithenoyl-rhodamine based fluorescent probe for Fe3+ detection in aqueous and living cells. J Environ Sci (China) 90:180–188. https://doi.org/10.1016/j.jes.2019.12.005
Wang Q, Li C, Zou Y et al (2012) A highly selective fluorescence sensor for Tin (Sn4+) and its application in imaging live cells. Org Biomol Chem 10:6740–6746. https://doi.org/10.1039/c2ob25895a
Mahapatra AK, Manna SK, Maiti K et al (2014) Imino-phenolic-azodye appended rhodamine as a primary fluorescence “off-on” chemosensor for tin (Sn4+) in solution and in RAW cells and the recognition of sulphide by [AR-Sn]. RSC Adv 4:36615–36622. https://doi.org/10.1039/c4ra05729e
Yang Z, She M, Ma S et al (2017) Rhodamine based guanidinobenzimidazole functionalized fluorescent probe for tetravalent tin and its application in living cells imaging. Sensors Actuators B Chem 242:872–879. https://doi.org/10.1016/j.snb.2016.09.170
Yan Z, Wei G, Guang S et al (2018) A multidentate ligand chromophore with rhodamine-triazole-pyridine units and its acting mechanism for dual-mode visual sensing trace Sn2+. Dye Pigment 159:542–550. https://doi.org/10.1016/j.dyepig.2018.07.028
Wang X, Zhang L, Zhuang S et al (2019) A novel fluorescent sensor for Sn4+ detection: Dark resonance energy transfer from silole to rhodamine. Appl Organomet Chem 33:2–8. https://doi.org/10.1002/aoc.5067
Mahapatra AK, Manna SK, Mandal D, Das MC (2013) Highly sensitive and selective rhodamine-based “off-on” reversible chemosensor for tin (Sn4+) and imaging in living cells. Inorg Chem 52:10825–10834. https://doi.org/10.1021/ic4007026
Cheng J, Yang E, Ding P et al (2015) Two rhodamine based chemosensors for Sn4+ and the application in living cells. Sensors Actuators B Chem 221:688–693. https://doi.org/10.1016/j.snb.2015.07.003
Wechakorn K, Suksen K, Piyachaturawat P, Kongsaeree P (2016) Rhodamine-based fluorescent and colorimetric sensor for zinc and its application in bioimaging. Sensors Actuators B Chem 228:270–277. https://doi.org/10.1016/j.snb.2016.01.045
Karmegam MV, Karuppannan S, Christopher Leslee DB et al (2020) Phenothiazine–rhodamine-based colorimetric and fluorogenic ‘turn-on’’ sensor for Zn2+ and bioimaging studies in live cells’. Luminescence 35:90–97. https://doi.org/10.1002/bio.3701
Maniyazagan M, Mariadasse R, Jeyakanthan J et al (2017) Rhodamine based “turn–on” molecular switch FRET–sensor for cadmium and sulfide ions and live cell imaging study. Sensors Actuators B Chem 238:565–577. https://doi.org/10.1016/j.snb.2016.07.102
Aich K, Goswami S, Das S et al (2015) Cd2+ Triggered the FRET “ON”: A new molecular switch for the ratiometric detection of Cd2+ with live-cell imaging and bound X-ray structure. Inorg Chem 54:7309–7315. https://doi.org/10.1021/acs.inorgchem.5b00784
Kumari C, Sain D, Kumar A et al (2017) Intracellular detection of hazardous Cd2+ through a fluorescence imaging technique by using a nontoxic coumarin based sensor. Dalt Trans 46:2524–2531. https://doi.org/10.1039/c6dt04833a
Sakthivel P, Sekar K, Sivaraman G, Singaravadivel S (2017) Rhodamine diaminomaleonitrile conjugate as a novel colorimetric fluorescent sensor for recognition of Cd2+ Ion. J Fluoresc 27:1109–1115. https://doi.org/10.1007/s10895-017-2046-x
Sunnapu O, Kotla NG, Maddiboyina B et al (2015) A rhodamine based “turn-on” fluorescent probe for Pb(II) and live cell imaging. RSC Adv 6:656–660. https://doi.org/10.1039/c5ra20482h
Srisuratsiri P, Kanjanasirirat P, Chairongdua A, Kongsaeree P (2017) Reversible rhodamine-alkyne Au3+-selective chemosensor and its bioimaging application. Tetrahedron Lett 58:3194–3199. https://doi.org/10.1016/j.tetlet.2017.07.014
Wu G, Wang Z, Zhang W et al (2019) A novel rhodamine B and purine derivative-based fluorescent chemosensor for detection of palladium (II) ion. Inorg Chem Commun 102:233–239. https://doi.org/10.1016/j.inoche.2019.02.038
Tang FK, Chan SM, Wang T et al (2020) Highly selective detection of Pd2+ ion in aqueous solutions with rhodamine-based colorimetric and fluorescent chemosensors. Talanta 210:. https://doi.org/10.1016/j.talanta.2019.120634
Wang M, Liu X, Lu H et al (2015) Highly selective and reversible chemosensor for Pd2+ detected by fluorescence, colorimetry, and test paper. ACS Appl Mater Interfaces 7:1284–1289. https://doi.org/10.1021/am507479m
Chen Y, Chen B, Han Y (2016) A novel rhodamine-based fluorescent probe for the fluorogenic and chromogenic detection of Pd2+ ions and its application in live-cell imaging. Sensors Actuators B Chem 237:1–7. https://doi.org/10.1016/j.snb.2016.06.067
Mironenko AY, Tutov MV, Sergeev AA et al (2017) On/off rhodamine based fluorescent probe for detection of Au and Pd in aqueous solutions. Sensors Actuators B Chem 246:389–394. https://doi.org/10.1016/j.snb.2017.02.092
Chen H, Jin X, Zhang W et al (2018) A new rhodamine B-based ‘off-on’ colorimetric chemosensor for Pd2+ and its imaging in living cells. Inorganica Chim Acta 482:122–129. https://doi.org/10.1016/j.ica.2018.05.032
Soares-Paulino AA, Giroldo L, Pradie NA et al (2020) Nanomolar Detection of Palladium (II) through a Novel Seleno-Rhodamine-based fluorescent and colorimetric chemosensor. Dye Pigment 179:. https://doi.org/10.1016/j.dyepig.2020.108355
Pitsanuwong C, Boonwan J, Chomngam S et al (2021) A rhodamine-based fluorescent chemodosimeter for Au3+ in aqueous solution and living cells. J Fluoresc 31:1211–1218. https://doi.org/10.1007/s10895-021-02725-0
Emrullahoǧlu M, Karakuş E, Üçüncü M (2013) A rhodamine based “turn-on” chemodosimeter for monitoring gold ions in synthetic samples and living cells. Analyst 138:3638–3641. https://doi.org/10.1039/c3an00024a
Mondal S, Manna SK, Pathak S et al (2020) A “turn-on” fluorescent and colorimetric chemodosimeter for selective detection of Au3+ ions in solution and in live cells: Via Au3+-induced hydrolysis of a rhodamine-derived Schiff base. New J Chem 44:7954–7961. https://doi.org/10.1039/d0nj01273d
Liu A, Yang L, Zhang Z et al (2013) A novel rhodamine-based colorimetric and fluorescent sensor for the dual-channel detection of Cu2+ and Fe3+ in aqueous solutions. Dye Pigment 99:472–479. https://doi.org/10.1016/j.dyepig.2013.06.007
Lohar S, Banerjee A, Sahana A et al (2013) A rhodamine-naphthalene conjugate as a FRET based sensor for Cr 3+ and Fe3+ with cell staining application. Anal Methods 5:442–445. https://doi.org/10.1039/c2ay26224j
Sivaraman G, Anand T, Chellappa D (2014) A fluorescence switch for the detection of nitric oxide and histidine and its application in live cell imaging. ChemPlusChem 79:1761–1766. https://doi.org/10.1002/cplu.201402217
Chemate S, Sekar N (2015) A new rhodamine based OFF-ON fluorescent chemosensors for selective detection of Hg2+ and Al3+ in aqueous media. Sensors Actuators B Chem 220:1196–1204. https://doi.org/10.1016/j.snb.2015.06.061
Liu L, Wang A, Wang G et al (2015) A naphthopyran-rhodamine based fluorescent and colorimetric chemosensor for recognition of common trivalent metal ions and Cu2+ ions. Sensors Actuators B Chem 215:388–395. https://doi.org/10.1016/j.snb.2015.03.093
Patidar R, Rebary B, Paul P (2015) Colorimetric and fluorogenic recognition of Hg2+ and Cr3+ in acetonitrile and their test paper recognition in aqueous media with the aid of rhodamine based sensors. J Fluoresc 25:387–395. https://doi.org/10.1007/s10895-015-1524-2
Arumugaperumal R, Srinivasadesikan V, Lin MC et al (2016) Facile rhodamine-based colorimetric sensors for sequential detections of Cu(ii) ions and pyrophosphate (P2O74−) anions. RSC Adv 6:106631–106640. https://doi.org/10.1039/c6ra24472f
Weerasinghe AJ, Oyeamalu AN, Abebe FA et al (2016) Rhodamine based turn-on sensors for Ni2+ and Cr3+ in organic media: detecting CN− via the metal displacement approach. J Fluoresc 26:891–898. https://doi.org/10.1007/s10895-016-1777-4
Ozdemir M (2016) A rhodamine-based colorimetric and fluorescent probe for dual sensing of Cu2+ and Hg2+ ions. J Photochem Photobiol A Chem 318:7–13. https://doi.org/10.1016/j.jphotochem.2015.10.027
Lan T, Wang FH, Xi XJ et al (2016) A rhodamine-based dual chemosensor for the simultaneous detection of Fe3+ and Cu2+. Anal Sci 32:1223–1230. https://doi.org/10.2116/analsci.32.1223
Wang L, Ye D, Li W et al (2017) Fluorescent and colorimetric detection of Fe(III) and Cu(II) by a difunctional rhodamine-based probe. Spectrochim Acta - Part A Mol Biomol Spectrosc 183:291–297. https://doi.org/10.1016/j.saa.2017.04.056
Su W, Yuan S, Wang E (2017) A rhodamine-based fluorescent chemosensor for the detection of Pb2+, Hg2+ and Cd2+. J Fluoresc 27:1871–1875. https://doi.org/10.1007/s10895-017-2124-0
Dey S, Sarkar S, Maity D, Roy P (2017) Rhodamine based chemosensor for trivalent cations: Synthesis, spectral properties, secondary complex as sensor for arsenate and molecular logic gates. Sensors Actuators B Chem 246:518–534. https://doi.org/10.1016/j.snb.2017.02.094
Wang KP, Chen JP, Zhang SJ et al (2017) Thiophene-based rhodamine as selectivef luorescence probe for Fe(III) and Al(III) in living cells. Anal Bioanal Chem 409:5547–5554. https://doi.org/10.1007/s00216-017-0490-8
Wang Y, Chang HQ, Wu WN et al (2017) Rhodamine-2-thioxoquinazolin-4-one conjugate: A highly sensitive and selective chemosensor for Fe3+ ions and crystal structures of its Ag(I) and Hg(II) complexes. Sensors Actuators B Chem 239:60–68. https://doi.org/10.1016/j.snb.2016.07.170
Rai A, Singh AK, Tripathi K et al (2018) A quick and selective rhodamine based “smart probe” for “signal-on” optical detection of Cu2+ and Al3+ in water, cell imaging, computational studies and solid state analysis. Sensors Actuators B Chem 266:95–105. https://doi.org/10.1016/j.snb.2018.02.019
Senthil Murugan A, Vidhyalakshmi N, Ramesh U, Annaraj J (2018) In vivo bio-imaging studies of highly selective, sensitive rhodamine based fluorescent chemosensor for the detection of Cu2+/Fe3+ ions. Sensors Actuators B Chem 274:22–29. https://doi.org/10.1016/j.snb.2018.07.104
Rasheed T, Li C, Zhang Y et al (2018) Rhodamine-based multianalyte colorimetric probe with potentialities as on-site assay kit and in biological systems. Sensors Actuators B Chem 258:115–124. https://doi.org/10.1016/j.snb.2017.11.100
Roy A, Shee U, Mukherjee A et al (2019) Rhodamine-based dual chemosensor for Al 3+ and Zn 2+ ions with distinctly separated excitation and emission wavelengths. ACS Omega 4:6864–6875. https://doi.org/10.1021/acsomega.9b00475
Mironenko AY, Tutov MV, Chepak AK et al (2019) A novel rhodamine-based turn-on probe for fluorescent detection of Au 3+ and colorimetric detection of Cu 2+. Tetrahedron 75:1492–1496. https://doi.org/10.1016/j.tet.2019.01.068
Mabhai S, Dolai M, Dey SK et al (2019) Rhodamine-azobenzene based single molecular probe for multiple ions sensing: Cu 2+, Al 3+, Cr 3+ and its imaging in human lymphocyte cells. Spectrochim Acta - Part A Mol Biomol Spectrosc 219:319–332. https://doi.org/10.1016/j.saa.2019.04.056
Roy A, Das S, Sacher S et al (2019) A rhodamine based biocompatible chemosensor for Al3+, Cr3+ and Fe3+ ions: Extraordinary fluorescence enhancement and a precursor for future chemosensors. Dalt Trans 48:17594–17604. https://doi.org/10.1039/c9dt03833g
Jiang D, Xue X, Zhang G et al (2019) Simple and efficient rhodamine-derived VO2+ and Cu2+-responsive colorimetric and reversible fluorescent chemosensors toward the design of multifunctional materials. J Mater Chem C 7:3576–3589. https://doi.org/10.1039/c8tc06296j
Sağırlı A, Bozkurt E (2020) Rhodamine-based arylpropenone azo dyes as dual chemosensor for Cu2+/Fe3+ detection. J Photochem Photobiol A Chem 403:. https://doi.org/10.1016/j.jphotochem.2020.112836
Hu JP, Yang HH, Lin Q et al (2020) A rhodamine-based dual chemosensor for the naked-eye detection of Hg2+and enhancement of the fluorescence emission for Fe3+. Photochem Photobiol Sci 19:1690–1696. https://doi.org/10.1039/d0pp00302f
Sadak AE, Karakuş E (2020) Triazatruxene–rhodamine-based ratiometric fluorescent chemosensor for the sensitive, rapid detection of trivalent metal ions: Aluminium (III), Iron (III) and Chromium (III). J Fluoresc 30:213–220. https://doi.org/10.1007/s10895-020-02491-5
Chan WC, Saad HM, Sim KS et al (2021) A rhodamine based chemosensor for solvent dependent chromogenic sensing of cobalt (II) and copper (II) ions with good selectivity and sensitivity: Synthesis, filter paper test strip, DFT calculations and cytotoxicity. Spectrochim Acta - Part A Mol Biomol Spectrosc 262:120099. https://doi.org/10.1016/j.saa.2021.120099
Tavallali H, Deilamy-Rad G, Parhami A, Hasanli N (2015) An efficient and ultrasensitive rhodamine B-based reversible colorimetric chemosensor for naked-eye recognition of molybdenum and citrate ions in aqueous solution: Sensing behavior and logic operation. Spectrochim Acta - Part A Mol Biomol Spectrosc 139:253–261. https://doi.org/10.1016/j.saa.2014.11.110
Ding H, Zheng C, Li B et al (2016) A rhodamine-based sensor for Hg2+ and resultant complex as a fluorescence sensor for I-. RSC Adv 6:80723–80728. https://doi.org/10.1039/c6ra17861h
Majumdar A, Lim CS, Kim HM, Ghosh K (2017) New six-membered pH-Insensitive rhodamine spirocycle in selective sensing of Cu2+ through C-C bond cleavage and its application in cell imaging. ACS Omega 2:8167–8176. https://doi.org/10.1021/acsomega.7b01324
Yoon JW, Chang MJ, Hong S, Lee MH (2017) A fluorescent probe for copper and hypochlorite based on rhodamine hydrazide framework. Tetrahedron Lett 58:3887–3893. https://doi.org/10.1016/j.tetlet.2017.08.071
Mehta R, Kaur P, Choudhury D et al (2019) Al 3+ induced hydrolysis of rhodamine-based Schiff-base: Applications in cell imaging and ensemble as CN - sensor in 100% aqueous medium. J Photochem Photobiol A Chem 380:111851. https://doi.org/10.1016/j.jphotochem.2019.05.014
Abebe F, Gonzalez J, Makins-Dennis K, Shaw R (2020) A new bis(rhodamine)-based colorimetric chemosensor for Cu2+. Inorg Chem Commun 120:108154. https://doi.org/10.1016/j.inoche.2020.108154
Abebe F, Perkins P, Shaw R, Tadesse S (2020) A rhodamine-based fluorescent sensor for selective detection of Cu2+ in aqueous media: Synthesis and spectroscopic properties. J Mol Struct 1205:127594. https://doi.org/10.1016/j.molstruc.2019.127594
Kan C, Wu L, Wang X et al (2021) Rhodamine B-based chemiluminescence sensor for aluminum ion monitoring and bioimaging applications. Tetrahedron 85:132054. https://doi.org/10.1016/j.tet.2021.132054
Tan JL, Zhang MX, Zhang F et al (2015) A novel “off-on” colorimetric and fluorescent rhodamine-based pH chemosensor for extreme acidity. Spectrochim Acta - Part A Mol Biomol Spectrosc 140:489–494. https://doi.org/10.1016/j.saa.2014.12.110
Tan JL, Yang TT, Liu Y et al (2016) Sensitive detection of strong acidic condition by a novel rhodamine-based fluorescent pH chemosensor. Luminescence 31:865–870. https://doi.org/10.1002/bio.3043
Xue Z, Chen M, Chen J et al (2014) A rhodamine-benzimidazole based sensor for selective imaging of acidic pH. RSC Adv 4:374–378. https://doi.org/10.1039/c3ra45329d
Liu A, Hong M, Yang W et al (2014) One-pot synthesis of a new rhodamine-based dually-responsive pH sensor and its application to bioimaging. Tetrahedron 70:6974–6979. https://doi.org/10.1016/j.tet.2014.07.087
Lee D, Swamy KMK, Hong J et al (2018) A rhodamine-based fluorescent probe for the detection of lysosomal pH changes in living cells. Sensors Actuators B Chem 266:416–421. https://doi.org/10.1016/j.snb.2018.03.133
Zhang XF, Wang TR, Cao XQ, Shen SL (2020) A near-infrared rhodamine-based lysosomal pH probe and its application in lysosomal pH rise during heat shock. Spectrochim Acta - Part A Mol Biomol Spectrosc 227:117761. https://doi.org/10.1016/j.saa.2019.117761
Sunnapu O, Kotla NG, Maddiboyina B et al (2017) Rhodamine-Based Fluorescent Turn-On Probe for Facile Sensing and Imaging of ATP in Mitochondria. ChemistrySelect 2:7654–7658. https://doi.org/10.1002/slct.201701149
Chen H, Zhou B, Ye R et al (2017) Synthesis and evaluation of a new fluorescein and rhodamine B-based chemosensor for highly sensitive and selective detection of cysteine over other amino acids and its application in living cell imaging. Sensors Actuators B Chem 251:481–489. https://doi.org/10.1016/j.snb.2017.05.078
Shu H, Wu X, Zhou B et al (2017) Synthesis and evaluation of a novel fluorescent chemosensor for glutathione based on a rhodamine B and N-[4-(carbonyl) phenyl]maleimide conjugate and its application in living cell imaging. Dye Pigment 136:535–542. https://doi.org/10.1016/j.dyepig.2016.08.063
Liu Y, Lee D, Wu D et al (2018) A new kind of rhodamine-based fluorescence turn-on probe for monitoring ATP in mitochondria. Sensors Actuators B Chem 265:429–434. https://doi.org/10.1016/j.snb.2018.03.081
Tikum AF, Kim G, Nasirian A et al (2019) Rhodamine-based near-infrared probe for emission detection of ATP in lysosomes in living cells. Sensors Actuators B Chem 292:40–47. https://doi.org/10.1016/j.snb.2019.04.112
Zhang H, Li K, Li LL et al (2019) Pyridine-Si-xanthene: A novel near-infrared fluorescent platform for biological imaging. Chinese Chem Lett 30:1063–1066. https://doi.org/10.1016/j.cclet.2019.03.017
Long L, Zhang D, Li X et al (2013) A fluorescence ratiometric sensor for hypochlorite based on a novel dual-fluorophore response approach. Anal Chim Acta 775:100–105. https://doi.org/10.1016/j.aca.2013.03.016
Lee HJ, Cho MJ, Chang SK (2015) Ratiometric signaling of hypochlorite by the oxidative cleavage of sulfonhydrazide-based rhodamine-dansyl dyad. Inorg Chem 54:8644–8649. https://doi.org/10.1021/acs.inorgchem.5b01284
Ou Z, Shi L, Huang W et al (2017) A ratiometric fluorescent probe for selective detection of hypochlorite anion. Bull Korean Chem Soc 38:1443–1446. https://doi.org/10.1002/bkcs.11321
Sain D, Goswami S, Das Mukhopadhyay C (2017) Intracellular detection of toxic hypochlorite anion by using a nontoxic rhodamine based sensor. J Indian Chem Soc 94:673–680
Wu L, Shi Y, Yu H et al (2021) Bromination-induced spirocyclization of rhodamine dyes affording a FRET-based ratiometric fluorescent probe for visualization of hypobromous acid (HOBr) in live cells and zebrafish. Sensors Actuators B Chem 337:129790. https://doi.org/10.1016/j.snb.2021.129790
Zhou Z, Yuan X, Long D et al (2021) A pyridine-Si-rhodamine-based near-infrared fluorescent probe for visualizing reactive oxygen species in living cells. Spectrochim Acta - Part A Mol Biomol Spectrosc 246:118927. https://doi.org/10.1016/j.saa.2020.118927
Ambikapathi G, Kempahanumakkagari SK, Ramappa Lamani B et al (2013) Bioimaging of peroxynitrite in MCF-7 Cells by a new fluorescent probe rhodamine b phenyl hydrazide. J Fluoresc 23:705–712. https://doi.org/10.1007/s10895-013-1205-y
Peng T, Chen X, Gao L et al (2016) A rationally designed rhodamine-based fluorescent probe for molecular imaging of peroxynitrite in live cells and tissues. Chem Sci 7:5407–5413. https://doi.org/10.1039/c6sc00012f
Miao J, Huo Y, Shi H et al (2018) A Si-rhodamine-based near-infrared fluorescent probe for visualizing endogenous peroxynitrite in living cells, tissues, and animals. J Mater Chem B 6:4466–4473. https://doi.org/10.1039/c8tb00987b
Zhang X, Chen Y, Liu C et al (2019) A novel hexahydropyridazin-modified rhodamine fluorescent probe for tracing endogenous/exogenous peroxynitrite in live cells and zebrafish. Dye Pigment 170:107573. https://doi.org/10.1016/j.dyepig.2019.107573
Mao GJ, Gao GQ, Dong WP et al (2021) A two-photon excited near-infrared fluorescent probe for imaging peroxynitrite during drug-induced hepatotoxicity and its remediation. Talanta 221:. https://doi.org/10.1016/j.talanta.2020.121607
Xia Q, Feng S, Hong J, Feng G (2021) One probe for multiple targets: A NIR fluorescent rhodamine-based probe for ONOO− and lysosomal pH detection in live cells. Sensors Actuators B Chem 337:129732. https://doi.org/10.1016/j.snb.2021.129732
Yu H, Jin L, Dai Y et al (2013) From a BODIPY-rhodamine scaffold to a ratiometric fluorescent probe for nitric oxide. New J Chem 37:1688–1691. https://doi.org/10.1039/c3nj41127c
Meng Q, Zhang Y, Hou D et al (2013) Fluorimetric and colorimetric detection of nitric oxide in living cells by rhodamine derivatives assisted by Cu2+. Tetrahedron 69:636–641. https://doi.org/10.1016/j.tet.2012.11.010
Huo Y, Miao J, Han L et al (2017) Selective and sensitive visualization of endogenous nitric oxide in living cells and animals by a Si-rhodamine deoxylactam-based near-infrared fluorescent probe. Chem Sci 8:6857–6864
Mao Z, Jiang H, Song X et al (2017) Development of a silicon-rhodamine based near-infrared emissive two-photon fluorescent probe for nitric oxide. Anal Chem 89:9620–9624. https://doi.org/10.1021/acs.analchem.7b02697
Wang Q, Jiao X, Liu C et al (2018) A rhodamine-based fast and selective fluorescent probe for monitoring exogenous and endogenous nitric oxide in live cells. J Mater Chem B 6:4096–4103. https://doi.org/10.1039/c8tb00646f
Alam R, Islam ASM, Sasmal M et al (2018) A rhodamine-based turn-on nitric oxide sensor in aqueous medium with endogenous cell imaging: An unusual formation of nitrosohydroxylamine. Org Biomol Chem 16:3910–3920. https://doi.org/10.1039/c8ob00822a
Jiang WL, Li Y, Liu HW et al (2019) A rhodamine-deoxylactam based fluorescent probe for fast and selective detection of nitric oxide in living cells. Talanta 197:436–443. https://doi.org/10.1016/j.talanta.2019.01.061
Tavallali H, Deilamy-Rad G, Parhami A, Hasanli N (2014) A novel cyanide-selective colorimetric and fluorescent chemosensor: First molecular security keypad lock based on phosphotungstic acid and CN- inputs. J Hazard Mater 266:189–197. https://doi.org/10.1016/j.jhazmat.2013.12.026
Pei PX, Hu JH, Ni PW et al (2017) A novel dual-channel chemosensor for CN- based on rhodamine B hydrazide derivatives and its application in bitter almondf. RSC Adv 7:46832–46838. https://doi.org/10.1039/c7ra09174e
Mehta R, Luxami V (2020) A Novel ‘On-Off’ rhodamine based sensor for colorimetric detection of CN−and its application as encoder-decoder and molecular keypad lock. ChemistrySelect 5:13429–13438. https://doi.org/10.1002/slct.202002987
Sivaraman G, Chellappa D (2013) Rhodamine based sensor for naked-eye detection and live cell imaging of fluoride ions. J Mater Chem B 1:5768–5772. https://doi.org/10.1039/C3TB21041C
Mandal S, Sahana A, Banerjee A et al (2015) A smart rhodamine-pyridine conjugate for bioimaging of thiocyanate in living cells. RSC Adv 5:103350–103357. https://doi.org/10.1039/c5ra21838a
Roy S, Maity A, Mudi N et al (2019) Rhodamine scaffolds as real time chemosensors for selective detection of bisulfite in aqueous medium. Photochem Photobiol Sci 18:1342–1349. https://doi.org/10.1039/c8pp00558c
Wu WH, Dong JJ, Wang X et al (2012) Fluorogenic and chromogenic probe for rapid detection of a nerve agent simulant DCP. Analyst 137:3224–3226. https://doi.org/10.1039/c2an35428d
Wu Z, Wu X, Yang Y et al (2012) A rhodamine-deoxylactam based sensor for chromo-fluorogenic detection of nerve agent simulant. Bioorganic Med Chem Lett 22:6358–6361. https://doi.org/10.1016/j.bmcl.2012.08.077
Georgiev NI, Bojinov VB, Venkova AI (2013) Design, synthesis and pH sensing properties of novel PAMAM light-harvesting dendrons based on rhodamine 6G and 1,8-naphthalimide. J Fluoresc 23:459–471. https://doi.org/10.1007/s10895-013-1168-z
Said AI, Georgiev NI, Bojinov VB (2022) A novel dual naked eye colorimetric and fluorescent pH chemosensor and its ability to execute three INHIBIT based digital comparator. Dye Pigment 205:110489. https://doi.org/10.1016/j.dyepig.2022.110489
Georgiev NI, Asiri AM, Qusti AH et al (2014) A pH sensitive and selective ratiometric PAMAM wavelength-shifting bichromophoric system based on PET, FRET and ICT. Dye Pigment 102:35–45. https://doi.org/10.1016/j.dyepig.2013.10.007
Georgiev NI, Asiri AM, Alamry KA et al (2014) Selective ratiometric pH-sensing PAMAM light-harvesting dendrimer based on Rhodamine 6G and 1,8-naphthalimide. J Photochem Photobiol A Chem 277:62–74. https://doi.org/10.1016/j.jphotochem.2013.12.005
Alamry KA, Georgiev NI, El-Daly SA et al (2015) A highly selective ratiometric fluorescent pH probe based on a PAMAM wavelength-shifting bichromophoric system. Spectrochim Acta - Part A Mol Biomol Spectrosc 135:792–800. https://doi.org/10.1016/j.saa.2014.07.076
Alamry KA, Georgiev NI, El-Daly SA et al (2015) A ratiometric rhodamine-naphthalimide pH selective probe built on the basis of a PAMAM light-harvesting architecture. J Lumin 158:50–59. https://doi.org/10.1016/j.jlumin.2014.09.014
Georgiev NI, Dimitrova MD, Asiri AM et al (2015) Synthesis, sensor activity and logic behaviour of a novel bichromophoric system based on rhodamine 6G and 1,8-naphthalimide. Dye Pigment 115:172–180. https://doi.org/10.1016/j.dyepig.2015.01.001
Dimitrova MD, Georgiev NI, Bojinov VB (2016) Novel PAMAM dendron as a bichromophoric probe based on rhodamine 6G and 1,8-naphthalimide. J Fluoresc 26:1091–1100. https://doi.org/10.1007/s10895-016-1799-y
Said AI, Georgiev NI, Bojinov VB (2019) A smart chemosensor: Discriminative multidetection and various logic operations in aqueous solution at biological pH. Spectrochim Acta - Part A Mol Biomol Spectrosc 223:117304. https://doi.org/10.1016/j.saa.2019.117304
Said AI, Georgiev NI, Hamdan SA, Bojinov VB (2019) A chemosensoring molecular lab for various analytes and its ability to execute a molecular logical digital comparator. J Fluoresc 29:1431–1443. https://doi.org/10.1007/s10895-019-02464-3
Li L, Dong X, Li J, Wei J (2020) A short review on NIR-II organic small molecule dyes. Dye Pigment 183:. https://doi.org/10.1016/j.dyepig.2020.108756
Luo S, Zhang E, Su Y et al (2011) A review of NIR dyes in cancer targeting and imaging. Biomaterials 32:7127–7138. https://doi.org/10.1016/j.biomaterials.2011.06.024
Lang W, Cheng G, Peng R, Cao QY (2021) Rhodamine-anchored poly(norbornene) for fluorescent sensing of ATP. Dye Pigment 189:. https://doi.org/10.1016/j.dyepig.2021.109245
Li M, Zhang S, Zhang P et al (2022) Rhodamine functionalized cellulose for mercury detection and removal: A strategy for providing in situ fluorimetric and colorimetric responses. Chem Eng J 436:. https://doi.org/10.1016/j.cej.2022.135251
Lang W, Zhou F, Chen Y, Cao QY (2022) A new poly(norbornene)-based sensor for fluorescent ratiometric sensing of adenosine 5′-triphosphate. Dye Pigment 200:110187. https://doi.org/10.1016/j.dyepig.2022.110187
Acknowledgements
Financial assistance provided by Council of Industrial and Scientific Research – HRDG, in the form of Junior Research Fellowship is greatly acknowledged by one of the authors (R. Lalitha).
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The authors Raguraman Lalitha acknowledges the CSIR-HRDG (Council of Scientific and Industrial Research-India) Fellowship scheme for financial support and authors acknowledge the director of National Institute of Technology-Trichy for providing research infrastructure.
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Lalitha, R., Velmathi, S. A Study of Small Molecule-Based Rhodamine-Derived Chemosensors and their Implications in Environmental and Biological Systems from 2012 to 2021: Latest Advancement and Future Prospects. J Fluoresc 34, 15–118 (2024). https://doi.org/10.1007/s10895-023-03231-1
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DOI: https://doi.org/10.1007/s10895-023-03231-1