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Phosphorus–nitrogen compounds: part 30. Syntheses and structural investigations, antimicrobial and cytotoxic activities and DNA interactions of vanillinato-substituted NN or NO spirocyclic monoferrocenyl cyclotriphosphazenes
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1 of the 40 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1002/ardp.201100412 (notice 2013-04-02).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-4555(199804)29:4<327::aid-jrs245>3.0.co;2-5openalex-snapshot
Infrared and Raman spectra of the phosphazene high polymer [NP(O2C12H8)]n
inferredcites →https://doi.org/10.1002/9780470478882openalex-snapshot
Polyphosphazenes for Biomedical Applications
inferredcites →https://doi.org/10.1002/ardp.201100412openalex-snapshot
Synthesis, Characterization, and Biological–Pharmacological Evaluation of New Phosphazenes Bearing Dioxybiphenyl and Schiff Base Groups
inferredcites →https://doi.org/10.1002/chem.201202748openalex-snapshot
New Liquid Crystalline Materials Based on Two Generations of Dendronised Cyclophosphazenes
inferredcites →https://doi.org/10.1002/ejic.200901198openalex-snapshot
The Nature of the Phosphazene Nitrogen–Metal Bond: DFT Calculations on 2‐(Pyridyloxy)cyclophosphazene Complexes
inferredcites →https://doi.org/10.1002/hc.21139openalex-snapshot
Syntheses of Chiral Phosphazenes with Stereogenic Centers: NMR Behavior in the Presence of a Chiral Solvating Agent
inferredcites →https://doi.org/10.1007/978-1-4684-1521-6_9openalex-snapshot
Nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1007/s00280-013-2156-3openalex-snapshot
Preventing the autophagic survival response by inhibition of calpain enhances the cytotoxic activity of bortezomib in vitro and in vivo
inferredcites →https://doi.org/10.1007/s00775-011-0869-5openalex-snapshot
Cellular accumulation and DNA interaction studies of cytotoxic trans-platinum anticancer compounds
inferredcites →https://doi.org/10.1007/s10847-009-9578-xopenalex-snapshot
Phosphorus–nitrogen compounds: part 16. Synthesis, stereogenism, anisochronism and the relationship between 31P NMR spectral and crystallographic data of monotopic spiro-crypta phosphazene derivatives
inferredcites →https://doi.org/10.1007/s11164-012-0670-2openalex-snapshot
Synthesis, characterization, and biological evaluation of new oxime-phosphazenes
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/j.biomaterials.2004.02.016openalex-snapshot
Low temperature formation of hydroxyapatite-poly(alkyl oxybenzoate)phosphazene composites for biomedical applications
inferredcites →https://doi.org/10.1016/j.ejmech.2012.03.018openalex-snapshot
Synthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agents
inferredcites →https://doi.org/10.1016/j.ica.2013.03.001openalex-snapshot
Phosphorus–nitrogen compounds: Part 26. Syntheses, spectroscopic and structural investigations, biological and cytotoxic activities, and DNA interactions of mono and bisferrocenylspirocyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.molstruc.2013.06.036openalex-snapshot
Phosphorus–nitrogen compounds: Part 28. Syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of new phosphazenes bearing vanillinato and pendant ferrocenyl groups
inferredcites →https://doi.org/10.1016/j.poly.2007.09.026openalex-snapshot
Synthesis, structure and metallation of spiro-N3P3(O2C12H8)(OC5H4N-2)4: A heptacoordinate Co(II) in the molecular structure of N3P3(O2C12H8)(OC5H4N-2)4·Co(NO3)2
inferredcites →https://doi.org/10.1016/j.poly.2008.04.001openalex-snapshot
The synthesis and characterization of new aminoadamantane derivatives of hexachloro-cyclo-triphosphazene
inferredcites →https://doi.org/10.1016/j.poly.2010.07.017openalex-snapshot
Phosphorus–nitrogen compounds: Part 19. Syntheses, structural and electrochemical investigations, biological activities, and DNA interactions of new spirocyclic monoferrocenylcyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2013.06.050openalex-snapshot
Cyclotriphosphazene derivatives with three different chiral centres: Synthesis, characterization and investigation of their stereogenic properties
inferredcites →https://doi.org/10.1016/j.poly.2013.12.041openalex-snapshot
Cyclotriphosphazenes having stereogenic phosphorus atoms: Synthesis, characterization and their stereogenic properties
inferredcites →https://doi.org/10.1016/s0020-1693(00)84318-2openalex-snapshot
Covalent binding of non-effective diaziridinocyclotriphosphazenes to natural polyamines as tumor finders makes potential anticancer agents
inferredcites →https://doi.org/10.1016/s0020-1693(01)00557-6openalex-snapshot
AIDS-related lymphoma screen results and molecular structure determination of a new crown ether bearing aziridinylcyclophosphazene, potentially capable of ion-regulated DNA cleavage action
inferredcites →https://doi.org/10.1016/s0022-328x(99)00304-6openalex-snapshot
Synthesis of organometallic amines and their coupling to the C-terminus of amino acids and peptides
inferredcites →https://doi.org/10.1016/s0898-8838(02)53005-1openalex-snapshot
Advances in the chemistry of chlorocyclophosphazenes
inferredcites →https://doi.org/10.1021/cr00002a002openalex-snapshot
Regio- and stereochemical control in substitution reactions of cyclophosphazenes
inferredcites →https://doi.org/10.1021/ic020264hopenalex-snapshot
Diastereoisomeric Singly Bridged Cyclophosphazene-Macrocyclic Compounds
inferredcites →https://doi.org/10.1021/ic0511266openalex-snapshot
Revisiting the Electronic Structure of Phosphazenes
inferredcites →https://doi.org/10.1021/ic100781vopenalex-snapshot
Phosphorus−Nitrogen Compounds. 21. Syntheses, Structural Investigations, Biological Activities, and DNA Interactions of New N/O Spirocyclic Phosphazene Derivatives. The NMR Behaviors of Chiral Phosphazenes with Stereogenic Centers upon the Addition of Chiral Solvating Agents
inferredcites →https://doi.org/10.1021/ic701241vopenalex-snapshot
Conformationally Rigid Chelate Rings in Metal Complexes of Pyridyloxy-Substituted 2,2‘-Dioxybiphenyl-Cyclotetra- and Cyclotriphosphazene Platforms
inferredcites →https://doi.org/10.1021/ic901039kopenalex-snapshot
Phosphorus−Nitrogen Compounds. 18. Syntheses, Stereogenic Properties, Structural and Electrochemical Investigations, Biological Activities, and DNA Interactions of New Spirocyclic Mono- and Bisferrocenylphosphazene Derivatives
inferredcites →https://doi.org/10.1021/ja00839a011openalex-snapshot
General definition of ring puckering coordinates
inferredcites →https://doi.org/10.1021/ja028871ropenalex-snapshot
Anomalous NMR Behavior of Meso Compounds with Remote Stereogenic Centers on Addition of Chiral Shift Reagent or Chiral Solvating Agent
inferredcites →https://doi.org/10.1021/jm0490078openalex-snapshot
Synthesis and in Vitro Antileukemic Activity of Some New 1,3-(Oxytetraethylenoxy)cyclotriphosphazene Derivatives
inferredcites →https://doi.org/10.1039/9781847554857-00001openalex-snapshot
Nuclear magnetic resonance spectroscopy
inferredcites →https://doi.org/10.1039/j19710001450openalex-snapshot
An improved determination of the crystal structure of hexachlorocyclotriphosphazene (phosphonitrilic chloride)
inferredcites →https://doi.org/10.1039/p298700000s1openalex-snapshot
Tables of bond lengths determined by X-ray and neutron diffraction. Part 1. Bond lengths in organic compounds
inferredcites →https://doi.org/10.1080/10426507.2010.496120openalex-snapshot
Synthesis and Characterization of Side Group–Modified Cyclotetraphosphazene Derivatives
inferredcites →https://doi.org/10.1080/10426507.2013.779273openalex-snapshot
Phosphorus-Nitrogen Compounds: Part 25. Syntheses, Spectroscopic, Structural and Electrochemical Investigations, Antimicrobial Activities, and DNA Interactions of Ferrocenyldiaminocyclotriphosphazenes
inferredcites →https://doi.org/10.1107/s0021889897003117openalex-snapshot
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4816439openalex-extracted
Cyclotriphosphazenes: Pre-Harvest Foliar Applications Improve Antioxidant Activity by Increasing Phenolic Compounds in Lavandula Angustifolia Mill
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Phosphorus‐nitrogen compounds. Part 39. Syntheses and Langmuir‐Blodgett thin films and antimicrobial activities of N/N and N/O spirocyclotriphosphazenes with monoferrocenyl pendant arm
inferred← citeshttps://doi.org/10.1002/aoc.6150openalex-snapshot
The comparative reactions of 2‐cis‐4‐ansa and spiro cyclotetraphosphazenes with difunctional ligands: Structural and stereogenic properties, electrochemical, antimicrobial and cytotoxic activity studies
inferred← citeshttps://doi.org/10.1002/jccs.202100475openalex-snapshot
Phosphorus‐nitrogen compounds part 59. The syntheses of tetrachloro and tetraamino‐2‐pyridylmethylspiro(N/N)ethylenediaminocyclotriphosphazenes: Structural characterization, bioactivity, and molecular docking studies
inferred← citeshttps://doi.org/10.1002/slct.202101668openalex-snapshot
Effect of the Hydrophilic/Hydrophobic Pendants on Physicochemical Properties: Applications Based on Cyclotriphosphazene Core
inferred← citeshttps://doi.org/10.1002/slct.74742openalex-snapshot
Synthesis, Structural Analyses, Antimicrobial Activities, DNA Topoisomerase Inhibition, Cytotoxicity, and Genotoxicity Studies of Unsymmetrical Dispiro( N/N )Cyclotriphosphazenes
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Phosphorus–nitrogen compounds: part 53—synthesis, characterization, cytotoxic and antimicrobial activity, DNA interaction and molecular docking studies of new mono- and dispirocyclotriphosphazenes with pendant arm(s)
inferred← citeshttps://doi.org/10.1007/s11164-015-2271-3openalex-snapshot
Phosphorus–nitrogen compounds part 33: in vitro cytotoxic and antimicrobial activities, DNA interactions, syntheses, and structural investigations of new mono(4-nitrobenzyl)spirocyclotriphosphazenes
inferred← citeshttps://doi.org/10.1007/s11164-021-04505-8openalex-snapshot
Phosphorus–nitrogen compounds Part 55. Syntheses of 4-methoxybenzylspiro(N/N)cyclotriphosphazenes: chemical, structural and biological properties
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Phosphorus-nitrogen compounds. Part 78. Design, synthesis, crystallographic and spectral properties, free radical scavenging and bioactivity studies of tetrakis(alkylamino)monoferrocenyl-(N/N)-spiro-cyclotriphosphazenes
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Novel Waterborne P–N Polyurethane and Its Application in Leather Finishing for Flame-Retardant and Antimicrobial Properties
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Compounds Containing a Spiro Phosphorus Atom
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Cyclotriphosphazenes: Pre-harvest foliar applications improve antioxidant activity by increasing phenolic compounds in Lavandula angustifolia Mill.
inferred← citeshttps://doi.org/10.1016/j.ica.2016.02.060openalex-snapshot
Phosphorus nitrogen compounds: Part 34. Syntheses, structural investigations, cytotoxic and biological activities of spiro-ansa-spiro and spiro-bino-spiro tetrameric phosphazene derivatives
inferred← citeshttps://doi.org/10.1016/j.ica.2020.119679openalex-snapshot
Synthesis, characterization and antimicrobial properties of cyclotriphosphazenes bearing benzimidazolyl rings
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Phosphorus-nitrogen compounds: Part 61. The novel sodium complexes of monoferrocenylspirocyclotriphosphaza-crown ethers
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Phosphorus-nitrogen compounds: Part 87. Unsymmetrical dichlorobis(ferrocenylspiro)cyclotriphosphazenes: Synthesis, structural characterizations, electrochemical behavior and dye-sensitized solar cell studies
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2017.10.025openalex-snapshot
Phosphorus-nitrogen compounds. part 38. Syntheses, characterizations, cytotoxic, antituberculosis and antimicrobial activities and DNA interactions of spirocyclotetraphosphazenes with bis-ferrocenyl pendant arms
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2026.117094openalex-snapshot
Phosphorus‑nitrogen compounds: part 83. Molecular design, synthesis, and characterization of unsymmetrical Dispirocyclotriphosphazenes bearing Ferrocenyl and Carbazolylspiro (N/N) rings: Chirality, bioactivity, photophysical, dye-sensitized solar cell and memory function studies
inferred← citeshttps://doi.org/10.1016/j.molliq.2017.01.067openalex-snapshot
Synthesis, structural and thermal properties of the hexapyrrolidinocyclotriphosphazenes-based protic molten salts: Antiproliferative effects against HT29, HeLa, and C6 cancer cell lines
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.07.050openalex-snapshot
Phosphorus-nitrogen compounds: Part 43. Syntheses, spectroscopic characterizations and antimicrobial activities of cis- and trans-N/O dispirocyclotriphosphazenes containing ferrocenyl pendant arms
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.12.090openalex-snapshot
Phosphorus-nitrogen compounds: Part 45. Vanillinato-substituted cis- and trans-bisferrocenyldispirocyclotriphosphazenes: Syntheses, spectroscopic and crystallographic characterizations
inferred← citeshttps://doi.org/10.1016/j.molstruc.2019.127079openalex-snapshot
Spectroscopic, crystallographic and thermal characterizations of monospiro(N/N)cyclotriphosphazenes with 9-ethyl-3-carbazolyl pendant arm
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Reinvestigations of the reactions of hexachlorocyclotriphosphazene with difunctional primary amines leading to novel dangler, ansa and bridged derivatives. Spectroscopic studies of the derived products
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.127896openalex-snapshot
Investigation of hexakis[2-formylphenoxy]cyclotriphosphazene structure by single crystal X-ray diffraction and computer simulation
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Phosphorus-nitrogen compounds: Part 79. Design and synthesis of spiro-bino-spiro (sbs)-bis (tetraalkylaminocyclotriphosphazenes) and novel twenty-membered bis(dichlorocyclotriphos-phaza)macrocycles: Structural analysis, chirality and bioactivity studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145492openalex-snapshot
Phosphorus-nitrogen compounds. Synthesis and structural characterization of unsymmetrically substituted ferrocenylspirocyclotriphosphazenes bearing one chiral centre
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Cyclotriphosphazene based materials: Structure, functionalization and applications
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Stereochemical aspects of cyclotriphosphazenes: Prochiral and pseudo-asymmetric phosphorus atoms
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Dual-action Ag/ZnO-Polyacrylate nano-emulsion for enhanced lubrication and antimicrobial finishing of tanned leather
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inferred← citeshttps://doi.org/10.1039/c6nj00204hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/c7nj00478hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d0nj02723eopenalex-snapshot
Synthesis of the first 2-hydroxyanthraquinone substituted cyclotriphosphazenes and their cytotoxic properties
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inferred← citeshttps://doi.org/10.1080/10426507.2016.1225058openalex-snapshot
The reaction of hexachlorocyclotriphosphazatriene with P-aminophenol
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Synthesis, structural and thermal characterizations and in vitro cytotoxic activities of new cyclotriphosphazene derivatives
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The reactions of 2-trans-6-bis(4-fluorobenzyl)spirocyclotetraphosphazene with primary amines: spectroscopic and crystallographic characterizations
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The reactions of hexachlorocyclotriphosphazene with piperidine, N-(1-naphthyl)ethylenediamine and 2-(2-hydroxyethylamino)ethanol. Antimicrobial activities of iminodiethoxy-substituted cyclotriphosphazene derivatives
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Vanillinato-Substituted Monospirocyclotriphosphazenes: Synthesis, Spectroscopic and Crystallographic Characterizations, and Thermal Properties
inferred← citeshttps://doi.org/10.12991/jrp.2018.95openalex-snapshot
Synthesis and antimicrobial effects of cyclotriphosphazenes containing monocarbonyl curcumin analogs
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THE SYNTHESES AND STRUCTURAL CHARACTERIZATIONS, ANTIMICROBIAL ACTIVITY AND IN VITRO DNA BINDING OF 4-FLUOROBENZYLSPIRO(N/O)CYCLOTRIPHOSPHAZENES AND THEIR PHOSPHAZENIUM SALTS
inferred← citeshttps://doi.org/10.18596/jotcsa.287330openalex-snapshot
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inferred← citeshttps://doi.org/10.18596/jotcsa.540169openalex-snapshot
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Diamino-sübstitüe Halkalı Trifosfazen Türevlerinin Antimikrobiyal Aktivitelerinin Araştırılması
inferred← citeshttps://doi.org/10.3906/kim-1909-83openalex-snapshot
Phosphorus-nitrogen compounds- (Part 50): correlations between structuralparameters for cylophosphazene derivatives containing ferrocenyl pendant arm(s)
inferred← citeshttps://doi.org/10.3906/kim-1911-43openalex-snapshot
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New and Practical Applications of Functionalized Cyclotriphosphazene Core-Based Materials
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