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Phosphorus–nitrogen compounds: part 68. Synthesis, characterization, stereogenism, photophysical and bioactivity studies of novel unsymmetrical dispiro( N / N )cyclotriphosphazenes with carbazolyl and 4-chlorobenzyl pendant arms

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/aoc.4223openalex-snapshot
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Inhibition of Human Topoisomerase II by N,N,N‐Trimethylethanammonium Iodide Alkylcarbazole Derivatives
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Syntheses of Chiral Phosphazenes with Stereogenic Centers: NMR Behavior in the Presence of a Chiral Solvating Agent
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New Trimethoxybenzamides and Trimethoxyphenylureas Derived from Dimethylcarbazole as Cytotoxic Agents. Part I
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Solution processable high band gap hosts based on carbazole functionalized cyclic phosphazene cores for application in organic light‐emitting diodes
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Phosphorus–nitrogen compounds
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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)
inferredcites →https://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
inferredcites →https://doi.org/10.1007/s11164-022-04746-1openalex-snapshot
Phosphorus-nitrogen compounds: part 57—Syntheses of tetrachloro- and tetraaminobenzylspiro(N/N)cyclotriphosphazenes: chemical, structural characterizations, bioactivity and molecular docking studies
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The influence of the negative hyperconjugation is relevant for the analysis of the π-π* conjugation with the mono-substitution and di-substitution of H2C= by O= and/or HN= in trans-buta-1,3-diene?
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Hexa-substituted cyclotriphosphazene derivatives containing hetero-ring chalcones: Synthesis, in vitro cytotoxic activity and their DNA damage determination
inferredcites →https://doi.org/10.1016/j.bios.2022.114612openalex-snapshot
Hexa-BODIPY-cyclotriphosphazene based nanoparticle for NIR fluorescence/photoacoustic dual-modal imaging and photothermal cancer therapy
inferredcites →https://doi.org/10.1016/j.bmc.2017.11.044openalex-snapshot
Studies on interactions of carbazole derivatives with DNA, cell image, and cytotoxicity
inferredcites →https://doi.org/10.1016/j.ccr.2015.01.012openalex-snapshot
Chiral configurations in cyclophosphazene chemistry
inferredcites →https://doi.org/10.1016/j.ccr.2021.214326openalex-snapshot
Specific recognitions of multivalent cyclotriphosphazene derivatives in sensing, imaging, theranostics, and biomimetic catalysis
inferredcites →https://doi.org/10.1016/j.cej.2022.138385openalex-snapshot
Cyclotriphosphazene-based flame-retardant polymer electrolytes for high performance sodium metal batteries
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.eurpolymj.2019.08.025openalex-snapshot
Magnetic poly(cyclotriphosphazene-co-4,4′-sulfonyldiphenol) nanotubes modified with glacial acetic acid for removing methylene blue: Adsorption performance and mechanism
inferredcites →https://doi.org/10.1016/j.ica.2016.12.013openalex-snapshot
Synthesis and spectral properties of fluorene substituted cyclic and polymeric phosphazenes
inferredcites →https://doi.org/10.1016/j.ica.2018.01.016openalex-snapshot
spiro-Cyclotriphosphazenes containing 4-hydroxyphenylethyl pendant arm: Syntheses, structural characterization and DNA interaction study
inferredcites →https://doi.org/10.1016/j.ica.2019.05.048openalex-snapshot
Phosphorus-nitrogen compounds: Part 46. The reactions of N3P3Cl6 with bidentate and monodentate ligands: The syntheses, structural characterizations, antimicrobial and cytotoxic activities, and DNA interactions of (N/N)spirocyclotriphosphazenes with 4-chlorobenzyl pendant arm
inferredcites →https://doi.org/10.1016/j.ica.2019.119386openalex-snapshot
Cyclotriphosphazene cored naphthalimide-BODIPY dendrimeric systems: Synthesis, photophysical and antimicrobial properties
inferredcites →https://doi.org/10.1016/j.ica.2021.120317openalex-snapshot
Regional selectivity of 1,2-ethanediol in the reactions with cyclotriphosphazene derivatives bearing mono-amino groups
inferredcites →https://doi.org/10.1016/j.ica.2022.121022openalex-snapshot
New design of cyclotriphosphazene derivatives bearing carbazole units: The syntheses, characterization, and photophysical properties
inferredcites →https://doi.org/10.1016/j.memsci.2019.117371openalex-snapshot
Preparation and characterization of antibacterial polyamine-based cyclophosphazene nanofiltration membranes
inferredcites →https://doi.org/10.1016/j.molstruc.2005.02.015openalex-snapshot
Phosphorus–nitrogen compounds: novel spiro-cyclophosphazenic lariat (PNP-pivot) ether derivatives. Structures of 4,4,6,6-tetrachloro-2,2-[3-oxa-1,5-pentane dioxy bis(2-phenylamino)]cyclo-2λ5,4λ5,6λ5-triphosphazene and 4,4,6,6-tetrachloro-2,2-[1,2-xylylene dioxy…
inferredcites →https://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
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.molstruc.2019.02.013openalex-snapshot
Synthesis and characterization of 1,4-phenylenediamine derivatives containing hydroxyl and cyclotriphosphazene as terminal group
inferredcites →https://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
inferredcites →https://doi.org/10.1016/j.molstruc.2022.133866openalex-snapshot
Phosphorus-nitrogen compounds: Part 66. Syntheses, structural and chiral properties of multiheterocyclic cis and trans bis (benzylspiro-N/N) cyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2003.12.024openalex-snapshot
Synthesis and structures of unsymmetrical bis- and tris-cyclotriphosphazenes
inferredcites →https://doi.org/10.1016/j.poly.2011.03.028openalex-snapshot
The investigation of stereogenic properties of cyclotriphosphazene derivatives with two different chiral centres
inferredcites →https://doi.org/10.1016/j.poly.2012.06.014openalex-snapshot
Investigation of a spiro to ansa rearrangement with di-functional alcohols in cyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1016/j.poly.2013.09.011openalex-snapshot
Synthesis of a dendrimeric phenoxy-substituted cyclotetraphosphazene and its non-covalent interactions with multiwalled carbon nanotubes
inferredcites →https://doi.org/10.1016/j.triboint.2015.04.018openalex-snapshot
Highly thermally stable cyclotriphosphazene based perfluoropolyether lubricant oil
inferredcites →https://doi.org/10.1016/s0022-2860(99)00098-8openalex-snapshot
Phosphorus–nitrogen compounds: Part IV. New podand and lariat ether-type macrocycles with cyclophosphazenes. Structure of 2,2′-[triethyleneglycolbis(phenylether-2-amino)]-2,2′,4,4,4′,4′,6,6,6′,6′-decachlorobicyclo-2λ5, 2′λ5, 4λ5, 4′λ5, 6λ5, 6′λ5-triphosphazatriene
inferredcites →https://doi.org/10.1021/acs.inorgchem.9b03334openalex-snapshot
(Amino)cyclophosphazenes as Multisite Ligands for the Synthesis of Antitumoral and Antibacterial Silver(I) Complexes
inferredcites →https://doi.org/10.1021/acsomega.2c01573openalex-snapshot
Phosphazene Cyclomatrix Network-Based Polymer: Chemistry, Synthesis, and Applications
inferredcites →https://doi.org/10.1021/ed076p1260openalex-snapshot
Are Fluorescence Quantum Yields So Tricky to Measure? A Demonstration Using Familiar Stationery Products
inferredcites →https://doi.org/10.1021/ic0511266openalex-snapshot
Revisiting the Electronic Structure of Phosphazenes
inferredcites →https://doi.org/10.1021/ic3017134openalex-snapshot
Phosphorus–Nitrogen Compounds. Part 24. Syntheses, Crystal Structures, Spectroscopic and Stereogenic Properties, Biological Activities, and DNA Interactions of Novel Spiro-ansa-spiro- and Ansa-spiro-ansa-cyclotetraphosphazenes
inferredcites →https://doi.org/10.1021/j100820a009openalex-snapshot
QUANTUM EFFICIENCIES OF FLUORESCENCE OF ORGANIC SUBSTANCES: EFFECT OF SOLVENT AND CONCENTRATION OF THE FLUORESCENT SOLUTE1
inferredcites →https://doi.org/10.1021/ja00839a011openalex-snapshot
General definition of ring puckering coordinates
inferredcites →https://doi.org/10.1021/jo3016538openalex-snapshot
Bicarbazoles: Systematic Structure–Property Investigations on a Series of Conjugated Carbazole Dimers
inferredcites →https://doi.org/10.1039/9781788019491-00349openalex-snapshot
Phosphazenes
inferredcites →https://doi.org/10.1039/9781839163814-00429openalex-snapshot
Phosphazenes
inferredcites →https://doi.org/10.1039/b505236jopenalex-snapshot
Achiral molecules in non-centrosymmetric space groups
inferredcites →https://doi.org/10.1039/c3mh00079fopenalex-snapshot
A six-carbazole-decorated cyclophosphazene as a host with high triplet energy to realize efficient delayed-fluorescence OLEDs
inferredcites →https://doi.org/10.1039/c6nj02052fopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d0tc03866kopenalex-snapshot
Metal-free carbazole scaffold dyes as potential nonlinear optical phores: molecular engineering
inferredcites →https://doi.org/10.1039/d1nj00934fopenalex-snapshot
Phosphorus–nitrogen compounds. Part 54. syntheses of chiral amino-4-fluorobenzyl-spiro(N/O)cyclotriphosphazenes: structural and stereogenic properties
inferredcites →https://doi.org/10.1039/j19710001450openalex-snapshot
An improved determination of the crystal structure of hexachlorocyclotriphosphazene (phosphonitrilic chloride)
inferredcites →https://doi.org/10.1080/03086648508072743openalex-snapshot
AN ANSWER TO THE SPIRO VS ANSA DILEMMA IN CYCLOPHOSPHAZENES. PART VIII. THE FIRST FUSED DISPIROCYCLOTRIPHOSPHAZENES, N3P3CL2[HN[sbnd](CH2)m[sbnd]NH] [HN[sbnd](CH2)N[sbnd]NH](m ≠ n = 2,3,4)
inferredcites →https://doi.org/10.1080/07391102.2020.1846621openalex-snapshot
Synthesis and spectroscopic characterizations of hexakis[(1-(4′-oxyphenyl)-3-(substituted-phenyl)prop-2-en-1-one)]cyclotriphosphazenes: theirin vitrocytotoxic activity, theoretical analysis and molecular docking studies
inferredcites →https://doi.org/10.1080/10426507.2018.1469490openalex-snapshot
Syntheses and structural characterizations of 2-pyridyl(N/O)spirocyclotriphosphazene derivatives
inferredcites →https://doi.org/10.1080/10426507.2020.1723096openalex-snapshot
Synthesis, structural characterization and antimicrobial activities of cyclochlorotriphosphazene derivatives derived from N-(1-Naphthyl)ethylenediamine
inferredcites →https://doi.org/10.1080/14756366.2017.1419216openalex-snapshot
N-thioalkylcarbazoles derivatives as new anti-proliferative agents: synthesis, characterisation and molecular mechanism evaluation
inferredcites →https://doi.org/10.1107/s0021889812029111openalex-snapshot
WinGX and ORTEP for Windows : an update
inferredcites →https://doi.org/10.1107/s0108767307043930openalex-snapshot
A short history of SHELX
inferredcites →https://doi.org/10.1107/s2053229614024218openalex-snapshot
Crystal structure refinement with SHELXL
inferredcites →https://doi.org/10.1134/s1070363221120276openalex-snapshot
Vanillinato-Substituted Monospirocyclotriphosphazenes: Synthesis, Spectroscopic and Crystallographic Characterizations, and Thermal Properties
inferredcites →https://doi.org/10.2174/1385272824999201001154127openalex-snapshot
Cyclotriphosphazene-based Derivatives for Antibacterial Applications: An Update on Recent Advances
inferredcites →https://doi.org/10.3390/molecules26134017openalex-snapshot
AB5 Derivatives of Cyclotriphosphazene for the Synthesis of Dendrons and Their Applications
inferredcites →https://doi.org/10.3390/polym13172916openalex-snapshot
A Review on Synthesis, Structural, Flame Retardancy and Dielectric Properties of Hexasubstituted Cyclotriphosphazene
inferredcites →https://doi.org/10.3906/kim-1908-17openalex-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.4751194openalex-extracted
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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
inferred← citeshttps://doi.org/10.1007/s11164-023-04984-xopenalex-snapshot
Phosphorus-nitrogen compounds: Part 69—Unsymmetrical dispiro(N/N)cyclotriphosphazenes containing different pendant arms: syntheses, characterization, stereogenism, photophysical and bioactivity studies
inferred← citeshttps://doi.org/10.1007/s11164-024-05285-7openalex-snapshot
Phosphorus–nitrogen compounds: part 75—design, synthesis, stereogenic and conformational properties of chiral dispiro(N/N)cyclotriphosphazenes: structural analysis and photophysical and bioactivity studies
inferred← citeshttps://doi.org/10.1007/s11164-025-05603-7openalex-snapshot
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
inferred← citeshttps://doi.org/10.1007/s11696-025-04259-2openalex-snapshot
Bioactivity, free radical scavenging properties, hCA I and hCA II esterase activities of tetraamino-(9-ethyl-3-carbazolyl)-(NN)-spirocyclotriphosphazenes: Synthesis, characterization, and structure–activity relationship (SAR) studies
inferred← citeshttps://doi.org/10.1016/j.fbio.2024.104826openalex-snapshot
Cyclotriphosphazenes: Pre-harvest foliar applications improve antioxidant activity by increasing phenolic compounds in Lavandula angustifolia Mill.
inferred← citeshttps://doi.org/10.1016/j.ica.2024.121936openalex-snapshot
New cyclotriphosphazenes with butylated oxyanisole motif; synthesis, characterization and biological properties
inferred← citeshttps://doi.org/10.1016/j.ica.2024.121953openalex-snapshot
Synthesis of N,N-spiro-bridged bis(cyclotriphosphazene) derivatives bearing aryl thio groups and their comparison with alkoxy and amino derivatives
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.molstruc.2024.138305openalex-snapshot
Phosphorus-nitrogen compounds. Part 72. Bisspiro(N/N)cyclotri-phosphazenes with 4-chlorobenzyl and ferrocenyl pendant arms: Synthesis, structural characterization, dye-sensitized solar cell fabrication and antituberculosis activity studies
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139047openalex-snapshot
The first synthesis and characterization of spiro and ansa-cyclotriphosphazenes with 3-Hydroxyflavone and induction of apoptosis in breast cancer (MCF-7)
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.141926openalex-snapshot
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.2025.143614openalex-snapshot
Phosphorus-nitrogen compounds: Part 81. Syntheses and characterizations of the novel lithium complexes of monoferrocenylspirocyclotriphosphaza-crown ethers
inferred← citeshttps://doi.org/10.1016/j.pmatsci.2024.101232openalex-snapshot
Cyclotriphosphazene based materials: Structure, functionalization and applications
inferred← citeshttps://doi.org/10.1016/j.poly.2024.117252openalex-snapshot
Synthesis and characterization of novel spiro-(2,2′-dioxybiphenyl)-cyclotriphosphazene derivatives bearing butylated oxyanisole groups and their antioxidant and antimicrobial activities
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c02206openalex-snapshot
Phosphorus–Nitrogen Compounds: Part 76. Design and Syntheses of Dispiro- and Trispiro(N/N)cyclotriphosphazenes: Conformational and Structural Analyses, Chirality, Electrochemical, Dye-Sensitized Solar Cells, and Bioactivity Studies
inferred← citeshttps://doi.org/10.1039/d3nj01956jopenalex-snapshot
Designing inorganic–organic hybrid molecules based on carbazole/indole-appended cyclotriphosphazenes and the investigation of their photophysical properties
inferred← citeshttps://doi.org/10.1039/d3nj04099bopenalex-snapshot
Phosphorus–nitrogen compounds: part 71. Novel unsymmetrically-substituted dispiro-cyclotriphosphazenes: synthesis, characterization, antituberculosis activity, and phototunable charge storage studies
inferred← citeshttps://doi.org/10.1039/d5nj02457aopenalex-snapshot
Phosphorus–nitrogen compounds. Part 80. Design and synthesis of hybrid multiheterocyclic cyclotriphosphazene conjugates bearing unsymmetrical pendant arms: spectral and crystallographic characterization, bioactivity and structure–activity relationship (SAR) studies
inferred← citeshttps://doi.org/10.1080/10426507.2025.2456201openalex-snapshot
Phosphorus-nitrogen compounds. Part 77. The synthesis of novel ferrocenyl(N/O)spiro- and 2- cis -4-dichloro-ferrocenyl(N/O)ansa-cyclotetraphosphazenes with 9-ethyl-3-carbazolyl pendant arm(s): spectral, bioactivity, electrochemical and dye-sensitized solar cell fabrication studies
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