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1.
Homaid A. Al-Madfa Robert A. Shaw Sidit Ture 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-4):333-338
Abstract The reactions of hexachlorocyclotriphosphazatriene, N3 P3 CI6, with 2, 2-dimethylpropane-1, 3-diol yield monospiro-, N3 P3 Cl4 [(OCH2)2 CMe2, dispiro-, N3 P3 Cl4((OCH2)2CMe2|2, and trispiroderivatives, N3 P3 ((OCH2)2, CMe2]3. An ansa, N3 P3 CI4 [(OCH2)2 CMe2]2 and a spiro-ansa, N3 P3 Cl2- ((OCH2), CMe2,]2 and a doubly-bridged compound, (N3 P3 Cl4,)2[(OCH2)]2 were also isolated. Product types and relative yields were compared with those arising from propane-1, 3-diol. The yields of ansa products from the reactions of the dimethyl diol seem to be considerably enhanced relative to those of its unmethylated analogue. 31P and 1H n.m.r. spectra are reported. 相似文献
2.
Serap Beli Simon J. Coles David B. Davies Ayen O. Erkovan Michael B. Hursthouse Adem Kl 《Polyhedron》2009,28(16):3593-3599
Reaction of hexachlorocyclotriphosphazene, N3P3Cl6 (1), with the sodium derivative of the fluorinated diol, 2,2,3,3,4,4,5,5-octafluorohexane-1,6-diol, (2), in THF solution at room temperature afforded five products, whose structures have been characterised by 1H, 19F and 31P NMR spectroscopy: the mono-ansa compound N3P3Cl4[OCH2(CF2)4CH2O] (3); the single-bridged compound N3P3Cl5[OCH2(CF2)4CH2O]N3P3Cl5 (4), two double-bridged compounds N3P3Cl4(OCH2(CF2)4CH2O)2N3P3Cl4, (5-anti, 5-syn) and the triple-bridged compound N3P3Cl3(OCH2(CF2)4CH2O)3N3P3Cl3 (6). X-ray crystallographic studies confirmed the structures of the ansa compound (3), the double-bridged compound (5-anti) and the first example of a triple-bridged cyclotriphosphazene derivative (6). The results were also compared with those for reactions of (1) with analogous fluorinated shorter diols (1,4-butane- and 1,5-pentane-diols). It is found that on increasing the chain length of the diol, there is a decrease in the relative proportion of intramolecular reactions giving spiro and ansa derivatives and an increase in the amount of bridged cyclophosphazene derivatives via intermolecular reactions. 相似文献
3.
4.
Sedat Ture Rafig Gurbanov 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):620-629
AbstractThe reactions of hexachlorocyclotriphosphazene, N3P3Cl6 (1) with 1,1,3,3-tetramethyl-guanidine (2) in (1:1:2, 1:2:4 and 1:3:6) stoichiometries in THF and dichloromethane solutions under reflux yield a total of 4 novel products: three non-geminal derivatives, N3P3Cl4[NCN2(CH3)4]2 (3), N3P3Cl3[NCN2(CH3)4]3 (4) and N3P3Cl2[NCN2(CH3)4]4 (5); and one hexa-substituted product, N3P3[NCN2(CH3)4]6 (6). The structures of 3-6 have been determined mainly by elemental analysis, MS, 31P and 1H NMR spectral data. Furthermore, thermal characteristics of the synthesized compounds 4 and 6 were evaluated using Differential Scanning Calorimetric (DSC) measurements. NMR spectroscopic data, product types and relative yields are compared with those of the previously investigated derivatives of N3P3Cl6 (1) with mono and difunctional reagents. 相似文献
5.
Seung Seo Lee Pushpak Mizar Ozge Kucuk 《Phosphorus, sulfur, and silicon and the related elements》2020,195(6):454-463
AbstractThe reactions of cyclotriphosphazene (1) with 2-(2-hydroxyethylamino)-ethanol (2) were investigated. 2-(2-hydroxyethylamino)-ethanol (2) is a tri-functional reagent consisting of both aliphatic hydroxyl and the secondary amino groups and its nucleophilic substitution reactions with cylotriphosphazene can lead to different product types; open chain, spiro, ansa, bridged and their mixtures. The reactions with one, two and three equimolar ratios of 2-(2-hydroxyethylamino)-ethanol, in the presence of NaH at 0–10?°C and at room temperature gave the following cyclotriphosphazene derivatives: one mono-spiro, N3P3Cl4[O–(CH2)2–NH–(CH2)2–O] (3, 1:1, r.t.); its isomer mono-ansa (5, 1:1, r.t.); one dispiro, N3P3Cl2[O–(CH2)2–NH–(CH2)2–O]2 (4, 1:1, r.t.); its isomer spiro-ansa (6, 1:2, r.t.); and one single-bridged compound with spiro substituted units, N3P3Cl3[O–(CH2)2–NH–(CH2)2–O]3N3P3Cl3 (7, 1:3, at 0–10?°C); as well as single-, N3P3Cl5[O–(CH2)2–NH–(CH2)2–O]N3P3Cl5 (8, 1:2, r.t.), double-, N3P3Cl4[O–(CH2)2–NH–(CH2)2–O]2N3P3Cl4 (9, 1:2, r.t.), and tri-bridged, N3P3Cl3[O–(CH2)2–NH–(CH2)2–O]3N3P3Cl3 (10, 1:3, at 0–10?°C) derivatives. Triple-bridged derivative is the major product in this system. The structures of the novel-derived compounds were characterized by TLC-MS, FT-IR, elemental analysis, 1H, and 31P NMR spectral. 相似文献
6.
Sorab R. Contractor Michael B. Hursthouse Harold G. Parkes Leylacaron S. Shaw Robert A. Shaw Hamza Yilmaz 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-3):149-152
Abstract Mono-(N3P3Cl4Y2), bis-(N3P3Cl2Y4) and tris-spiro derivatives (N3P3Y6) have been prepared with ethylene, 1, 3-propylene and 1,4-butylene glycols (Y2 = glycol residue). The 1H NMR spectra of mono- and tris-derivatives are relatively simple; those of the bis- very complex due to the intrinsic asymmetry of the methylene protons. This effect is made use of in studying the replacement pattern of N3P3Cl4 [O (CH2)3O] with primary and secondary amines. Homonuclear 1H decoupling simplifies the spectra and allows an unambiguous distinction to be made between the different isomeric possibilities of the bis amino derivatives N3P3Cl2R2 [O(CH2)3O] where R = amino residue. Primary amines give geminal, secondary amines nongeminal trans-derivatives. The trans-structure of the bis-pyrrolidino derivative has been confirmed by X-ray crystallography. 相似文献
7.
The reaction of the octachlorocyclotetraphosphazene, N4P4Cl8 (1), in three stoichiometries (1:1, 1:2 and 1:3) with the sodium derivative of the fluorinated diol, 2,2,3,3-tetrafluorobutane-1,4-diol (2), in THF solution at room temperature produced seven products, whose structures have been characterized by elemental analysis, mass spectrometry, 1H, 19F, 31P NMR spectroscopy and by X-ray crystallography, where suitable single crystals were obtained: the mono-spiro compound, N4P4Cl6(OCH2CF2CF2CH2O) (3), its ansa isomer (4), cis- and trans-bis-spiro derivatives N4P4Cl4(OCH2CF2CF2CH2O)2 (5 and 6), tris-spiro compound N4P4Cl2(OCH2CF2CF2CH2O)3 (7), its mono-spiro-bis-ansa isomer (8) and tetrakis-spiro compound N4P4(OCH2CF2CF2CH2O)4, (9). X-ray crystallographic studies confirmed that the structure of the mono-spiro-bis-ansa isomer (8) has been reported as a first example in the literature. The results of all reactions were compared with previous work on the reaction of hexachlorocyclotriphosphazene, N3P3Cl6 with the sodium derivative of the diol (2), in a 1:1.2 mole ratio in the in the same solvent, THF, and with the reaction of octafluorocyclotetraphosphazene, N4P4F8, with the silyl derivative of the diol (2), (Me3SiOCH2CF2)2, in a 1:0.4 mole ratio in THF. 相似文献
8.
Sedat Ture 《Phosphorus, sulfur, and silicon and the related elements》2016,191(1):129-139
The reactions of octachlorocyclotetraphosphazatetraene, N4P4Cl8 (1) with difunctional aliphatic reagent, HO-(CH2)5-OH (3) have aroused a good deal of attention, and four types of products have been realized: one 2-open chain-(1′-oxy-5′-hidroxy-pentane)-2,4,4,6,6,8,8-heptachlorocylotetraphosphazatetraene, N4P4Cl7[O(CH2)5OH] (4); one 2,2-mono-spiro-(1′,5′-pentanedioxy)-4,4,6,6,8,8-hexachlorocyclotetraphosphazatetraene, N4P4Cl6[O(CH2)5O] (5); its isomers 2,4-mono-ansa-((1′,5′-pentanedioxy)-2,4,6,6,8,8- hexachlorocyclotetraphosphazatetraene (6) and 2,6-mono-ansa-(1′,5′-pentanedioxy)-2,4,6,6,8,8-hexachlorocyclotetraphosphazatetraene (7); one 2,2,6,6-dispiro-(1′,5′-pentanedioxy)-4,4,8,8-tetrachlorocyclo- tetraphosphazatetraene, N4P4Cl4[O(CH2)5O]2 (8); two isomeric 2,4,6,8-bisansa-(1′,5′-pentanedioxy)-2,4,6,8-tetrachlorocyclotetraphosphazatetraene (9) and 2,6,4,8-bisansa-(1′,5′-pentanedioxy)-2,4,6,8-tetrachloro-cyclotetraphosphazatetraene (10); one 4,4,8,8-dispiro-2,6-ansa- (1′,5′-pentanedioxy)-2,6-dichlorocyclotetra-phosphazatetraene, N4P4Cl2[O(CH2)5O]3 (11), one 2,2,4,4,6,6-trispiro-(1′,5′-pentanedioxy)-8,8-dichlorocyclo-tetraphosphazatetraene, N4P4Cl2[O(CH2)5O]3 (12); and a 2,2,4,4,6,6,8,8-tetraspiro-(1′,5′-pentanedioxy)-cyclotetraphosphazatetraene derivative, N4P4[O(CH2)5O]4, (13). The respective structures were deduced by means of elemental analysis, mass spectrum, and 31P, 1H, and 13C nuclear magnetic resonance spectroscopic investigations. 相似文献
9.
Gönül Yenilmez Çiftçi Hakan Dal Esra Tanrıverdi Eçik Tuncer Hökelek Adem Kılıç Elif Şenkuytu 《Polyhedron》2010
In this study, the crystal structures of the dispiroansa spermine derivatives of cyclotriphosphazene are characterised for the first time. The reaction of spiro-, gem-disubstituted cyclotriphosphazene derivatives, N3P3Cl4R2 [R = NHPh, (HN(CH2)3NH)0.5, (OCH2C(CH3)2CH2O)0.5], (1–3), with spermine (4), in aprotic solvents such as CH2Cl2 results in a series of dispirobino spermine derivatives of cyclotriphosphazene (5a, 6a, 7), namely spermine bridged compounds. Whereas, in protic solvents such as CHCl3 give, dispiroansa derivatives (8–10) namely tetracyclic cyclotriphosphazene. The new series of dispirobino and dispiroansa spermine derivatives of cyclotriphosphazene (5a, 6a, 7–10) have been characterised by elemental analysis, mass spectrometry, X-ray (for 5a, 8, 10) and 1H, 31P NMR spectroscopies. 相似文献
10.
AbstractReactions of non-gem-hexanedioxytetrachlorocyclotriphosphazene (1) with monofunctional nucleophilic reagents, 2-(2-hydroxyethyl)thiophene (2), benzyl alcohol (3) and 1,1,3,3-tetramethylguanidine (4) were investigated. The reactions, using an excess of NaH, in THF solutions, under refluxing conditions and with 1:2?mole ratios allow the synthesis of the following novel cyclotriphosphazene derivatives: 2,4-dichloro-2,4-(hexane-1,6-dioxy)-6,6-[2-(2-ethoxy)hiophene]-cyclotriphosphazatriene, N3P3Cl2[O(CH2)6O-(C6H8OS)2] (5); 2,4-(hexane-1,6-dioxy)-2,4,6,6-[2-(2-ethoxy) thiophene]-cyclotriphosphazatriene, N3P3[O(CH2)6O-(C6H8OS)4] (6); 2,4-dichloro-2,4-(hexane-1,6-dioxy)-6,6-(methoxybenzene)-cyclotriphosphazatriene, N3P3Cl2[O(CH2)6O-(C6H5CH2O)2] (7); 2,4-(hexane-1,6-dioxy)-2,4,6,6-(methoxybenzene)-cyclotriphosphazatriene, N3P3[O(CH2)6O-(C6H5CH2O)4] (8); and 2,4-dichloro-2,4-(hexane-1,6-dioxy)-6,6-(1,1,3,3-tetramethyguanidine)-cyclotriphosphazatriene, N3P3Cl2[O(CH2)6O-HN-CN2(CH3)4] (9). The structures of the synthesized compounds (5–9) have been characterized by elemental analysis, TLC-MS, 1H, 13C and 31P {+1H} and {?1H} NMR spectral data. 相似文献
11.
Treatment of [Ru(PPh3)3Cl2] with one equivalent of tridentate Schiff base 2-[(2-dimethylamino-ethylimino)-methyl]-phenol (HL) in the presence of triethylamine afforded a ruthenium(III) complex [RuCl3(κ2-N,N-NH2CH2CH2NMe2)(PPh3)] as a result of decomposition of HL. Interaction of HL and one equivalent of [RuHCl(CO)(PPh3)3], [Ru(CO)2Cl2] or [Ru(tht)4Cl2] (tht = tetrahydrothiophene) under different conditions led to isolation of the corresponding ruthenium(II) complexes [RuCl(κ3-N,N,O-L)(CO)(PPh3)] (2), [RuCl(κ3-N,N,O-L)(CO)2] (3), and a ruthenium(III) complex [RuCl2(κ3-N,N,O-L)(tht)] (4), respectively. Molecular structures of 1·CH2Cl2, 2·CH2Cl2, 3 and 4 have been determined by single-crystal X-ray diffraction. 相似文献
12.
S. N. Adamovich R. G. Mirskov A. N. Mirskova M. G. Voronkov 《Russian Journal of General Chemistry》2010,80(10):1972-1973
Reaction of tris(2-hydroxyethyl)amine hydrochloride Cl− N+H(CH2CH2OH)3 with zinc diacetate and bis(2-methylphenoxy)acetate in the molar ratio 2: 1 results in complexes 2[Cl− N+H(CH2CH2OH)3]· Zn (OCOR)2 (I, II) R= Me (I), 2-MeC6H4OCH2 (II), which contain two protatrane cations linked with zinc diacylate by two coordination bonds HO → Zn. Complexes I and II are also formed by the reaction of the corresponding tris(2-hydroxyethyl)amine hydrochloride acylate RCOO−N+H(CH2CH2OH)3 with ZnCl2. The structure of complexes I, II is proved by elemental analysis, IR and 1H, 13C, 15N NMR spectroscopy. 相似文献
13.
Sedat Ture 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):1156-1171
Abstract From the reactions of hexachlorocyclotriphosphazatriene, N3P3Cl6 (1) with pentane-1,5-diol (2) in dichloromethane solution, the following derivatives have been isolated: 2,2-spiro(1′,5′-pentanedioxy)-4,4,6,6-tetrachlorocyclotriphosphazatriene, N3P3Cl4[O(CH2)5O] (3); its ansa isomer, 1,3-ansa(1′,5′-pentanedioxy)-1,3,5,5-tetrachlorocyclotriphosphazatriene, (4); bis spiro(1′,5′-pentanedioxy)-6,6-dichlorocyclotriphosphazatriene, N3P3Cl2[O(CH2)5O]2 (5); its spiro-ansa isomer, (1′,5′-pentanedioxy)-1,3-dichlorocyclotriphosphazatriene (6); as well as the bino(1,5-pentanedioxy)-di-(pentachlorocyclotriphosphazatriene), N3P3Cl5 [O(CH2)5O]N3P3Cl5 (7), and tri-bino(1,5-pentanedioxy)-di (trichlorocyclotriphosphazatriene), N3P3Cl3[O(CH2)5O]3N3P3Cl3, (8) derivatives. Their structures were established by MS and NMR with the use of 1H, 13C, and 31P spectroscopy. Product types and relative yields are compared with those of the previously investigated diol derivatives. The yield of the mono-ansa product (25%) obtained in this system was considerably increased relative to those of the propane-1,3-diol derivative (11.2%) and decreased relative to the 2,2-dimethyl-propane-1,3-diol (36.2%), and bis(2-hydroxyethyl) ether (34.5%) derivatives. 相似文献
14.
The reaction of N-benzoylphosphoramidic dichloride with amines afforded some new N-benzoylphos-phoric triamides with formula C6H5C(O)NHP(O)(X)2, X=NH–CH(CH3)2 (1), NH–CH2–CH(CH3)2 (2), NH–CH2–CH(OCH3)2 (3), N(CH3)[CH2CH(OCH3)2] (4) and N(CH3)(C6H11) (5) that were characterized by 1H,13C,31P NMR, IR spectroscopy and elemental analysis. The structures have been determined for compounds 4 and 5 by X-ray crystallography. These compounds contain one amidic hydrogen atom and form centrosymmetric dimmers via intermolecular
–P–O⋯H–N–hydrogen bonds besides weak C–H⋯O hydrogen bonds that lead to three-dimensional polymeric clusters in the crystalline
lattice. 相似文献
15.
Solvatothermal syntheses have been exploited to effect the isolation of three novel polyoxoalkoxometalate clusters, [{Fe(OH)(CH3CN)2} Fe6OCl6{(OCH2)3CCH2OH}4] (1), [Fe10O2Cl8{(OCH2)3CCH2CH3}6] (2), and [(VO)2Fe8O2Cl6{(OCH2)3CCH2CH3}6] (3). The structure of 1 may be described as a hexametalate core {Fe6OCl6}10+, consisting of a octahedral arrangement of chloride ligands encasing an octahedron of six Fe(III) sites, with a central oxo group. The remaining four coordination sites at each octahedral iron center are occupied by doubly bridging oxygen donors from the trisalkoxo ligands. One triangular face of this substructure, defined by three oxygen atoms, from three adjacent trisalkoxo ligands, is capped by the {Fe(OH)(CH3CN)2}2+ subunit. The structure of 2 is based on the decametalate core of edge-sharing octahedra. The eight peripheral Fe(III) sites of the cluster bond to four oxygen donors from the trisalkoxo ligands, a terminal Cl– ligand, and one of the
6-oxo groups. The two central iron sites are linked to four oxygen donors from the trisalkoxo ligands and to both of the
6-oxo groups. Cluster 3 is structurally related to 2 with two {FeCl}2+ units replaced by {VO}2+ groups. 相似文献
16.
《Journal of Coordination Chemistry》2012,65(7):1180-1186
Ligand bridged homodinuclear derivatives of bismuth(V) of the type, (1a–1d) [where R =–C(CH3)2CH2CH(CH3)–(1a),–CH(CH2CH3)CH2–(1b),–CH(CH3)CH(CH3)–(1c),–CH(CH3)CH2–(1d)] have been synthesized by reactions of equimolar oxobis(triphenylbismuth)dichloride, {[Ph3Bi]2O}Cl2 with glycols, HOROH in the presence of NaOMe. Reactions of sodiumtetraisopropoxoarsonate, NaAs(OPri)4 with in 1 : 1 molar ratio yielded homodinuclear alkoxo derivatives of arsenic(III) containing glycols, (2a–2d). All compounds were characterized by elemental analysis, molecular weight determinations, IR and NMR (1H and 13C) spectral studies. 相似文献
17.
Thouraya Barhoumi-Slimi M. A. K. Sanhoury M. T. Ben Dhia M. R. Khaddar 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1827-1834
Abstract The synthesis of octahedral complexes [SnCl4L2] (L = R2NP(O)(OCH2CF3)(O-p-tolyl): R2N = Me2N (1), Et2N (2), CH2(CH2CH2)2N (3), and O(CH2CH2)2N (4), or L = R2NP(O)(OCH2CF3)(O-p-PhNO2): R2N = Me2N (5), Et2N (6), and O(CH2CH2)2N (7) is described. The new adducts have been characterized by multinuclear (31P, 19F, 119Sn) NMR, IR spectroscopy, and elemental analyses. The solution NMR data show the presence of a mixture of cis and trans isomers. The structure of the complexes in solution was further confirmed by 119Sn NMR spectra, which display a triplet for each isomer, indicating an octahedrally coordinated tin center. The effects of the nature of R and Ar substituents on the donor ability of the P=O group in the ligands R2NP(O)(OCH2CF3)(OAr) were investigated on the basis of 119Sn NMR chemical shifts and used to classify these ligands according to their Lewis basicity. 相似文献
18.
Arto Valkonen Katri Laihia Erkki Kolehmainen Reijo Kauppinen Pál Perjési 《Structural chemistry》2012,23(1):209-217
1H and 13C NMR chemical shifts have been determined and assigned based on PFG 1H, 13C HMQC, and HMBC experiments for 3-(4′-X-benzyl)-4-chromenones (Ia, X = CN and Ib, X = NO2), 3-(4′-X-benzyl)-4-thiochromenones (IIa, X = Cl and IIb, X = Br), (E)-3-(4′-X-benzylidene)-4-chromanones (IIIa–IIIe, X = OCH3, CH3, Cl, N(CH3)2, Br), (Z)-3-(4′-X-benzylidene)4-thiochromanones (IVa–IVd, X = Cl, Br, F, OCH3), 2-benzyl-1,2,3,4-tetrahydro-1-naphthol (V), 2-benzyl- and (E)-2-benzylidene-1-tetralones (VI and VII), and (E)-2-benzylidene-1-benzosuberol (VIII). The crystal structures have been determined for the following seven compounds: derivatives of 4-chromanones (IIIa–IIId), 1-tetrahydronaphtol (V), and 1-tetralones (VI and VII). The molecular features and intermolecular interactions in crystal state have been discussed. 相似文献
19.
Investigations on the Synthesis,Structural Characterization,and Crystal Structures of Three Diiron and Tetrairon Azadithiolate Complexes
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Li‐Ke Zou Cheng‐Long Deng Yao Li Jiao He Jian Wei Yu Wu Bin Xie Pei‐Hua Zhao Yu‐Long Li 《无机化学与普通化学杂志》2017,643(9):601-606
Three diiron and tetrairon azadithiolate complexes as models for the active site of [FeFe] hydrogenase were prepared. Reaction of complex Fe2(SCH2OH)2(CO)6 and NH2CH2CH2CH2OCH3 resulted in the diiron azadithiolate hexcarbonyl complex Fe2[(SCH2)2NCH2CH2CH2OCH3](CO)6 ( 1 ) in moderate yield. Furthermore, treatment of complex 1 with mono phosphine ligand PPh3 and diphosphine ligand Ph2PCH2CH2PPh2 in the presence of decarbonylation reagent Me3NO · 2H2O yielded the phosphine‐substituted azadithiolate complexes Fe2[(SCH2)2NCH2CH2CH2OCH3]CO)5(PPh3) ( 2 ) and {Fe2[(SCH2)2NCH2CH2CH2OCH3](CO)5}2(Ph2PCH2CH2PPh2) ( 3 ) respectively. The new complexes 1 – 3 were fully characterized by elemental analysis, IR, 1H, 13C, 31P NMR spectroscopy and X‐ray crystallography. It is worthy to note that the crystallographic studies show the unusual difference of the methoxypropanyl substituent on the N atom of complexes 1 and 2 , largely because of the affection of phosphine ligand PPh3. In addition, complex 1 was found to be a catalyst for H2 production under electrochemical condition. 相似文献
20.
Sedat Ture 《Phosphorus, sulfur, and silicon and the related elements》2016,191(8):1174-1182
Reactions of hexachlorocyclotriphosphazene N3P3Cl6 (1) with 1,4-butane-(2) and 1,6-hexane-diols (3) in (1:1:2, 1:2:4, and 1:3:6) stoichiometries in THF solution at room temperature (r.t.) and under refluxing conditions yield a total of 15 products: two open chain, N3P3Cl5[O(CH2)nOH] (n = 4, 6) (4, 5), two mono-spiro, N3P3Cl4[O(CH2)nO] (n = 4, 6) (6, 7), two mono-ansa, N3P3Cl4[O(CH2)nO] (n = 4,6) (8, 9), two dispiro, N3P3Cl2[O(CH2)nO]2 (n = 4, 6) (10, 11), two spiro-ansa, N3P3Cl2[O(CH2)nO]2 (n = 4, 6) (12, 13), one tri-spiro, N3P3[O(CH2)4O]3 (14), two single-bridged, N3P3Cl5[O(CH2)nO]N3P3Cl5 (n = 4, 6) (15, 16), one double-bridged, N3P3Cl4[O(CH2)6O]2N3P3Cl4 (17), and one tri-bridged, N3P3Cl3[O(CH2)6O]3N3P3Cl3 (18) derivatives. Their structures have been elucidated by MS, 31P, and 1H NMR spectroscopy. The results obtained, based on the synthesis, characterization, product types, and the relative yields, are compared with those of previous studies on the reactions of 1 with 1,2-ethane-, 1,3-propane-, 1,4-butane-, 1,5-pentane-, and 1,6-hexane-diols. 相似文献