Glasses of a chemical composition 400CeO₂∙60P₂O₅ have been prepared using ordinary slowly cooling technique. Reagent grades (Aldrich company) CeO₂ and NH₄H₂PO₄ (purity 98.93, 99.89) are the raw materials used in glass preparation. The glasses were prepared by melting the mixtures in an aluminum crucible in an electric furnace at about 1250˚C. After solidification of the glass, it reheated in an electric furnace at tempering temperature of 300˚C for 3 hours to release internal stresses.

XRD diffraction measurements were carried out on a Brucker Axs-D8 spectrometer. Emitting source of type (λCuKα) has been utilized. The numerical data were frequently accumulated with a small scanning step, 2θ rang of 5˚ - 70˚ and a dwell time of 0.4 seconds have been applied. The obtained X-ray diffraction spectra were revised to reference samples related to standards which were gathered by the technique of powder diffraction and standards (JCDPS). The surface structure of the investigated samples was characterized using JEOL JSM-6510 LV electron microscope operated at accelerating voltage 30 KV, with a magnification 10× up to 400.000×. For the SEM study, the samples were coated with gold to prevent scattering of the electron beam. The FTIR absorption spectra were recorded using the KBr pellet technique. A Mattson 5000 FTIR spectrometer, with a 2 cm⁻¹ resolution, was used to obtain the spectra in the range 400 - 4000 cm⁻¹ at room temperature. In average 20 scans are accumulated to form the spectrum of each sample. ³¹P NMR spectra of powdered samples were recorded with a spectrometer operating at 11.74T (Joel -500, Mansoura University). Pulses with 10 s delay time were used and about 500 scans are obtained.

Phosphate GICs containing metal-Phthalocyanines (M-PCs) have been previously studied in terms of changing M-PCs concentrations [14] [18] [19] [20] . In the present research, we enlarge the range of study by fixing the doping level and change the dopant type. The structure and some properties of three different types of metallic (Ga, Co, Fe) Phthalocyanines have been studied in the present work.

Figure 1 reflects the effect of changing the doping type on the visual or appearance of GICs. As presented in Figure 1, cerium phosphate glass of P/Ce molar ratio = 1.5 (Figure 1(a)) has the yellowish color. GICs of 0.8 Ga, Co and Fe-Phthalocyanines have a dark blue, dark violet and black color, Figures 1(b)-(d), respectively. The change of the color is considered due not only to changing the valence state of the metallic cation but also due to changing its coordination number in the corresponding matrix of GIC [14] .

As shown from Figures 1(a)-(d) there is a clear difference among the color of GICs containing different types of transition metal complexes. The change of color in the investigated GIC may be raised from electronic transitions between levels whose spacing corresponds to the wavelengths available in the visible light [1] [17] . These transitions are frequently referred to as d-d transitions because they involve the orbitals that are mainly d in character. Specifically, the exhibited colors are intimately related to the magnitude of the spacing between the energy levels which depend on the geometry of the complex, the nature of the ligands,

and the oxidation state of the central metal atom. In some cases the origin of the color is not only due to the d-d transitions, but also it may be due to charge transfer between central atom and the ligand (such as molecules which coordinated to central atoms, O, PO₄ groups and etc.). Similar to d-d transitions, charge-transfer (CT) transitions also involve the metal d-orbitals. Legend to metal charge transfer from O²⁻ to Ga, Co ((VII), Ce, Fe), described as LMCT band is simply accessible to occur in the investigated materials. In this case the charge transfer occurs from Fe(II) to the empty π* orbital of legend. Then charge transfers absorptions can be also considered due to movement of electrons between metal and ligand. This process is often 1000 times stronger than d- d transition bands [1] [14] [16] [17] .

As can be observed in Figure 2, it is interesting to compare the peak position (chemical shift values) of the NMR spectra of the investigated materials containing Ga, Co, and Fe Phthalocyanine (spectral c, d, and e) with that of metal free sample (a, b). As would be expected, the full width at half maximum (FWHM) and the spectral area of M-PC free samples (a, base glass, b base GIC) is much higher than that of samples containing M-PC (c, d and e).

The spectra of the free metal glass contain two resonance peaks at different values of chemical shifts (−27.5 and −33 ppm). On the other hand, spectra of samples containing Ga, Co and Fe-PCs have shown symmetric spectra with one specific value of chemical shift (−33 ppm) for Ga and Co and −35 ppm for Fe-PC. This may reflect the change of the bond character on the phosphors central

atoms [19] [20] [21] . These differences are attributed to the presence of the more electronegative metal ions bonded through the NBO in the PO₄ units. From the feature of the spectra (a and b), the ³¹PNMR studies suggest an increase in the magnitude of non-bridged oxygen atoms (NBO) around the phosphate atoms. But in samples containing M-PSC (c, d, e), there is an increasing of the group types bonded to NBO atoms in the phosphorus. This consideration is based on the large change between NMR spectra of a metal free and the metal containing samples which are evidenced from Figure 2. As can be seen from spectra (c, d, e), one symmetric resonance peak at the same value of chemical shift (−33 ppm) is only recorded for samples containing Ga and Co-PCs and lower value of −35 ppm is recorded for Fe-PC. On comparison to M-PSc free materials, spectra of duple resonance are presented (a, b).

Generally, NMR spectra of the as prepared 40CeO₂-60P₂O₅ glass have showed two broad peaks around −27.5 and −33 ppm assigned to mixtures from both meta and pyrophosphate environments. The ³¹P MAS-NMR spectra of the Ga, Co and Fe Phthalocyanine (c, d, e) show a similar pattern of lines. A chemical shift values found around −33 ppm for Ga and Co, (c, d) and at −35 ppm for Fe-PSC (e) are the features of the obtained spectra.

The broad peak at −27.5 ppm in the original glasses is decreased and resonance peak at −33 ppm is resolved via addition of 0.8 mol% metal Phthalocyanine. These changes lead to suggest that, addition of a fixed value of metallic (Ga, Co, Fe) Phthalocyanine affects significantly the phosphor environment in the glass structure. This suggests an additional mechanism that promotes the cross-linking reaction and therefore the setting of the cements. Generally, disappearing of resonance at −27.5 ppm and resolving of the resonance peak at −35 ppm as a result of addition of 0.8 metal Phthalocyanineis mainly due the forming of different bridging ligands in the second coordination spheres of P atoms [14] . Bridging of metals ligands with PO₄ groups should result in an increase in the number of bridging bonds between the central metal and PO₄ units which decrease the chemical shift of P muclei due to forming of the more shielded species. Specifically, the cements based on M-Phthalocyanine show different tendencies from that of free M-Phthalocyanine glasses. The negative chemical shifts are larger compared to the cement based on the metal. In addition, the peak intensity is increased and shifted toward more negative direction (spectra d). The change of the chemical shift is considered not only due to changing of the valence state of the metallic cation but also due to change of coordination number of phosphors atoms in the corresponding matrix of GIC.

X-ray diffraction spectra of the as prepared glass sample are presented by Figure 3(a). As can be seen from this figure, a broad band in the range of 25˚ - 40˚ of diffraction angles has been simply appeared. The broadening of this band can confirm the disordered structure of the base glassy material. Figure 3(b)

represents the spectra of the well prepared GIC containing 0.8 Ga. Three intense diffraction peaks which have been appeared at about 23˚, 28˚ and 38˚ are the main peak in the spectra. Structural analysis concerning the position of the both diffracted line spectra confirms a formation of metallic-phthalocyanine crystalline species of monoclinic structure [14] [22] [23] [24] . The Diffraction spectra presented by (c) (d) represent GICs of 0.8 mol%, Co and Fe-Phthalocyanine respectively. There are some sharp diffraction lines superimposed on the less broad diffraction patterns (c and d) in the GIC of 0.8 mol% Ga and Co and Fe-PSC. These spectra may represent two components of the well-formed structural configurations. One is due to the amorphous matrix (spectra a) and the other represent a crystalline matrix of the resined Ga and Co-PC (of spectra b and c). As a consequence, the spectra of glass of 0.8 mol% Ga and Co-PC contain a broad hump with a clear sharp diffraction peak. Much sharper diffraction peaks appear in sample of Fe-PSC (Figure 3(d)). In this case, the wide diffraction hump totally disappears confirming the presence of the highest crystalline phases, particularly in Fe-PSC GIC.

Figure 4 represents infrared spectra of oxide glass (a) and its GIC (b). It can be shown from Figure 4 and Figure 5 that there is an intensive absorbance at about 1800 cm⁻¹ represents the acid-base reaction, since this peak may represent C-O vibration in PO₄ groups [14] [20] . This intense peak didn’t appear in the spectra of the oxide glass, Figure 4(a). These changes may be considered due to the base-acid reaction which leads to degradation processes in material network [14] [20] .

Increasing crystallization (as presented by XRD, Figure 3) is also evidenced from IR spectra of GIC containing distinguished types from metal-Phthalocyanine Figure 5. The one resolved peak at about 750 cm⁻¹ in the spectra of both the glass and the GIC (a, b) is transformed to envelop of splitting absorbance peaks

around around 750 cm⁻¹ and 1800 cm⁻¹ in glasses containing Ga, Co, and Fe (figure c, d, e). X-ray diffraction and IR- absorbance spectra of GIC containing Fe is shown to contain much sharper peaks which lead to higher crystallinity.

The absorbance at about 590 cm⁻¹ can be related to the vibration of metallic ions Ga or Ce, (Co or Fe) in crystalline phosphate species [14] [16] [20] .

The GIC could simply be prepared by the method of acid-base reaction [14] [16] [17] [18] [19] [20] . Presence of metal-Phthalocyanine (PCs) as an essential counterpart of the present investigated GIC is necessary to control the synthesis and achieve their application [14] since they can play a role of chelating or complexing additive.

The investigated morphology of the base glass is shown in Figure 6. It can observe that an extremely homogenous glass network is the dominant. On the other hand, formulating the glass powder with the acid successfully results in forming some types of structural species called pitted glass particles [14] . The latter has been embedded in a polysalt main glass matrix (Figure 7). But formulation

of GIC with Co-Phthalocyanine has formed a morphology containing bundles like species (Figure 8). The latter type is changed to more thinner, elongated and aligned rod-like species (Figure 9). The well-formed fibers are characterized with very lower thickness and much higher length, as shown in Figure 9. The well-formed nano fibers with more enhanced shapes may be recommended as important materials which have specific applications in tissue engineering

or bio scaffolds. This may because the good affinity of carboxylate or peptide moieties for cerium phosphates pecies enhances the structure to simultaneously incorporate the precursor phosphate moieties which is called (grafting, Figure 9) throughout the self-assembled nano fibrous. The latter can be used as templates hybrid biomaterials [25] [26] [27] [28] .

Finally, we recommend that the acid-base reaction applied to get GIC has to be performed under relatively specific circumstances (pH around 4 - 4.5) which may help in minimizing the strict characteristics of phosphates of reduced pH values (<1.5). Such cases are considered to have importance to offer an elongated CePO₄ fiber which can be reflected from SEM micrograp (Figure 9).