A Surface Morphological Study, Poly(Vinyl Chloride) Photo-Stabilizers Utilizing Ibuprofen Tin Complexes against Ultraviolet Radiation

In this work, three Ibuprofen tin complexes were synthesized and characterized by Fourier Transform Infrared spectroscopy (FTIR), 1H and 119Sn-Nuclear Magnetic Resonance (NMR), and Energy Dispersive X-ray (EDX) spectroscopies to identify the structures. The complexes were mixed separately with poly(vinyl chloride) (PVC) to improve its photo-stability properties. Their activity was demonstrated by several approaches of the FTIR to exhibit the formation of new groups within the polymer structure due to the exposure to UV light. Moreover, the polymer’s weight loss during irradiation and the average molecular weight estimation using its viscosity before and after irradiation were investigated. Furthermore, different techniques were used to study the surface morphology of the PVC before and after irradiation. Field-emission scanning electron microscopy (FESEM) and optical microscope demonstrated that applying Ibuprofen tin complexes keeps the surface of PVC smoother, with fewer cracks and spots after irradiation comparing to the blank PVC. Finally, It seems possible that such synthesized Ibuprofen tin complexes can work as excellent photo-stabilizers of PVC. In particular, complex 1 showed the best results among other stabilizers due to the large conjugation system of the stabilizer.


Introduction
Many known tin (IV) complexes are related to the common prescription R x Sn(L) 4−x , where L could be an inorganic or organic ligand, and R is an aryl or alkyl group [1]. This type of complex comprises a tin center link to the anion, typically chloride, fluoride, hydroxide, oxide, thiolate, and carboxylate [2]. In the last five decades, thousands, or maybe millions, of organometallic compounds have been synthesized, where the greater number was for organotin materials. Hence, their applications in the industry as corrosion inhibitors, plastic photo-stabilizers, medical helpers, etc., have increased [3,4]. The main application of the organotin derivatives (about 70%) is as heat and light stabilizers in PVC pipes. In 1930, Germany and the United States manufactured PVC that consists of chlorinated hydrocarbon polymer. This polymer has been utilized widely around the world as one of the most important plastics because of its low cost, flame retardancy, chemical resistance, elasticity, light weight,

Synthesis of Bu 2 SnL 2 Complex (2)
A suitable amount of Ibuprofen (0.412 g; 2.0 mmol) was mixed with (0.303 g; 1.0 mmol) of dibutyltin chloride and left to stir for 8 h in boiling methanol (MeOH; 30 mL). After that, the mixture was cooled down to ambient temperature and filtered to give the crude product, which was washed with methanol to obtain the desired compound (complex 2).

Synthesis of Bu 2 SnOHL Complex (3)
A suitable amount of Ibuprofen (0.206 g; 1.0 mmol) was mixed with (0.248 g; 1.0 mmol) of dibutyltin oxide and left to stir for 6 h in boiling methanol (MeOH; 30 mL). Later, the mixture was cooled down to room temperature and filtered to give the crude product, which was washed with methanol to produce complex 3.

Preparation of PVC Films
PVC (5.0 g) in tetrahydrofuran (THF; 100 mL) was stirred at room temperature for two hours with 0.5 wt. % of the complexes to get a homogenous mixture. After that, it was poured into the glass plates to form homogenous films with a thickness of 40 µm. All prepared films were dried using a vacuum to remove the trace amount of solvent that could affect the measurements.

Utilizing the FTIR Technique to Investigate the Photo-Degradation of PVC
FTIR technique was also used to examine the photo-degradation of polymer films through following the formation and growth of carbonyl C=O and alkene C=C groups [29,30]. The functional group index (I s ) for both groups C=O and C=C was determined using the flowing equation [31].
where A s is the functional group absorbance and A r is the standard peak absorbance.

Utilizing the Weight Loss Technique to Investigate the Photo-Degradation of PVC
The photo-stability of PVC was also examined by calculating the weight loss of the polymer during irradiation time in the existence of the stabilizers. Hence, weight loss was calculated according to Equation (2).

Calculation of the Average Molecular Weight (M V ) of PVC
The intrinsic viscosity [η] of the polymer solution was measured, and the M V . of PVC after irradiation was measured according to Equation (3). This equation is called the Mark-Houwink equation [33].

Characterization of Synthesized Complexes
Three organotin(IV) complexes Bu 2 SnL 2 , Ph 3 SnL, and Bu 2 SnOHL were prepared by reacting di-and tri-organotin chlorides and di-organotin oxide with Ibuprofen as a ligand (L) under reflux conditions for 6-8 h in the presence of methanol as solvent (Schemes 1-3). Elemental analysis was used to clarify the elemental composition of the three prepared complexes and check the purity of them.
The high purity of Ibuprofen tin complexes made the complexes more stable. All data are presented in Table 1. The FTIR spectrum for Ibuprofen was compared with the spectra of organotin(IV) complexes to clarify the bonding sites of ligand molecules when coordinated with organotin(IV) compounds. All FTIR data of the prepared complexes and free ligands were summarized in Table 2. The presence of a broad peak in the FTIR spectrum of the ligand (Ibuprofen) at the region between 3000 and 3300 cm −1 was demonstrated. This peak is related to the stretching of the O-H bond of the carboxylic group. Thus, the peak disappeared in the ligand-tin complexes FTIR spectrum; this is clear evidence that the complexation has successfully happened after the deprotonation of the carboxylic group. The peak of carbonyl group ν(C=O) appeared at 1720 cm −1 and was shifted in the complexes toward lower frequency. The diagnostic bands for the carboxylate anti-symmetric [νas(COO)] are observed at 1627-1716, while the symmetric [ν(COO)] are observed at 1404-1423 cm −1 for stretching vibrations of complexes due to the complex formation. Calculating the change between νasy (COO) and νsy (COO) (ν) evaluates the possible mode of coordination of carboxylates to tin metal. The Δν (COO) values were obtained by the following equation [Δν (COO) = νasym (COO) − νsym (COO)] and the result showed that Δν (COO) is > 200 cm −1 . In this case, the Ibuprofen is considered as an asymmetric bidentate ligand [34].
Furthermore, the presence of peaks was demonstrated between 443 and 482 cm −1 , and 543 and 555 cm −1 , which are related to stretching Sn-O bond frequency, and stretching Sn-C bond frequency, respectively. This is obvious evidence regarding the complex formation [35].  The FTIR spectrum for Ibuprofen was compared with the spectra of organotin(IV) complexes to clarify the bonding sites of ligand molecules when coordinated with organotin(IV) compounds. All FTIR data of the prepared complexes and free ligands were summarized in Table 2. The presence of a broad peak in the FTIR spectrum of the ligand (Ibuprofen) at the region between 3000 and 3300 cm −1 was demonstrated. This peak is related to the stretching of the O-H bond of the carboxylic group. Thus, the peak disappeared in the ligand-tin complexes FTIR spectrum; this is clear evidence that the complexation has successfully happened after the deprotonation of the carboxylic group. The peak of carbonyl group ν(C=O) appeared at 1720 cm −1 and was shifted in the complexes toward lower frequency. The diagnostic bands for the carboxylate anti In this case, the Ibuprofen is considered as an asymmetric bidentate ligand [34].
Furthermore, the presence of peaks was demonstrated between 443 and 482 cm −1 , and 543 and 555 cm −1 , which are related to stretching Sn-O bond frequency, and stretching Sn-C bond frequency, respectively. This is obvious evidence regarding the complex formation [35].  The FTIR spectrum for Ibuprofen was compared with the spectra of organotin(IV) complexes to clarify the bonding sites of ligand molecules when coordinated with organotin(IV) compounds. All FTIR data of the prepared complexes and free ligands were summarized in Table 2. The presence of a broad peak in the FTIR spectrum of the ligand (Ibuprofen) at the region between 3000 and 3300 cm −1 was demonstrated. This peak is related to the stretching of the O-H bond of the carboxylic group. Thus, the peak disappeared in the ligand-tin complexes FTIR spectrum; this is clear evidence that the complexation has successfully happened after the deprotonation of the carboxylic group. The peak of carbonyl group ν(C=O) appeared at 1720 cm −1 and was shifted in the complexes toward lower frequency. The diagnostic bands for the carboxylate anti In this case, the Ibuprofen is considered as an asymmetric bidentate ligand [34].
Furthermore, the presence of peaks was demonstrated between 443 and 482 cm −1 , and 543 and 555 cm −1 , which are related to stretching Sn-O bond frequency, and stretching Sn-C bond frequency, respectively. This is obvious evidence regarding the complex formation [35].  The FTIR spectrum for Ibuprofen was compared with the spectra of organotin(IV) complexes to clarify the bonding sites of ligand molecules when coordinated with organotin(IV) compounds. All FTIR data of the prepared complexes and free ligands were summarized in Table 2. The presence of a broad peak in the FTIR spectrum of the ligand (Ibuprofen) at the region between 3000 and 3300 cm −1 was demonstrated. This peak is related to the stretching of the O-H bond of the carboxylic group. Thus, the peak disappeared in the ligand-tin complexes FTIR spectrum; this is clear evidence that the complexation has successfully happened after the deprotonation of the carboxylic group. The peak of carbonyl group ν(C=O) appeared at 1720 cm −1 and was shifted in the complexes toward lower frequency. The diagnostic bands for the carboxylate anti-symmetric [ν as (COO)] are observed at 1627-1716, while the symmetric [ν(COO)] are observed at 1404-1423 cm −1 for stretching vibrations of complexes due to the complex formation. Calculating the change between ν asy (COO) and ν sy (COO) (ν) evaluates the possible mode of coordination of carboxylates to tin metal. The ∆ν (COO) values were obtained by the following equation [∆ν (COO) = ν asym (COO) − ν sym (COO)] and the result showed that ∆ν (COO) is > 200 cm −1 . In this case, the Ibuprofen is considered as an asymmetric bidentate ligand [34]. Furthermore, the presence of peaks was demonstrated between 443 and 482 cm −1 , and 543 and 555 cm −1 , which are related to stretching Sn-O bond frequency, and stretching Sn-C bond frequency, respectively. This is obvious evidence regarding the complex formation [35].
The ligand and organotin(IV) complexes were also characterized by 1 H-and 119 Sn-nuclear magnetic resonance (NMR) in DMSO-d. The main signals of the chemical shift are listed in Table 3. 1 H NMR spectra showed all needed peaks to demonstrate the chemical structure of the ligand and complexes (1, 2, 3). As can be seen from Table 3, the chemical shifts of ligands shifted up and down filed when linked to Sn metal. These alternations in 1 H NMR chemical shift between the complexes and ligand are due to the different environments around the protons. A single peak in the 1 H-NMR spectrum at 12.27 ppm of the ligand is observed, which is related to the proton of the carboxylic group. Hence, this peak disappeared in the 1 H-NMR spectra of the complex due to the deprotonation of the carboxylic group after the complexation occurred. This indicates the bonding and coordination between ligand and complexes. The signal at 3.6 ppm corresponds to the HDO proton [36]. The 119 Sn-NMR spectra were verified in the DMSO-d 6 solvent for the three complexes. Di-organotin(IV) complexes give a resonance at −255.2 and −226.2 ppm, which are attributed to the 2 and 3 complexes, respectively. This fits within the range of six coordinated complexes. In the case of complex 1, the resonance of the 119 Sn was at −171.4 ppm, which indicates the Penta-coordinate of the complex [37]. The 119 Sn NMR, 1 H NMR, and FTIR spectra for the Ibuprofen and complexes were illustrated in the Supplementary Materials.

Utilizing FTIR Technique to Examine the Photo-Stability of PVC Films
The efficiency of the organotin(IV) complexes as light stabilizer of PVC was examined using the FTIR technique. The Irradiated PVC films with ultraviolet light at a maximum wavelength of 365 nm for 300 h caused an alteration in the FTIR spectrum. Three absorption peaks appeared in the infrared spectra of the PVC films after exposure to UV light. This could be attributed to the formation of hydroxyl 3500 cm −1 (OH), carbonyl 1722 cm −1 (C=O), and polyene 1604 cm −1 (C=C) groups [38]. As shown in Figure 1, a growth of three signals can be detected in the blank PVC after exposure to UV light for a long time, while the polymer with additives showed higher stability, and complex 1 was the most effective stabilizer. These three peaks are hydroxyl (OH) at 3500 cm −1 , carbonyl (C=O) at 1722 cm −1 , and polyene (C=C) at 1604 cm −1 groups. The growth rate of these peaks is related to the reference peak (1328 cm −1 ), which can be considered as a measure of the photo-degradation of PVC according to Equation (1) to determine I C=O and I C=C indices. They are plotted against irradiation time for the blank PCV and PVC + complexes using an interval time of 50-300 h of irradiation in Figures 2  and 3, respectively. Thereby, it has been demonstrated that both indices exhibit a significant reduction for I C=O and I C=C in the existence of additives with PVC compared to blank PVC. For instance, the I C=O values after 300 h of exposure to UV light were 0.599, 0.542, 0.413, and 0.287 for the PVC, PVC + 3, PVC + 2, and PVC + 1, respectively. Thus, with common qualities, the I C=C values decreased in the presence of additives as follows: 0.394, 0.334, 0.298, and 0.231 for PVC, PVC + 3, PVC + 2, and PVC + 1, respectively, after irradiation (300 h). Here, it can be concluded that all three stabilizers work to protect the PVC from photo-degradation and the best one is complex 1. This could be explained as complex 1 is linked to Ibuprofen and three phenyl groups that absorb within the UV region because of their conjugation system. Surfaces 2020, 3 FOR PEER REVIEW 6 complex 1 was the most effective stabilizer. These three peaks are hydroxyl (OH) at 3500 cm −1 , carbonyl (C=O) at 1722 cm −1 , and polyene (C=C) at 1604 cm −1 groups. The growth rate of these peaks is related to the reference peak (1328 cm −1 ), which can be considered as a measure of the photo-degradation of PVC according to Equation (1) to determine IC=O and IC=C indices. They are plotted against irradiation time for the blank PCV and PVC + complexes using an interval time of 50-300 h of irradiation in Figures 2 and 3 Here, it can be concluded that all three stabilizers work to protect the PVC from photo-degradation and the best one is complex 1. This could be explained as complex 1 is linked to Ibuprofen and three phenyl groups that absorb within the UV region because of their conjugation system.

Utilizing Weight Loss to Examine the Photo-Stability of PVC Films
Photo-degradation of PVC leads to dehydro-chlorination, and small organic residue elimination resulting in weight loss [39]. The weight loss of PVC was measured at 50 h intervals of irradiation using Equation (2). Figure 4 illustrates the alterations to the percentage of PVC weight loss at different irradiation times up to 300 h. Clearly, the PVC films containing complexes of organotin display a lower weight loss relative to that obtained for blank PVC.
Weight loss investigation is in agreement with the functional group indices effect since it shows that complex 1 demonstrated the best photo-stability against PVC photo-degradation. As mentioned above, this is due to the large aromatic conjugation system which is available in complex 1.

Utilizing Weight Loss to Examine the Photo-Stability of PVC Films
Photo-degradation of PVC leads to dehydro-chlorination, and small organic residue elimination resulting in weight loss [39]. The weight loss of PVC was measured at 50 h intervals of irradiation using Equation (2). Figure 4 illustrates the alterations to the percentage of PVC weight loss at different irradiation times up to 300 h. Clearly, the PVC films containing complexes of organotin display a lower weight loss relative to that obtained for blank PVC.
Weight loss investigation is in agreement with the functional group indices effect since it shows that complex 1 demonstrated the best photo-stability against PVC photo-degradation. As mentioned above, this is due to the large aromatic conjugation system which is available in complex 1.

Utilizing Weight Loss to Examine the Photo-Stability of PVC Films
Photo-degradation of PVC leads to dehydro-chlorination, and small organic residue elimination resulting in weight loss [39]. The weight loss of PVC was measured at 50 h intervals of irradiation using Equation (2). Figure 4 illustrates the alterations to the percentage of PVC weight loss at different irradiation times up to 300 h. Clearly, the PVC films containing complexes of organotin display a lower weight loss relative to that obtained for blank PVC.
Weight loss investigation is in agreement with the functional group indices effect since it shows that complex 1 demonstrated the best photo-stability against PVC photo-degradation. As mentioned above, this is due to the large aromatic conjugation system which is available in complex 1.

Calculation of the Average Molecular Weight ( ) by Utilizing Viscosity
An estimate the average molecular weight of the polymer was obtained using viscosity. Hence, the degradation causes the breaking of the polymer chain, which leads to decreasing the polymer's molecular weight [40]. The PVC solution viscosity is used to measure the . The irradiated PVC films were dissolved in the THF and the viscosity was measured using a viscometer [33]. The for each film at different irradiation times was calculated using Equation (3). Figure 5 shows the against irradiation time for the blank and additive-filled PVC. The of PVC film was reduced dramatically during the irradiation process. As a result, the for blank PVC film was approximately 170,100 at the beginning and decreased to 12,700 after 300 h of irradiation, while the of PVC + 3, PVC + 2, and PVC + 1 were 26,200, 35,400, and 44,600 at same conditions. Obviously, this study is in good agreement with the functional groups and weight loss studies. PVC + 1 has the highest among other stabilizers, which means Ph3SnL (1) is the best photo-stabilizer of PVC against photo-degradation.

Calculation of the Average Molecular Weight (M V ) by Utilizing Viscosity
An estimate the average molecular weight of the polymer was obtained using viscosity. Hence, the degradation causes the breaking of the polymer chain, which leads to decreasing the polymer's molecular weight [40]. The PVC solution viscosity is used to measure the M V . The irradiated PVC films were dissolved in the THF and the viscosity was measured using a viscometer [33]. The M V . for each film at different irradiation times was calculated using Equation (3). Figure 5 shows the M V . against irradiation time for the blank and additive-filled PVC. The M V of PVC film was reduced dramatically during the irradiation process. As a result, the M V for blank PVC film was approximately 170,100 at the beginning and decreased to 12,700 after 300 h of irradiation, while the M V . of PVC + 3, PVC + 2, and PVC + 1 were 26,200, 35,400, and 44,600 at same conditions. Obviously, this study is in good agreement with the functional groups and weight loss studies. PVC + 1 has the highest M V among other stabilizers, which means Ph 3 SnL (1) is the best photo-stabilizer of PVC against photo-degradation.

Calculation of the Average Molecular Weight ( ) by Utilizing Viscosity
An estimate the average molecular weight of the polymer was obtained using viscosity. Hence, the degradation causes the breaking of the polymer chain, which leads to decreasing the polymer's molecular weight [40]. The PVC solution viscosity is used to measure the . The irradiated PVC films were dissolved in the THF and the viscosity was measured using a viscometer [33]. The for each film at different irradiation times was calculated using Equation (3). Figure 5 shows the against irradiation time for the blank and additive-filled PVC. The of PVC film was reduced dramatically during the irradiation process. As a result, the for blank PVC film was approximately 170,100 at the beginning and decreased to 12,700 after 300 h of irradiation, while the of PVC + 3, PVC + 2, and PVC + 1 were 26,200, 35,400, and 44,600 at same conditions. Obviously, this study is in good agreement with the functional groups and weight loss studies. PVC + 1 has the highest among other stabilizers, which means Ph3SnL (1) is the best photo-stabilizer of PVC against photo-degradation.

Utilizing Energy Dispersive X-ray (EDX) to Examine the Photo-Stability of PVC Films
The energy dispersive X-ray (EDX) technique was utilized to analyze the elemental composition of PVC films with tin complexes after and before irradiation. Figure 6 shows the elements and EDX images of PVC films [41] that demonstrated the additives were well mixed with the polymer materials [42]. The percentage of chlorine in blank PVC is 57.9% after 300 h irradiation due to the release of hydrogen chloride molecules during irradiation. It was demonstrated that releasing of HCl for blank PVC is much higher than polymer mixes with stabilizers. Surfaces 2020, 3 FOR PEER REVIEW 9

Utilizing Energy Dispersive X-Ray (EDX) to Examine the Photo-Stability of PVC Films
The energy dispersive X-ray (EDX) technique was utilized to analyze the elemental composition of PVC films with tin complexes after and before irradiation. Figure 6 shows the elements and EDX images of PVC films [41] that demonstrated the additives were well mixed with the polymer materials [42]. The percentage of chlorine in blank PVC is 57.9% after 300 h irradiation due to the release of hydrogen chloride molecules during irradiation. It was demonstrated that releasing of HCl for blank PVC is much higher than polymer mixes with stabilizers.

Morphological Analysis of PVC Films
The morphology of the PVC surface was examined utilizing FESEM and microscope techniques. The FESEM images of the PVC surface (as shown in Figure 7) exhibited homogenous and smooth blank PVC surface before irradiation [43]. Figure 8 shows the FESEM images of blank PVC and PVC + additives after exposure to UV light. Thus, it has been demonstrated from Figure 8a that PVC surface without additives and after irradiation shows big cracks and roughness which was attributed to the breaking of polymer chains into small fragments. Another reason could be that the polymer undergoes an elimination reaction and releases HCl molecules to form alkene groups [44]. However, Figure 8b-d shows the FESEM images of the PVC films mixed with tin complexes after exposure to UV light. The PVC containing complexes' surface was smoother and had fewer cracks compared to the blank PVC after irradiation. Figure 9 shows images of the modified PVC surfaces under the microscope before and after exposure to UV light.

Morphological Analysis of PVC Films
The morphology of the PVC surface was examined utilizing FESEM and microscope techniques. The FESEM images of the PVC surface (as shown in Figure 7) exhibited homogenous and smooth blank PVC surface before irradiation [43]. Figure 8 shows the FESEM images of blank PVC and PVC + additives after exposure to UV light. Thus, it has been demonstrated from Figure 8a that PVC surface without additives and after irradiation shows big cracks and roughness which was attributed to the breaking of polymer chains into small fragments. Another reason could be that the polymer undergoes an elimination reaction and releases HCl molecules to form alkene groups [44]. However, Figure 8b-d shows the FESEM images of the PVC films mixed with tin complexes after exposure to UV light. The PVC containing complexes' surface was smoother and had fewer cracks compared to the blank PVC after irradiation. Figure 9 shows images of the modified PVC surfaces under the microscope before and after exposure to UV light.

Morphological Analysis of PVC Films
The morphology of the PVC surface was examined utilizing FESEM and microscope techniques. The FESEM images of the PVC surface (as shown in Figure 7) exhibited homogenous and smooth blank PVC surface before irradiation [43]. Figure 8 shows the FESEM images of blank PVC and PVC + additives after exposure to UV light. Thus, it has been demonstrated from Figure 8a that PVC surface without additives and after irradiation shows big cracks and roughness which was attributed to the breaking of polymer chains into small fragments. Another reason could be that the polymer undergoes an elimination reaction and releases HCl molecules to form alkene groups [44]. However, Figure 8b-d shows the FESEM images of the PVC films mixed with tin complexes after exposure to UV light. The PVC containing complexes' surface was smoother and had fewer cracks compared to the blank PVC after irradiation. Figure 9 shows images of the modified PVC surfaces under the microscope before and after exposure to UV light.

Photo-Stabilization Mechanisms
The di-and tri-organotin(IV) complexes work as photo-stabilizers for PVC films during irradiation. The three organotin complexes were synthesized for reducing PVC photo-degradation and their efficiencies follow the order 1 > 2 > 3. Such additives can stabilize PVC films depending on several mechanisms. Tin is a strong Lewis acid, so it can act as an excellent hydrochloride scavenger ( Figure 10). Tin(IV) ion can displace chlorine atom within the polymer backbone by the oxygen atoms of the carboxylate group. Such stabilizers give excellent photo-stabilizing long-term PVC by being used as secondary stabilizers [45].

Photo-stabilization Mechanisms
The di-and tri-organotin(IV) complexes work as photo-stabilizers for PVC films during irradiation. The three organotin complexes were synthesized for reducing PVC photo-degradation and their efficiencies follow the order 1 > 2 > 3. Such additives can stabilize PVC films depending on several mechanisms. Tin is a strong Lewis acid, so it can act as an excellent hydrochloride scavenger ( Figure 10). Tin(IV) ion can displace chlorine atom within the polymer backbone by the oxygen atoms of the carboxylate group. Such stabilizers give excellent photo-stabilizing long-term PVC by being used as secondary stabilizers [45]. The complexes could act as peroxide decomposers for reduced photo-degradation of PVC. The photo-oxidation of PVC produces radicals that cause the production of POOH by reacting with oxygen [46]. Thus, tin complexes can decompose peroxides (for example, hydroperoxides) ( Figure  11) [47].  Figure 12 shows the attraction between the complex (photo-stabilizer) and the polymer chain, especially the polarized C-Cl bond. This could help to stop the photo-degradation of polymer as these additives act as primary stabilizers by absorbing the UV light from the sun. The attraction between organotin(IV) and PVC can help the conversion energy of the PVC to be excited to an energy level that does not damage the polymer backbone [48]. This type of stabilizer could prevent PVC's photo-degradation by its role as free radical scavengers as shown in Figure 13. These additives might make a complex with a chromophore in an excited state [49]. Furthermore, these photo-stabilizers can absorb ultra-violet radiation straight away before it reaches the PVC and dissipate this energy to lower levels, where it does not harm the The complexes could act as peroxide decomposers for reduced photo-degradation of PVC. The photo-oxidation of PVC produces radicals that cause the production of POOH by reacting with oxygen [46]. Thus, tin complexes can decompose peroxides (for example, hydroperoxides) ( Figure 11) [47].

Photo-stabilization Mechanisms
The di-and tri-organotin(IV) complexes work as photo-stabilizers for PVC films during irradiation. The three organotin complexes were synthesized for reducing PVC photo-degradation and their efficiencies follow the order 1 > 2 > 3. Such additives can stabilize PVC films depending on several mechanisms. Tin is a strong Lewis acid, so it can act as an excellent hydrochloride scavenger ( Figure 10). Tin(IV) ion can displace chlorine atom within the polymer backbone by the oxygen atoms of the carboxylate group. Such stabilizers give excellent photo-stabilizing long-term PVC by being used as secondary stabilizers [45]. The complexes could act as peroxide decomposers for reduced photo-degradation of PVC. The photo-oxidation of PVC produces radicals that cause the production of POOH by reacting with oxygen [46]. Thus, tin complexes can decompose peroxides (for example, hydroperoxides) ( Figure  11) [47].  Figure 12 shows the attraction between the complex (photo-stabilizer) and the polymer chain, especially the polarized C-Cl bond. This could help to stop the photo-degradation of polymer as these additives act as primary stabilizers by absorbing the UV light from the sun. The attraction between organotin(IV) and PVC can help the conversion energy of the PVC to be excited to an energy level that does not damage the polymer backbone [48]. This type of stabilizer could prevent PVC's photo-degradation by its role as free radical scavengers as shown in Figure 13. These additives might make a complex with a chromophore in an excited state [49]. Furthermore, these photo-stabilizers can absorb ultra-violet radiation straight away before it reaches the PVC and dissipate this energy to lower levels, where it does not harm the  Figure 12 shows the attraction between the complex (photo-stabilizer) and the polymer chain, especially the polarized C-Cl bond. This could help to stop the photo-degradation of polymer as these additives act as primary stabilizers by absorbing the UV light from the sun. The attraction between organotin(IV) and PVC can help the conversion energy of the PVC to be excited to an energy level that does not damage the polymer backbone [48].

Photo-stabilization Mechanisms
The di-and tri-organotin(IV) complexes work as photo-stabilizers for PVC films during irradiation. The three organotin complexes were synthesized for reducing PVC photo-degradation and their efficiencies follow the order 1 > 2 > 3. Such additives can stabilize PVC films depending on several mechanisms. Tin is a strong Lewis acid, so it can act as an excellent hydrochloride scavenger ( Figure 10). Tin(IV) ion can displace chlorine atom within the polymer backbone by the oxygen atoms of the carboxylate group. Such stabilizers give excellent photo-stabilizing long-term PVC by being used as secondary stabilizers [45]. The complexes could act as peroxide decomposers for reduced photo-degradation of PVC. The photo-oxidation of PVC produces radicals that cause the production of POOH by reacting with oxygen [46]. Thus, tin complexes can decompose peroxides (for example, hydroperoxides) ( Figure  11) [47].  Figure 12 shows the attraction between the complex (photo-stabilizer) and the polymer chain, especially the polarized C-Cl bond. This could help to stop the photo-degradation of polymer as these additives act as primary stabilizers by absorbing the UV light from the sun. The attraction between organotin(IV) and PVC can help the conversion energy of the PVC to be excited to an energy level that does not damage the polymer backbone [48]. This type of stabilizer could prevent PVC's photo-degradation by its role as free radical scavengers as shown in Figure 13. These additives might make a complex with a chromophore in an excited state [49]. Furthermore, these photo-stabilizers can absorb ultra-violet radiation straight away before it reaches the PVC and dissipate this energy to lower levels, where it does not harm the This type of stabilizer could prevent PVC's photo-degradation by its role as free radical scavengers as shown in Figure 13. These additives might make a complex with a chromophore in an excited state [49]. Furthermore, these photo-stabilizers can absorb ultra-violet radiation straight away before it reaches the PVC and dissipate this energy to lower levels, where it does not harm the chemical structure of the polymer chains due to the photo-stabilizer conjugation system that absorbs the UV [50]. chemical structure of the polymer chains due to the photo-stabilizer conjugation system that absorbs the UV [50].

Conclusions
Three Organotin complexes, numbered 1-3, were synthesized from the reaction of di-and tri-organotin chlorides and Ibuprofen and used as photo-stabilizers for the PVC. These additives showed their efficiency to decrease the photo-degradation of PVC films by using various analyzing methods. These methods showed a significant reduction in the PVC films' photo-degradation and monitored the certain functional groups' growth of carbonyl (IC=O) and polyene (IC=C) upon the time of irradiation (300 h), percentage of weight loss, and changes on the surface of PVC films in the presence and absence of additives. Organotin(IV) complexes stabilize the PVC films by different mechanisms, such as HCl scavenger, primary stabilizers, and peroxide decomposers. The photo-stabilization impact on PVC followed the order of: 1 > 2 > 3 > PVC (blank). The Ph3SnL complex was the most effective complex as a photo-stabilizer for PVC films according to several mechanisms.

Conclusions
Three Organotin complexes, numbered 1-3, were synthesized from the reaction of di-and tri-organotin chlorides and Ibuprofen and used as photo-stabilizers for the PVC. These additives showed their efficiency to decrease the photo-degradation of PVC films by using various analyzing methods. These methods showed a significant reduction in the PVC films' photo-degradation and monitored the certain functional groups' growth of carbonyl (I C=O ) and polyene (I C=C ) upon the time of irradiation (300 h), percentage of weight loss, and changes on the surface of PVC films in the presence and absence of additives. Organotin(IV) complexes stabilize the PVC films by different mechanisms, such as HCl scavenger, primary stabilizers, and peroxide decomposers. The photo-stabilization impact on PVC followed the order of: 1 > 2 > 3 > PVC (blank). The Ph 3 SnL complex was the most effective complex as a photo-stabilizer for PVC films according to several mechanisms.